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Publications

Below is a list of publications that have either produced samples and data available at the NIMH Repository, or utilized samples or data accessed through the NIMH Repository. Publications are sorted by disease category and date.

Attention-Deficit Hyperactivity Disorder

Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PM, Li Q, Hakonarson H

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genome Medicine 2017; 9:106.

Richards Jennifer S, Arias Vásquez Alejandro, van Rooij Daan, van der Meer Dennis, Franke Barbara, Hoekstra Pieter J, Heslenfeld Dirk J, Oosterlaan Jaap, Faraone Stephen V, Hartman Catharina A, Buitelaar Jan K

Testing differential susceptibility: Plasticity genes, the social environment, and their interplay in adolescent response inhibition.

The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2017; 18(4):308-321.

van der Meer Dennis, Hartman Catharina A, van Rooij Daan, Franke Barbara, Heslenfeld Dirk J, Oosterlaan Jaap, Faraone Stephen V, Buitelaar Jan K, Hoekstra Pieter J

Effects of dopaminergic genes, prenatal adversities, and their interaction on attention-deficit/hyperactivity disorder and neural correlates of response inhibition.

Journal of psychiatry & neuroscience : JPN 2017; 42(2):113-121.

Richards JS, Arias Vásquez A, Franke B, Hoekstra PJ, Heslenfeld DJ, Oosterlaan J, Faraone SV, Buitelaar JK, Hartman CA

Developmentally Sensitive Interaction Effects of Genes and the Social Environment on Total and Subcortical Brain Volumes

PLoS ONE 2016; 11(5):e0155755.

Richards Jennifer S, Hartman Catharina A, Franke Barbara, Hoekstra Pieter J, Heslenfeld Dirk J, Oosterlaan Jaap, Arias Vásquez Alejandro, Buitelaar Jan K

Differential susceptibility to maternal expressed emotion in children with ADHD and their siblings? Investigating plasticity genes, prosocial and antisocial behaviour.

European child & adolescent psychiatry 2015; 24(2):209-17.

Zuo L, Saba L, Lin X, Tan Y, Wang K, Krystal JH, Tabakoff B, Luo X

Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2015; 168(7):544-556.

Richards JS, Hartman CA, Franke B, Hoekstra PJ, Heslenfeld DJ, Oosterlaan J, Vásquez AA, Buitelaar JK

Differential Susceptibility to Maternal Expressed Emotion in Children with ADHD and their Siblings? Investigating Plasticity Genes, Prosocial and Antisocial Behaviour

European child & adolescent psychiatry 2014; 24(2):209-217.

van der Meer D, Hartman CA, Richards J, Bralten JB, Franke B, Oosterlaan J, Heslenfeld DJ, Faraone SV, Buitelaar JK, Hoekstra PJ

The serotonin transporter gene polymorphism 5-HTTLPR moderates the effects of stress on attention-deficit/hyperactivity disorder

Journal of child psychology and psychiatry, and allied disciplines 2014; 55(12):1363-1371.

van der Meer Dennis, Hartman Catharina A, Richards Jennifer, Bralten Janita B, Franke Barbara, Oosterlaan Jaap, Heslenfeld Dirk J, Faraone Stephen V, Buitelaar Jan K, Hoekstra Pieter J

The serotonin transporter gene polymorphism 5-HTTLPR moderates the effects of stress on attention-deficit/hyperactivity disorder.

Journal of child psychology and psychiatry, and allied disciplines 2014; 55(12):1363-71.

Greenwood TA, Joo EJ, Shektman T, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR

Association of Dopamine Transporter Gene Variants with Childhood ADHD Features in Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 0(2):137-145.

Wang KS, Liu X, Zhang Q, Aragam N, Pan Y

Parent-of-origin effects of FAS and PDLIM1 in attention-deficit/hyperactivity disorder

Journal of Psychiatry & Neuroscience : JPN 2012; 37(1):46-52.

Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, Frackelton EC, Chiavacci RM, Sakurai T, Rabin C, Middleton FA, Thomas KA, Garris M, Mentch F, Freitag CM, Steinhausen HC, Todorov AA, Reif A, Rothenberger A, Franke B, Mick EO, Roeyers H, Buitelaar J, Lesch KP, Banaschewski T, Ebstein RP, Mulas F, Oades RD, Sergeant J, Sonuga-Barke E, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Meyer J, Pálmason H, Seitz C, Loo SK, Smalley SL, Biederman J, Kent L, Asherson P, Anney RJ, Gaynor JW, Shaw P, Devoto M, White PS, Grant SF, Buxbaum JD, Rapoport JL, Williams NM, Nelson SF, Faraone SV, Hakonarson H

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Nature genetics 2011; 44(1):78-84.

Müller UC, Asherson P, Banaschewski T, Buitelaar JK, Ebstein RP, Eisenberg J, Gill M, Manor I, Miranda A, Oades RD

The impact of study design and diagnostic approach in a large multi-centre ADHD study. Part 1: ADHD symptom patterns

BMC psychiatry 2011; 11(1):54.

Sonuga-Barke Edmund J S, Kumsta Robert, Schlotz Wolff, Lasky-Su Jessica, Marco Rafaela, Miranda Ana, Mulas Fernando, Oades Robert D, Banaschewski Tobias, Mueller Ueli, Andreou Penny, Christiansen Hanna, Gabriels Isabel, Uebel Henrik, Kuntsi Jonna, Franke Barbara, Buitelaar Jan, Ebstein Richard, Gill Michael, Anney Richard, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Steinhausen Hans Christoph, Asherson Philip, Faraone Stephen V

A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.

Biological psychiatry 2011; 70(3):230-6.

Sonuga-Barke EJ, Kumsta R, Schlotz W, Lasky-Su J, Marco R, Miranda A, Mulas F, Oades RD, Banaschewski T, Mueller U, Andreou P, Christiansen H, Gabriels I, Uebel H, Kuntsi J, Franke B, Buitelaar J, Ebstein R, Gill M, Anney R, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Asherson P, Faraone SV

A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in ADHD boys and siblings

Biological psychiatry 2011; 70(3):230-236.

Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P S

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.

Molecular psychiatry 2010; 15(6):637-46.

Joo EJ, Greenwood TA, Schork N, McKinney RA, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR

Suggestive evidence for linkage of ADHD features in bipolar disorder to chromosome 10p14

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 153(1):260-268.

Lasky-Su J, Won S, Mick E, Anney RJ, Franke B, Neale B, Biederman J, Smalley SL, Loo SK, Todorov A, Faraone SV, Weiss ST, Lange C

On Genome-wide Association Studies for Family-Based Designs: An Integrative Analysis Approach Combining Ascertained Family Samples with Unselected Controls

American Journal of Human Genetics 2010; 86(4):573-580.

Neale Benjamin M, Medland Sarah E, Ripke Stephan, Asherson Philip, Franke Barbara, Lesch Klaus-Peter, Faraone Stephen V, Nguyen Thuy Trang, Schäfer Helmut, Holmans Peter, Daly Mark, Steinhausen Hans-Christoph, Freitag Christine, Reif Andreas, Renner Tobias J, Romanos Marcel, Romanos Jasmin, Walitza Susanne, Warnke Andreas, Meyer Jobst, Palmason Haukur, Buitelaar Jan, Vasquez Alejandro Arias, Lambregts-Rommelse Nanda, Gill Michael, Anney Richard J L, Langely Kate, O'Donovan Michael, Williams Nigel, Owen Michael, Thapar Anita, Kent Lindsey, Sergeant Joseph, Roeyers Herbert, Mick Eric, Biederman Joseph, Doyle Alysa, Smalley Susan, Loo Sandra, Hakonarson Hakon, Elia Josephine, Todorov Alexandre, Miranda Ana, Mulas Fernando, Ebstein Richard P, Rothenberger Aribert, Banaschewski Tobias, Oades Robert D, Sonuga-Barke Edmund, McGough James, Nisenbaum Laura, Middleton Frank, Hu Xiaolan, Nelson Stan

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.

Journal of the American Academy of Child and Adolescent Psychiatry 2010; 49(9):884-97.

Nijmeijer Judith S, Arias-Vásquez Alejandro, Rommelse Nanda N J, Altink Marieke E, Anney Richard J L, Asherson Philip, Banaschewski Tobias, Buschgens Cathelijne J M, Fliers Ellen A, Gill Michael, Minderaa Ruud B, Poustka Luise, Sergeant Joseph A, Buitelaar Jan K, Franke Barbara, Ebstein Richard P, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sonuga-Barke Edmund J S, Steinhausen Hans-Christoph, Faraone Stephen V, Hartman Catharina A, Hoekstra Pieter J

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.

Journal of the American Academy of Child and Adolescent Psychiatry 2010; 49(7):675-85.

Rizzi TS, Arias-Vasquez A, Rommelse N, Kuntsi J, Anney R, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Ruano D, Van der Sluis S, Markunas CA, Garrett ME, Ashley-Koch AE, Kollins SH, Anastopoulos AD, Hansell NK, Wright MJ, Montgomery GW, Martin NG, Harris SE, Davies G, Tenesa A, Porteous DJ, Starr JM, Deary IJ, St. Pourcain B, Smith GD, Timpson NJ, Evans DM, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Franke B, Posthuma D

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

American Journal of Medical Genetics 2010; 156(2):145-157.

Ruano D, Abecasis GR, Glaser B, Lips ES, Cornelisse LN, de Jong AP, Evans DM, Smith GD, Timpson NJ, Smit AB, Heutink P, Verhage M, Posthuma D

Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability

American Journal of Human Genetics 2010; 86(2):113-125.

Altink ME, Slaats-Willemse DI, Rommelse NN, Buschgens CJ, Fliers EA, Arias-Vásquez A, Xu X, Franke B, Sergeant JA, Faraone SV, Buitelaar JK

Effects of maternal and paternal smoking on attentional control in children with and without ADHD

European Child & Adolescent Psychiatry 2009; 18(8):465-475.

Anney RJ, Kenny E, O'Dushlaine CT, Lasky-Su J, Franke B, Morris DW, Neale BM, Asherson P, Faraone SV, Gill M

Non-Random Error in Genotype Calling Procedures: implications for family-based and case-control genome-wide association studies

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008; 147B(8):1379-1386.

Neale Benjamin M, Lasky-Su Jessica, Anney Richard, Franke Barbara, Zhou Kaixin, Maller Julian B, Vasquez Alejandro Arias, Asherson Philip, Chen Wai, Banaschewski Tobias, Buitelaar Jan, Ebstein Richard, Gill Michael, Miranda Ana, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Steinhausen Hans Christoph, Sonuga-Barke Edmund, Mulas Fernando, Taylor Eric, Laird Nan, Lange Christoph, Daly Mark, Faraone Stephen V

Genome-wide association scan of attention deficit hyperactivity disorder.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008; 147B(8):1337-44.

Neale BM, Su J, Anney R, Franke B, Zhou K, Maller JB, Vasquez AA, Asherson P, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Sonuga-Barke E, Mulas F, Taylor E, Laird N, Lange C, Daly M, Faraone SV

Genome-wide Association Scan of Attention Deficit Hyperactivity Disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008; 147B(8):1337-1344.

Oades Robert D, Lasky-Su Jessica, Christiansen Hanna, Faraone Stephen V, Sonuga-Barke Edmund Js, Banaschewski Tobias, Chen Wai, Anney Richard Jl, Buitelaar Jan K, Ebstein Richard P, Franke Barbara, Gill Michael, Miranda Ana, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph A, Steinhausen Hans-Christoph, Taylor Eric A, Thompson Margaret, Asherson Philip

The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis.

Behavioral and brain functions : BBF 2008; 4:48.

Zhou Kaixin, Asherson Philip, Sham Pak, Franke Barbara, Anney Richard J L, Buitelaar Jan, Ebstein Richard, Gill Michael, Brookes Keeley, Buschgens Cathelijne, Campbell Desmond, Chen Wai, Christiansen Hanna, Fliers Ellen, Gabriëls Isabel, Johansson Lena, Marco Rafaela, Mulas Fernando, Müller Ueli, Mulligan Aisling, Neale Benjamin M, Rijsdijk Fruhling, Rommelse Nanda, Uebel Henrik, Psychogiou Lamprini, Xu Xiaohui, Banaschewski Tobias, Sonuga-Barke Edmund, Eisenberg Jacques, Manor Iris, Miranda Ana, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Steinhausen Hans-Christoph, Taylor Eric, Thompson Margaret, Faraone Stephen V

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.

Biological psychiatry 2008; 64(7):571-6.

Zhou K, Asherson P, Sham P, Franke B, Anney RJ, Buitelaar J, Ebstein R, Gill M, Brookes K, Buschgens C, Campbell D, Chen W, Christiansen H, Fliers E, Gabriëls I, Johansson L, Marco R, Mulas F, Müller U, Mulligan A, Neale BM, Rijsdijk F, Rommelse N, Uebel H, Psychogiou L, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV

Linkage to Chromosome 1p36 for Attention Deficit Hyperactivity Disorder Traits in School and Home Settings

Biological psychiatry 2008; 64(7):571-576.

Kuntsi Jonna, Neale Benjamin M, Chen Wai, Faraone Stephen V, Asherson Philip

The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

Behavioral and brain functions : BBF 2006; 2:27.

Alzheimer's Disease

Hu B, Won H, Mah W, Park RB, Kassim B, Spiess K, Kozlenkov A, Crowley CA, Pochareddy S, Li Y, Dracheva S, Sestan N, Akbarian S, Geschwind DH

Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

Nature Communications 2021; 12:3968.

Ramos EM, Dokuru DR, Van Berlo V, Wojta K, Wang Q, Huang AY, Miller ZA, Karydas AM, Bigio EH, Rogalski E, Weintraub S, Rader B, Miller BL, Gorno-Tempini ML, Mesulam MM, Coppola G

Genetic screen in a large series of patients with primary progressive aphasia

Alzheimer's & dementia : the journal of the Alzheimer's Association 2019; 15(4):553-560.

DeMichele-Sweet MA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, Lopez OL, Sibille EL, Kamboh MI, Devlin B, Sweet RA

Genetic Risk for Schizophrenia and Psychosis in Alzheimer Disease

Molecular psychiatry 2017; 10.1038/mp.2017.81.

Alfonso SI, Callender JA, Hooli B, Antal CE, Mullin K, Sherman MA, Lesné SE, Leitges M, Newton AC, Tanzi RE, Malinow R

Gain-of-function mutations in protein kinase Cα (PKCα) may promote synaptic defects in Alzheimer's disease

Science signaling 2016; 9(427):ra47.

Bettayeb K, Hooli BV, Parrado AR, Randolph L, Varotsis D, Aryal S, Gresack J, Tanzi RE, Greengard P, Flajolet M

Relevance of the COPI complex for Alzheimer's disease progression in vivo

Proceedings of the National Academy of Sciences 2016; 201604176.

Bettayeb K, Hooli BV, Parrado AR, Randolph L, Varotsis D, Aryal S, Gresack J, Tanzi RE, Greengard P, Flajolet M

Relevance of the COPI complex for Alzheimer's disease progression in vivo

Proceedings of the National Academy of Sciences of the United States of America 2016; 113(19):5418-5423.

Saad M, Brkanac Z, Wijsman EM

Family-based Genome Scan for Age at Onset of Late Onset Alzheimer's Disease in Whole Exome Sequencing Data

Genes, brain, and behavior 2015; 14(8):607-617.

Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Gonzalez Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, Tschanz JT, Munger RG, Corcoran CD, Rogaeva E, Lin CF, Dombroski BA, Cantwell LB, Partch A, Valladares O, Hakonarson H, St George-Hyslop P, Green RC, Goate AM, Foroud TM, Carney RM, Larson EB, Behrens TW, Kauwe JS, Haines JL, Farrer LA, Pericak-Vance MA, Mayeux R, Schellenberg GD

Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States

JAMA neurology 2015; 72(2):209-216.

DeMichele-Sweet MA, Sweet RA

Genetics of Psychosis in Alzheimer Disease

Current genetic medicine reports 2014; 2(1):30-38.

Hooli BV, Kovacs-Vajna ZM, Mullin K, Blumenthal MA, Mattheisen M, Zhang C, Lange C, Mohapatra G, Bertram L, Tanzi RE

Rare autosomal copy number variations in early-onset familial Alzheimer's disease

Molecular psychiatry 2014; 19(6):676-681.

Hooli BV, Parrado AR, Mullin K, Yip WK, Liu T, Roehr JT, Qiao D, Jessen F, Peters O, Becker T

The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk

Neurology 2014; 83(15):1353-1358.

Wang R, Halper-Stromberg E, Szymanski-Pierce M, Bassett S, Avramopoulos D

Genetic determinants of neuroglobin transcription

Neurogenetics 2014; 15(1):65-75.

Schafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA

Genomics 2013; 102(4):270-277.

Cai G, Atzmon G, Naj A, Beecham GW, Barzilai N, Haines JL, Sano M, Pericak-Vance MA, Buxbaum JD

Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer Disease

Neurobiol Aging 2012; 33(2):416-417.

Hooli BV, Mohapatra G, Mattheisen M, Parrado AR, Roehr JT, Shen Y, Gusella JF, Moir R, Saunders AJ, Lange C, Tanzi RE, Bertram L

Role of common and rare APP DNA sequence variants in Alzheimer disease

Neurology 2012; 78(16):1250-1257.

Majounie E, Abramzon Y, Renton AE, Perry R, Bassett SS, Pletnikova O, Troncoso JC, Hardy J, Singleton AB, Traynor BJ

Repeat Expansion in C9ORF72 in Alzheimer's Disease

The New England journal of medicine 2012; 366(3):283-284.

Choi Y, Marchani EE, Bird TD, Steinbart EJ, Blacker D, Wijsman EM

Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2011; 156(7):785-798.

Brown AM, Finch SJ, Gordon D

Genome-wide association study of genetic loci and Alzheimer disease

JAMA 2010; 304(8):858-858.

Fallin MD, Szymanski M, Wang R, Gherman A, Bassett SS, Avramopoulos D

Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls

Neurogenetics 2010; 11(3):335-348.

Gianni D, Li A, Tesco G, McKay KM, Moore J, Raygor K, Rota M, Gwathmey JK, Dec GW, Aretz T, Leri A, Semigran MJ, Anversa P, Macgillivray TE, Tanzi RE, Monte FD

Protein Aggregates and Novel Presenilin Gene Variants in Idiopathic Dilated Cardiomyopathy

Circulation 2010; 121(10):1216-1226.

Butler AW, Ng MYM, Hamshere ML, Forabosco P, Wroe R, Al-Chalabi A, Lewis CM, Powell JF

Meta-analysis of linkage studies for Alzheimer's disease-a web resource

Neurobiology of aging 2009; 30(7):1037-1047.

Kim M, Suh J, Romano D, Truong MH, Mullin K, Hooli B, Norton D, Tesco G, Elliott K, Wagner SL, Moir RD, Becker KD, Tanzi RE

Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate α-secretase activity

Human Molecular Genetics 2009; 18(20):3987-3996.

Schjeide BM, McQueen MB, Mullin K, DiVito J, Hogan MF, Parkinson M, Hooli B, Lange C, Blacker D, Tanzi RE, Bertram L

Assessment of Alzheimer's disease case-control associations using family-based methods

Neurogenetics 2009; 10(1):19-25.

Schjeide BM, Hooli B, Parkinson M, Hogan MF, DiVito J, Mullin K, Blacker D, Tanzi RE, Bertram L

GAB2 as an Alzheimer Disease Susceptibility Gene: Follow-up of Genomewide Association Results

Archives of neurology 2009; 66(2):250-254.

Bertram L, Lange C, Mullin K, Parkinson M, Hsiao M, Hogan MF, Schjeide BM, Hooli B, DiVito J, Ionita I, Jiang H, Laird N, Moscarillo T, Ohlsen KL, Elliott K, Wang X, Hu-Lince D, Ryder M, Murphy A, Wagner SL, Blacker D, Becker KD, Tanzi RE

Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE

American Journal of Human Genetics 2008; 83(5):623-632.

Blom ES, Holmans P, Arepalli S, Adighibe O, Hamshere ML, Gatz M, Pedersen NL, Bergem AL, Owen MJ, Hollingworth P, Goate A, Williams J, Lannfelt L, Hardy J, Wavrant-De Vrièze F, Glaser A

Does APOE Explain the Linkage of Alzheimer's Disease to Chromosome 19q13?

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(6):778-783.

Chen Z, Simmons MS, Perry RT, Wiener HW, Harrell LE, Go RCP

Genetic association of neurotrophic tyrosine kinase receptor type 2 (NTRK2) With Alzheimer's disease

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147(3):363-369.

Dickson MR, Li J, Wiener HW, Perry RT, Blacker D, Bassett SS, Go RC

A Genomic Scan for Age at Onset of Alzheimer's Disease in 437 Families From the NIMH Genetic Initiative

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(6):784-792.

Profenno LA, Faraone SV

Diabetes and overweight associate with non-APOE4 genotype in an alzheimer's disease population

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147(6):822-829.

Schaffer BA, Bertram L, Miller BL, Mullin K, Weintraub S, Johnson N, Bigio EH, Mesulam M, Wiedau-Pazos M, Jackson GR, Cummings JL, Cantor RM, Levey AI, Tanzi RE, Geschwind DH

Association of GSK3B With Alzheimer Disease and Frontotemporal Dementia

Archives of neurology 2008; 65(10):1368-1374.

Thornton-Wells TA, Moore JH, Martin ER, Pericak-Vance MA, Haines JL

Confronting Complexity in Late-Onset Alzheimer Disease: Application of Two-Stage Analysis Approach Addressing Heterogeneity and Epistasis

Genetic epidemiology 2008; 32(3):187-203.

Bertram L, Hsiao M, McQueen MB, Parkinson M, Mullin K, Blacker D, Tanzi RE

The LDLR locus in Alzheimer's disease: a family-based study and meta-analysis of case-control data

Neurobiology of aging 2007; 28(1):18. e1-18. e4.

Bertram L, Mullin K, Parkinson M, Hsiao M, Moscarillo TJ, Wagner SL, Becker KD, Velicelebi G, Blacker D, Tanzi RE

Is α-T catenin (VR22) an Alzheimer's disease risk gene?

Journal of Medical Genetics 2007; 44(1):e63.

Brown AM, Gordon D, Lee H, Wavrant-De Vrièze F, Cellini E, Bagnoli S, Nacmias B, Sorbi S, Hardy J, Blass JP

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations

Neurochemical research 2007; 32(4-5):857-869.

De Ferrari GV, Papassotiropoulos A, Biechele T, De-Vrieze FW, Avila ME, Major MB, Myers A, Sáez K, Henríquez JP, Zhao A

Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease

Proceedings of the National Academy of Sciences 2007; 104(22):9434-9439.

Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A

Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease

Human molecular genetics 2007; 16(22):2703-2712.

Ismail MS, Dagerman K, Tariot PN, Abbott S, Kavanaugh S, Schneider LS

National Institute of Mental Health Clinical Antipsychotic Trials of Intervention Effectiveness-Alzheimer's Disease (CATIE-AD): baseline characteristics

Curr Alzheimer Res 2007; 4(3):325-335.

Perry RT, Wiener H, Harrell LE, Blacker D, Tanzi RE, Bertram L, Bassett SS, Go RCP

Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(2):220-227.

Wavrant-De Vrièze F, Compton D, Womick M, Arepalli S, Adighibe O, Li L, Pérez-Tur J, Hardy J

ABCA1 polymorphisms and Alzheimer's disease

Neuroscience letters 2007; 416(2):180-183.

Wiener HW, Perry RT, Chen Z, Harrell LE, Go RCP

A polymorphism in SOD2 is associated with development of Alzheimer's disease

Genes, Brain and Behavior 2007; 6(8):770-776.

Adighibe O, Arepalli S, Duckworth J, Hardy J, Wavrant-De Vrièze F

Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease

Neurobiology of aging 2006; 27(10):1431-1434.

Avramopoulos D, Zandi P, Gherman A, Fallin MD, Bassett SS

Testing groups of genomic locations for enrichment in disease loci using linkage scan data: A method for hypothesis testing

Human Genomics 2006; 2(6):345-352.

Bassett SS, Avramopoulos D, Perry RT, Wiener H, Watson B Jr, Go RC, Fallin MD

Further evidence of a maternal parent-of-origin effect on chromosome 10 in late-onset Alzheimer's disease

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2006; 141B(5):537-540.

Bassett SS, Yousem DM, Cristinzio C, Kusevic I, Yassa MA, Caffo BS, Zeger SL

Familial risk for Alzheimer's disease alters fMRI activation patterns

Brain 2006; 129(5):1229-1239.

Bertram L, Hsiao M, Lange C, Blacker D, Tanzi RE

Single-Nucleotide Polymorphism rs498055 on Chromosome 10q24 Is Not Associated with Alzheimer Disease in Two Independent Family Samples

American Journal of Human Genetics 2006; 79(1):180-183.

Grupe Andrew, Li Yonghong, Rowland Charles, Nowotny Petra, Hinrichs Anthony L, Smemo Scott, Kauwe John S K, Maxwell Taylor J, Cherny Sara, Doil Lisa, Tacey Kristina, van Luchene Ryan, Myers Amanda, Wavrant-De Vrièze Fabienne, Kaleem Mona, Hollingworth Paul, Jehu Luke, Foy Catherine, Archer Nicola, Hamilton Gillian, Holmans Peter, Morris Chris M, Catanese Joseph, Sninsky John, White Thomas J, Powell John, Hardy John, O'Donovan Michael, Lovestone Simon, Jones Lesley, Morris John C, Thal Leon, Owen Michael, Williams Julie, Goate Alison

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

American journal of human genetics 2006; 78(1):78-88.

Li YJ, Scott WK, Zhang L, Lin PI, Oliveira SA, Skelly T, Doraiswamy MP, Welsh-Bohmer KA, Martin ER, Haines JL, Pericak-Vance MA, Vance JM

Revealing the role of Glutathione S-Transferase Omega in age at onset of Alzheimer and Parkinson Diseases

Neurobiology of aging 2006; 27(8):1087-1093.

Lin PI, Martin ER, Browning-Large CA, Schmechel DE, Welsh-Bohmer KA, Doraiswamy PM, Gilbert JR, Haines JL, Pericak-Vance MA

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis

Neurogenetics 2006; 7(3):157-165.

McQueen MB, Blacker D, Laird NM

Variance Calculations for Identity-by-Descent Estimation

American Journal of Human Genetics 2006; 78(6):914-921.

Avramopoulos D, Fallin MD, Bassett SS

Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 132(1):9-13.

Bacanu SA, Devlin B, Chowdari KV, DeKosky ST, Nimgaonkar VL, Sweet RA

Heritability of psychosis in Alzheimer disease

The American journal of geriatric psychiatry 2005; 13(7):624-627.

Bertram L, Hiltunen M, Parkinson M, Ingelsson M, Lange C, Ramasamy K, Mullin K, Menon R, Sampson AJ, Hsiao MY

Family-based association between Alzheimer's disease and variants in UBQLN1

New England Journal of Medicine 2005; 352(9):884-894.

Dickson MR, Perry RT, Wiener H, Go RCP

Association studies of transforming growth factor-β1 and Alzheimer's disease

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 139(1):38-41.

Go RCP, Perry RT, Wiener H, Bassett SS, Blacker D, Devlin B, Sweet RA

Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 139(1):28-32.

Holmans P, Hamshere M, Hollingworth P, Rice F, Tunstall N, Jones S, Moore P, DeVrieze FW, Myers A, Crook R

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 135(1):24-32.

Lahiri DK, Ge YW, Maloney B, Wavrant-De Vrièze F, Hardy J

Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease

Neurobiology of aging 2005; 26(10):1329-1341.

Bertram L, Parkinson M, Mullin K, Menon R, Blacker D, Tanzi R

No association between a previously reported OLR1 3' UTR polymorphism and Alzheimer's disease in a large family sample

Journal of Medical Genetics 2004; 41(4):286-288.

Busby V, Goossens S, Nowotny P, Hamilton G, Smemo S, Myers A, Womick M, Woo D, Compton D, Al-Sarej S, Killick R, Pickering-Brown S, Lendon C, Iwatsubo T, Morris JC, Norton J, Mann D, Janssens B, Hardy J, O'Donovan M, Jones L, Williams J, Holmans P, Owen MJ, Grupe A, Powell J, van Hengel J, Goate A, van Roy F, Lovestone S

Alpha-T-catenin is expressed in human brain and interacts with the want signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

Neuromolecular Med 2004; 5:133-146.

Ghosh S, Reich T

The Sib TDT adjusted for age of disease onset

Annals of human genetics 2004; 68(3):249-256.

Kamboh MI

Molecular genetics of late-onset Alzheimer's disease

Annals of human genetics 2004; 68(4):381-404.

Li Y, Nowotny P, Holmans P, Smemo S, Kauwe J, Hinrichs T, Tacey K, Doil L, van Luchene R, Garcia V, Rowland C, Schrodi S, Leong D, Gogic G, Chan J, Cravchik A, Ross D, Lau K, Kwok S, Chang S-Y, Catanese J, Sninsky J, White T, Hardy J, Powell J, Lovestone S, Morris JC, Thal L, Owen M, Williams J, Goate A, Grupe A

Association of late onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

PNAS 2004; 101:15688-15693.

Myers AJ, Marshall H, Holmans P, Compton D, Crook RJP, Mander AP, Nowotny P, Smemo S, Dunstan M, Jehu L

Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 124(1):29-37.

Nicodemus KK, Stenger JE, Schmechel DE, Welsh-Bohmer KA, Saunders AM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA

Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease

Neurogenetics 2004; 5(4):201-208.

Blacker D, Bertram L, Saunders AJ, Moscarillo TJ, Albert MS, Wiener H, Perry RT, Collins JS, Harrell LE, Go RCP

Results of a high-resolution genome screen of 437 Alzheimer's disease families

Human Molecular Genetics 2003; 12(1):23-32.

Saunders AJ, Bertram L, Mullin K, Sampson AJ, Latifzai K, Basu S, Jones J, Kinney D, MacKenzie-Ingano L, Yu S

Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin

Human molecular genetics 2003; 12(21):2765-2776.

Schneider LS, Ismail MS, Dagerman K, Davis S, Olin, McManus D, Pfeiffer E, Ryan JM, Sultzer DL, Tariot PN

Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE): Alzheimer's disease trial

Schizophr Bull 2003; 29(1):57-72.

Scott WK, Hauser ER, Schmechel DE, Welsh-Bohmer KA, Small GW, Roses AD, Saunders AM, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA

Ordered-Subsets Linkage Analysis Detects Novel Alzheimer Disease Loci on Chromosomes 2q34 and 15q22

American Journal of Human Genetics 2003; 73(5):1041-1051.

Sweet RA, Nimgaonkar VL, Devlin B, Jeste DV

Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype

Molecular psychiatry 2003; 8(4):383-392.

Bacanu SA, Devlin B, Chowdari KV, DeKosky ST, Nimgaonkar VL, Sweet RA

Linkage analysis of Alzheimer disease with psychosis

Neurology 2002; 59(1):118-120.

Devlin B, Bacanu SA, Jones BL, Roeder K

Reply to Olson

Genetic Epidemiology 2002; 23(4):449-455.

Myers A, Wavrand De Frieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstal N, Jones L, Lovestone S, Williams J, Owen M, Hardy J, Goate A

A full genome screen for Alzheimer's disease: Stage II analysis

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2002; 114:235-244.

Poduslo SE, Shook B, Drigalenko E, Yin X

Lack of association of the two polymorphisms in alpha-2 macroglobulin with Alzheimer disease

American journal of medical genetics 2002; 110(1):30-35.

Sweet RA, Nimgaonkar VL, Devlin B, Lopez OL, DeKosky ST

Increased familial risk of the psychotic phenotype of Alzheimer disease

Neurology 2002; 58(6):907-911.

Bertram L, Guénette S, Jones J, Keeney D, Mullin K, Crystal A, Basu S, Yhu S, Deng A, Rebeck GW

No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease

Annals of neurology 2001; 49(1):114-116.

Bertram L, Tanzi RE

Dancing in the dark?

Journal of Molecular Neuroscience 2001; 17(2):127-136.

Curtis D, North BV, Sham PC

A novel method of two-locus linkage analysis applied to a genome scan for late onset Alzheimer's disease

Annals of human genetics 2001; 65(5):473-482.

Horvath S, Xu X, Laird NM

The family based association test method: strategies for studying general genotype-phenotype associations.

European Journal of Human Genetics 2001; 9(4):.

Lendon C, Craddock N

Susceptibility gene (s) for Alzheimer's disease on chromosome 10

TRENDS in Neurosciences 2001; 24(10):557-559.

Mokliatchouk O, Blacker D, Rabinowitz D

Association tests for traits with variable age at onset

Human Heredity 2001; 51(1-2):46-53.

Olson JM, Goddard KA, Dudek DM

The Amyloid Precursor Protein Locus and Very-Late-Onset Alzheimer Disease

American Journal of Human Genetics 2001; 69(4):895-899.

Poduslo SE, Yin X

Chromosome 12 and late-onset Alzheimer's disease

Neuroscience letters 2001; 310(2):188-190.

Qu T, Manev R, Manev H

5-Lipoxygenase (5-LOX) promoter polymorphism in patients with early-onset and late-onset Alzheimer's disease

The Journal of neuropsychiatry and clinical neurosciences 2001; 13(2):304-305.

Schneider LS, Tariot PN, Lyketsos CG, Dagerman KS, Davis KL, Davis S, Hsiao JK, Jeste DV, Katz IR, Olin JT, Pollock BG, Rabins PV, Rosenheck RA, Small GW, Lebowitz B, Lieberman JA

National Institute of Mental Health Clinical Antipsychotic Trials of Intervention Effectiveness CATIE-AD): Alzheimer disease trial methodology

Am J Geriatr Psychiatry 2001; 9(4):346-360.

Bertram L, Blacker D, Crystal A, Mullin K, Keeney D, Jones J, Basu S, Yhu S, Guenette S, McInnis M

Candidate genes showing no evidence for association or linkage with Alzheimer's disease using family-based methodologies

Experimental gerontology 2000; 35(9):1353-1361.

Collins JS, Perry RT, Watson B, Harrell LE, Acton RT, Blacker D, Albert MS, Tanzi RE, Bassett SS, McInnis MG

Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative

American journal of medical genetics 2000; 96(6):823-830.

Guénette SY, Bertram L, Crystal A, Bakondi B, Hyman BT, Rebeck GW, Tanzi RE, Blacker D

Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients

Neuroscience letters 2000; 296(1):17-20.

Lake SL, Blacker D, Laird NM

Family-Based Tests of Association in the Presence of Linkage

American Journal of Human Genetics 2000; 67(6):1515-1525.

Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R

Susceptibility locus for Alzheimer's disease on chromosome 10

Science 2000; 290(5500):2304-2305.

Blacker D, Crystal AS, Wilcox MA, Laird NM, Tanzi RE

In reply - alpha-2 macroglobulin gene and Alzheimer disease

Nature Genetics 1999; 22:21-22.

Grubber JM, Saunders AM, Crane-Gatherum AR, Scott WK, Martin ER, Haynes CS, Conneally PM, Small GW, Roses AD, Haines JL, Pericak-Vance MA

Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K)

Neurosci Lett 1999; 262(2):115-119.

Kehoe P, Wavrant-De Vrieze F, Crook R, Wu WS, Holmans P, Fenton I, Spurlock G, Norton N, Williams H, Williams N

A full genome scan for late onset Alzheimer's disease

Human molecular genetics 1999; 8(2):237-245.

Rogaeva E, Premkumar S, Grubber J, Serneels L, Scott W, Kawarai T, Song Y, Hill DLM, Abou-Donia SM, Martin ER, Vance JJ, Yu G, Orlacchio A, Pei Y, Nishimura M, Supala A, Roberge B, Saunders AM, Roses AD, Schmechel D, Crane-Gatherum A, Sorbi S, Bruni A, Small GW, Conneally PM, Haines JL, Van Leuven F, St George-Hyslop P, Farrer LA, Pericak-Vance MA

An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease

Nature Genet 1999; 22:19-21.

Rudrasingham V, Wavrant-DeVrieze F, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Rice F, Perez-Tur J, Frigard S, Chartier-Harlin M-C, Goate A, Hardy J, Own M, Williams J

Linkage but not association between alph-2-macroglobulin and late onset Alzheimer's disease

Nature Genet 1999; 22:17-19.

Wavrant-DeVrieze F, Crook R, Holmans P, Kehoe P, Owen MJ, Williams J, Roehl K, Laliiri D, Shears S, Booth J, Wu W, Goate A, Chartier-Harlin M-C, Hardy J, Perez-Tur J

Genetics variability at the APP locus may contribute to late-onset Alzheimer's disease

Neurosci Lett 1999; 269:67-70.

Wavrant-DeVrièze F, Rudrasingham V, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Holmans P, Rice F

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease

Neuroscience letters 1999; 262(2):137-139.

Blacker D, Wilcox MA, Laird NM, Rodes L, Horvath SM, Go RCP, Perry R, Watson B, Bassett SS, McInnis MG

Alpha-2 macroglobulin is genetically associated with Alzheimer disease

Nature genetics 1998; 19(4):357-360.

Wu WS, Holmans P, Wavrant-DeVrièze F, Shears S, Kehoe P, Crook R, Booth J, Williams N, Pérez-Tur J, Roehl K

Genetic studies on chromosome 12 in late-onset Alzheimer disease

Jama 1998; 280(7):619-622.

Blacker D, Haines JL, Rodes L, Terwedow H, Go RCP, Harrell LE, Perry RT, Bassett SS, Chase G, Meyers D, Albert MS, Tanzi R

APOE-4 and age-at-onset of Alzheimer's disease: the NIMH Genetics Initiative

Neurology 1997; 48(1):139-147.

Farrer AL, Cupples LA, Haines JL, Hyman B, Kulull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van Dujin CM, for the APOE and Alzheimer Disease Meta Analysis Consortium

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease

JAMA 1997; 278(16):1349-1356.

Blacker D, Albert MS, Bassett SS, Go, RCP, Harrell LE, Folstein MF

Reliability and validity of NINCDS-ADRDA criteria for Alzheimer's disease

Arch Neurol 1994; 51(12):1198-1204.

LIDDELL MB, MATHUR M, OWEN MJ

ADOLFSSON R, DRUGGE U, NYLANDER PO 57 AND HOLMGREN G

Psychiatric Genetics 1993; 3:157.

Anorexia Nervosa

Liu X, Kelsoe JR, Greenwood TA

A Genome-wide Association Study of Bipolar Disorder with Comorbid Eating Disorder Replicates the SOX2-OT Region

Journal of affective disorders 2015; 189:141-149.

Saunders EF, Fitzgerald KD, Zhang P, McInnis MG

CLINICAL FEATURES OF BIPOLAR DISORDER COMORBID WITH ANXIETY DISORDERS DIFFER BETWEEN MEN AND WOMEN

Depression and anxiety 2012; 29(8):739-746.

Kaye Walter H, Bulik Cynthia M, Plotnicov Katherine, Thornton Laura, Devlin Bernie, Fichter Manfred M, Treasure Janet, Kaplan Allan, Woodside D Blake, Johnson Craig L, Halmi Katherine, Brandt Harry A, Crawford Steve, Mitchell James E, Strober Michael, Berrettini Wade, Jones Ian

The genetics of anorexia nervosa collaborative study: methods and sample description.

The International journal of eating disorders 2008; 41(4):289-300.

Nemeroff CB

Comorbidity of mood and anxiety disorders: the rule, not the exception?

American Journal of Psychiatry 2002

Autism

Connacher R, Williams M, Prem S, Yeung PL, Matteson P, Mehta M, Markov A, Peng C, Zhou X, McDermott CR, Pang ZP, Flax J, Brzustowicz L, Lu CW, Millonig JH, DiCicco-Bloom E

Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses

Stem Cell Reports 2022; 17(6):1380-1394.

Hernandez LM, Lawrence KE, Padgaonkar NT, Inada M, Hoekstra JN, Lowe JK, Eilbott J, Jack A, Aylward E, Gaab N, Van Horn JD, Bernier RA, McPartland JC, Webb SJ, Pelphrey KA, Green SA, Geschwind DH, Bookheimer SY, Dapretto M

Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity

Translational Psychiatry 2020; 10:82.

McPartland JC, Bernier RA, Jeste SS, Dawson G, Nelson CA, Chawarska K, Earl R, Faja S, Johnson SP, Sikich L, Brandt CA, Dziura JD, Rozenblit L, Hellemann G, Levin AR, Murias M, Naples AJ, Platt ML, Sabatos-DeVito M, Shic F, Senturk D, Sugar CA, Webb SJ

The Autism Biomarkers Consortium for Clinical Trials (ABC-CT): Scientific Context, Study Design, and Progress Toward Biomarker Qualification

Frontiers in Integrative Neuroscience 2020; 14:16.

Patowary Ashok, Won So Yeon, Oh Shin Ji, Nesbitt Ryan R, Archer Marilyn, Nickerson Debbie, Raskind Wendy H, Bernier Raphael, Lee Ji Eun, Brkanac Zoran

Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.

Translational psychiatry 2019; 9(1):4.

Ruzzo EK, Pérez-Cano L, Jung JY, Wang LK, Kashef-Haghighi D, Hartl C, Singh C, Xu J, Hoekstra JN, Leventhal O, Leppa VM, Gandal MJ, Paskov K, Stockham N, Polioudakis D, Lowe JK, Prober DA, Geschwind DH, Wall DP

Inherited and de novo genetic risk for autism impacts shared networks

Cell 2019; 178(4):850-866.e26.

Rubinstein M, Patowary A, Stanaway I B, McCord E, Nesbitt R R, Archer M, Scheuer T, Nickerson D, Raskind W H, Wijsman E M, Bernier R, Catterall W A, Brkanac Z

null

Molecular psychiatry 2018; 23(2):231-239.

Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, Dea J, Duhn C, Erdman CA, Gilson MC, Yadav R, Handsaker RE, Kashin S, Klei L, Mandell JD, Nowakowski TJ, Liu Y, Pochareddy S, Smith L, Walker MF, Waterman MJ, He X, Kriegstein AR, Rubenstein JL, Sestan N, McCarroll SA, Neale BM, Coon H, Willsey AJ, Buxbaum JD, Daly MJ, State MW, Quinlan AR, Marth GT, Roeder K, Devlin B, Talkowski ME, Sanders SJ

An analytical framework for whole genome sequence association studies and its implications for autism spectrum disorder

Nature genetics 2018; 50(5):727-736.

Boland Michael J, Nazor Kristopher L, Tran Ha T, Szücs Attila, Lynch Candace L, Paredes Ryder, Tassone Flora, Sanna Pietro Paolo, Hagerman Randi J, Loring Jeanne F

Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome.

Brain : a journal of neurology 2017; 140(3):582-598.

Bruni Matthew, Flax Judy F, Buyske Steven, Shindhelm Amber D, Witton Caroline, Brzustowicz Linda M, Bartlett Christopher W

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds.

Behavior genetics 2017; 47(2):193-201.

Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism

Molecular Autism 2017; 8:14.

Geisheker Madeleine R, Heymann Gabriel, Wang Tianyun, Coe Bradley P, Turner Tychele N, Stessman Holly A F, Hoekzema Kendra, Kvarnung Malin, Shaw Marie, Friend Kathryn, Liebelt Jan, Barnett Christopher, Thompson Elizabeth M, Haan Eric, Guo Hui, Anderlid Britt-Marie, Nordgren Ann, Lindstrand Anna, Vandeweyer Geert, Alberti Antonino, Avola Emanuela, Vinci Mirella, Giusto Stefania, Pramparo Tiziano, Pierce Karen, Nalabolu Srinivasa, Michaelson Jacob J, Sedlacek Zdenek, Santen Gijs W E, Peeters Hilde, Hakonarson Hakon, Courchesne Eric, Romano Corrado, Kooy R Frank, Bernier Raphael A, Nordenskjöld Magnus, Gecz Jozef, Xia Kun, Zweifel Larry S, Eichler Evan E

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Nature neuroscience 2017; 20(8):1043-1051.

Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PM, Li Q, Hakonarson H

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genome Medicine 2017; 9:106.

Patowary Ashok, Nesbitt Ryan, Archer Marilyn, Bernier Raphael, Brkanac Zoran

Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.

Autism research : official journal of the International Society for Autism Research 2017; 10(8):1338-1343.

Begum F, Chowdhury R, Cheung VG, Sherman SL, Feingold E

Genome-Wide Association Study of Meiotic Recombination Phenotypes

G3: Genes|Genomes|Genetics 2016; 6(12):3995-4007.

Cáceres A, Esko T, Pappa I, Gutiérrez A, Lopez-Espinosa MJ, Llop S, Bustamante M, Tiemeier H, Metspalu A, Joshi PK, Wilsonx JF, Reina-Castillón J, Shin J, Pausova Z, Paus T, Sunyer J, Pérez-Jurado LA, González JR

Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence

PLoS ONE 2016; 11(6):e0157739.

Darbro BW, Singh R, Zimmerman MB, Mahajan VB, Bassuk AG

Autism Linked to Increased Oncogene Mutations but Decreased Cancer Rate

PLoS ONE 2016; 11(3):e0149041.

Doan RN, Bae BI, Cubelos B, Chang C, Hossain AA, Al-Saad S, Mukaddes NM, Oner O, Al-Saffar M, Balkhy S, Gascon GG, Nieto M, Walsh CA

Mutations in Human Accelerated Regions (HARs) Disrupt Cognition and Social Behavior

Cell 2016; 167(2):341-354.e12.

Leppa Virpi M, Kravitz Stephanie N, Martin Christa Lese, Andrieux Joris, Le Caignec Cedric, Martin-Coignard Dominique, DyBuncio Christina, Sanders Stephan J, Lowe Jennifer K, Cantor Rita M, Geschwind Daniel H

Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.

American journal of human genetics 2016; 99(3):540-554.

Martin PM, Stanley RE, Ross AP, Freitas AE, Moyer CE, Brumback AC, Iafrati J, Stapornwongkul KS, Dominguez S, Kivimäe S, Mulligan KA, Pirooznia M, McCombie WR, Potash JB, Zandi PP, Purcell SM, Sanders SJ, Zuo Y, Sohal VS, Cheyette BN

DIXDC1 contributes to psychiatric susceptibility by regulating dendritic spine and glutamatergic synapse density via GSK3 and Wnt/β-catenin signaling

Molecular psychiatry 2016; 10.1038/mp.2016.184.

Otowa T, Hek K, Lee M, Byrne EM, Mirza SS, Nivard MG, Bigdeli T, Aggen SH, Adkins D, Wolen A, Fanous A, Keller MC, Castelao E, Kutalik Z, Van der Auwera S, Homuth G, Nauck M, Teumer A, Milaneschi Y, Hottenga JJ, Direk N, Hofman A, Uitterlinden A, Mulder CL, Henders AK, Medland SE, Gordon S, Heath AC, Madden PA, Pergadia M, van der Most PJ, Nolte IM, van Oort FV, Hartman CA, Oldehinkel AJ, Preisig M, Grabe HJ, Middeldorp CM, Penninx BW, Boomsma D, Martin NG, Montgomery G, Maher BS, van den Oord EJ, Wray NR, Tiemeier H, Hettema JM

Meta-analysis of genome-wide association studies of anxiety disorders

Molecular psychiatry 2016; 10.1038/mp.2015.197.

Rubinstein M, Patowary A, Stanaway IB, McCord E, Nesbitt RR, Archer M, Scheuer T, Nickerson D, Raskind WH, Wijsman EM, Bernier R, Catterall WA, Brkanac Z

Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism

Molecular Psychiatry 2016; 23(2):231-239.

Schaefer KA, Toral MA, Velez G, Cox AJ, Baker SA, Borcherding NC, Colgan DF, Bondada V, Mashburn CB, Yu CG, Geddes JW, Tsang SH, Bassuk AG, Mahajan VB

Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses

Investigative Ophthalmology & Visual Science 2016; 57(6):2509-2521.

Engchuan W, Dhindsa K, Lionel AC, Scherer SW, Chan JH, Merico D

Performance of case-control rare copy number variation annotation in classification of autism

BMC Medical Genomics 2015; 8(Suppl 1):S7.

Li J, Ma Z, Shi M, Malty RH, Aoki H, Minic Z, Phanse S, Jin K, Wall DP, Zhang Z, Urban AE, Hallmayer J, Babu M, Snyder M

Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders

Cell systems 2015; 1(5):361-374.

Lowe Jennifer K, Werling Donna M, Constantino John N, Cantor Rita M, Geschwind Daniel H

Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.

The American journal of psychiatry 2015; 172(3):266-75.

Siegel Matthew, Smith Kahsi A, Mazefsky Carla, Gabriels Robin L, Erickson Craig, Kaplan Desmond, Morrow Eric M, Wink Logan, Santangelo Susan L

The autism inpatient collection: methods and preliminary sample description.

Molecular autism 2015; 6:61.

Anney RJL, Nurnberger JI, Sutcliffe JS, Bolshakova N, Vieland V, Brownfeld JM, Hallmayer J, Geschwind D, Pinto D, Vicente AM

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

Bartlett Christopher W, Hou Liping, Flax Judy F, Hare Abby, Cheong Soo Yeon, Fermano Zena, Zimmerman-Bier Barbie, Cartwright Charles, Azaro Marco A, Buyske Steven, Brzustowicz Linda M

A genome scan for loci shared by autism spectrum disorder and language impairment.

The American journal of psychiatry 2014; 171(1):72-81.

Bowton E, Saunders C, Reddy IA, Campbell NG, Hamilton PJ, Henry LK, Coon H, Sakrikar D, Veenstra-VanderWeele JM, Blakely RD

SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking

Translational psychiatry 2014; 4(10):e464.

Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, Pinto D, Poustka F, Scherer SW, Shih A, Sutcliffe JS, Szatmari P, Vicente AM, Vieland V, Gallagher L

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

Mol Autism 2014; 5(1):34.

Davis Jonathan M, Searles Veronica B, Anderson Nathan, Keeney Jonathon, Dumas Laura, Sikela James M

DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism.

PLoS genetics 2014; 10(3):e1004241.

Gupta AR, Pirruccello M, Cheng F, Kang HJ, Fernandez TV, Baskin JM, Choi M, Liu L, Ercan-Sencicek AG, Murdoch JD

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders

Molecular autism 2014; 5(1):1-14.

Lowe JK, Werling DM, Constantino JN, Cantor RM, Geschwind DH

Quantitative linkage analysis to the autism endophenotype social responsiveness identifies genome-wide significant linkage to two regions on chromosome 8

The American journal of psychiatry 2014; 172(3):266-275.

Trubetskoy V, Rodriguez A, Dave U, Campbell N, Crawford EL, Cook EH, Sutcliffe JS, Foster I, Madduri R, Cox NJ, Davis LK

Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes

Bioinformatics 2014; 31(2):187-193.

Werling Donna M, Lowe Jennifer K, Luo Rui, Cantor Rita M, Geschwind Daniel H

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.

Molecular autism 2014; 5(1):13.

Wittkowski KM, Sonakya V, Bigio B, Tonn MK, Shic F, Ascano M, Nasca C, Gold-Von Simson G

A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism

Translational Psychiatry 2014; 4(1):e354-.

Bill BR, Lowe JK, Dybuncio CT, Fogel BL

Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder

Int Rev Neurobiol 2013; 113:251-267.

Campbell NG, Zhu CB, Lindler KM, Yaspan BL, Kistner-Griffin E, Hewlett WA, Tate CG, Blakely RD, Sutcliffe JS

Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome

Molecular autism 2013; 4(1):1.

Cheng Y, Quinn JF, Weiss LA

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk

Human Molecular Genetics 2013; 22(14):2960-2972.

Cross-Disorder Group of the Psychiatric Genomics Consortium, et al

Genetic relaltionship between five psychiatric disorders estimated from genome-wide SNPs

Nat Genet 2013; 45(9):984-994.

Girirajan S, Johnson RL, Tassone F, Balciuniene J, Katiyar N, Fox K, Baker C, Srikanth A, Yeoh KH, Khoo SJ, Nauth TB, Hansen R, Ritchie M, Hertz-Picciotto I, Eichler EE, Pessah IN, Selleck SB

Global increases in both common and rare copy number load associated with autism

Human Molecular Genetics 2013; 22(14):2870-2880.

HADJIXENOFONTOS A, SCHMIDT MA, WHITEHEAD PL, KONIDARI I, HEDGES DJ, WRIGHT HH, ABRAMSON RK, MENON R, WILLIAMS SM, CUCCARO ML, HAINES JL, GILBERT JR, PERICAK-VANCE MA, MARTIN ER, MCCAULEY JL

Evaluating mitochondrial DNA variation in autism spectrum disorders

Annals of human genetics 2013; 77(1):9-21.

He Xin, Sanders Stephan J, Liu Li, De Rubeis Silvia, Lim Elaine T, Sutcliffe James S, Schellenberg Gerard D, Gibbs Richard A, Daly Mark J, Buxbaum Joseph D, State Matthew W, Devlin Bernie, Roeder Kathryn

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.

PLoS genetics 2013; 9(8):e1003671.

Lee Y, Ghosh D, Zhang Y

Association testing to detect gene-gene interactions on sex chromosomes in trio data

Frontiers in Genetics 2013; 4:239.

Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, Valladares O, Gabriel SB, DePristo M, Altshuler DM, Purcell SM; NHLBI Exome Sequencing Project, State MW, Boerwinkle E, Buxbaum JD, Cook EH, Gibbs RA, Schellenberg GD, Sutcliffe JS, Devlin B, Roeder K, Daly MJ

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

Neuron 2013; 77(2):235-242.

Liu L, Sabo A, Neale BM, Nagaswamy U, Stevens C, Lim E, Bodea CA, Muzny D, Reid JG, Banks E

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

PLoS Genet 2013; 9(4):e1003443.

Matsunami Nori, Hadley Dexter, Hensel Charles H, Christensen G Bryce, Kim Cecilia, Frackelton Edward, Thomas Kelly, da Silva Renata Pellegrino, Stevens Jeff, Baird Lisa, Otterud Brith, Ho Karen, Varvil Tena, Leppert Tami, Lambert Christophe G, Leppert Mark, Hakonarson Hakon

Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.

PloS one 2013; 8(1):e52239.

Parikshak NN, Luo R, Zhang A, Won H, Lowe JK, Chandran V, Horvath S, Geschwind DH

Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism cells

Cell 2013; 155(5):1008-1021.

Sampath S, Bhat S, Gupta S, O'Connor A, West AB, Arking DE, Chakravarti A

Defining the contribution of CNTNAP2 to autism susceptibility

PloS one 2013; 8(10):e77906.

Stein JL, Parikshak NN, Geschwind DH

Rare inherited variation in autism: beginning to see the forest and a few trees

Neuron 2013; 77(2):209-211.

Tsang KM, Croen LA, Torres AR, Kharrazi M, Delorenze GN, Windham GC, Yoshida CK, Zerbo O, Weiss LA

A genome-wide survey of transgenerational genetic effects in autism

PLoS ONE 2013; 8(10):e76978.

Wang HZ, Qin HD, Guo W, Samuels J, Shugart YY

New insights into the genetic mechanism of IQ in autism spectrum disorders

Frontiers in Genetics 2013; 4:195.

Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW, Autism Sequencing Consortium

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders

Neuron 2012; 76(6):1052-1056.

Celestino-Soper PB, Violante S, Crawford EL, Luo R, Lionel AC, Delaby E, Cai G, Sadikovic B, Lee K, Lo C, Gao K, Person RE, Moss TJ, German JR, Huang N, Shinawi M, Treadwell-Deering D, Szatmari P, Roberts W, Fernandez B, Schroer RJ, Stevenson RE, Buxbaum JD, Betancur C, Scherer SW, Sanders SJ, Geschwind DH, Sutcliffe JS, Hurles ME, Wanders RJ, Shaw CA, Leal SM, Cook EH Jr, Goin-Kochel RP, Vaz FM, Beaudet AL

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Proc Natl Acad Sci USA 2012; 109(21):7974-7981.

Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin CL, Martin DM, Morrow EM, Walsh CA, Melhem NM, Chaste P, Sutcliffe JS, State MW, Cook EH Jr, Roeder K, Devlin B

Common genetic variants, acting additively, are a major source of risk for autism

Molecular Autism 2012; 3:9.

Konopka G, Wexler E, Rosen E, Mukamel Z, Osborn GE, Chen L, Lu D, Gao F, Gao K, Lowe JK, Geschwind DH

Modeling the functional genomics of autism using human neurons

Mol Psychiatry 2012; 17(2):202-214.

Michaelson JJ, Shi Y, Gujral M, Zheng H, Malhotra D, Jin X, Minghan J, Liu G, Greer D, Bhandari A, Wu W, Corominas R, Peoples Á, Koren A, Gore A, Kang S, Lin GN, Estabillo J, Gadomski T, Singh B, Zhang K, Akshoomoff N, Corsello C, McCarroll S, Iakoucheva LM, Li Y, Wang J, Sebat J

Whole Genome Sequencing in Autism Identifies Hotspots for De Novo Germline Mutation

Cell 2012; 151(7):1431-1442.

Mondal K, Ramachandran D, Patel VC, Hagen KR, Bose P, Cutler DJ, Zwick ME

Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder

Human Molecular Genetics 2012; 21(19):4356-4364.

Moreno-De-Luca D, Sanders SJ, Willsey AJ, Mulle JG, Lowe JK, Geschwind DH, State MW, Martin CL, Ledbetter D

Using large clinical datasets to infer pathogenicity for rare CNVs in autism spectrum disorders

Mol Psychiatry 2012; 18(10):1090-1095.

Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Shafer C, Liu H, Zhao T, Cai G, Lihm J, Dannenfelser R, Jabado O, Peralta Z, Nagaswamy U, Muzny D, Reid JG, Newsham I, Wu Y, Lewis L, Han Y, Voight BF, Lim E, Rossin E, Kirby A, Flannick J, Fromer M, Shakir K, Fennell T, Garimella K, Banks E, Poplin R, Gabriel S, DePristo M, Wimbish JR, Boone BE, Levy SE, Betancur C, Sunyaev S, Boerwinkle E, Buxbaum JD, Cook EH Jr, Devlin B, Gibbs RA, Roeder K, Schellenberg GD, Sutcliffe JS, Daly MJ

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature 2012; 485(7397):242-245.

O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

Nature 2012; 485(7397):246-250.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E, Hougaard DM, Ørntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Milovancevic MP, Tosevski DL, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K

Common Variant at 16p11.2 Conferring Risk of Psychosis

Molecular psychiatry 2012; 19(1):10.1038/mp.2012.157.

Steinberg KM, Ramachandran D, Patel VC, Shetty AC, Cutler DJ, Zwick ME

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

Molecular Autism 2012; 3:8.

Bowers Katherine, Li Qing, Bressler Joseph, Avramopoulos Dimitrios, Newschaffer Craig, Fallin M Daniele

Glutathione pathway gene variation and risk of autism spectrum disorders.

Journal of neurodevelopmental disorders 2011; 3(2):132-43.

Bowers K, Li Q, Bressler J, Avramopoulos D, Newschaffer C, Fallin MD

Glutathione pathway gene variation and risk of autism spectrum disorders

Journal of Neurodevelopmental Disorders 2011; 3(2):132-143.

Geschwind DH

Genetics of autism spectrum disorders

Trends Cogn Sci 2011; 15(9):409-416.

Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH

Parent-of-origin effects of the serotonin transporter gene associated with autism

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2011; 156(2):139-144.

Liu Y, Gibson J, Wheeler J, Kwee LC, Santiago-Turla CM, Akafo SK, Lichter PR, Gaasterland DE, Moroi SE, Challa P, Herndon LW, Girkin CA, Budenz DL, Richards JE, Allingham RR, Hauser MA

GALC Deletions Increase the Risk of Primary Open-Angle Glaucoma: The Role of Mendelian Variants in Complex Disease

PLoS ONE 2011; 6(11):e27134.

Mukamel Z, Konopka G, Wexler E, Osborn GE, Dong H, Bergman MY, Levitt P, Geschwind DH

Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk

J Neurosci 2011; 31(32):11437-11442.

Rudacille D

Distributed risk

Turner T, Pihur V, Chakravarti A

Quantifying and modeling birth order effects in autism

PloS one 2011; 6(10):.

Voineagu I, Wang X, Johnston P, Lowe JK, Tian Y, Horvath S, Mill J, Cantor RM, Blencowe BJ, Geschwind DH

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

Nature 2011; 474(7351):380-384.

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J

A genome-wide scan for common alleles affecting risk for autism

Hum Mol Genet 2010; 19(20):4072-4082.

Chakravarti A, Arking DE, Daly M, Carayol J, Rousseau F

Compositions and methods for diagnosing autism

Flax Judy F, Hare Abby, Azaro Marco A, Vieland Veronica J, Brzustowicz Linda M

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.

Journal of neurodevelopmental disorders 2010; 2(4):210-223.

Fradin D, Cheslack-Postava K, Ladd-Acosta C, Newschaffer C, Chakravarti A, Arking DE, Feinberg A, Fallin MD

Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs

PLoS ONE 2010; 5(9):e12513.

Hilton CL, Fitzgerald RT, Jackson KM, Maxim RA, Bosworth CC, Shattuck PT, Geschwind DH, Constantino JN

Brief report: Under-representation of African Americans in autism genetic research: a rationale for inclusion of subjects representing diverse family structures

J Autism Dev Disord 2010; 40(5):633-639.

Kumar Ravinesh A, Sudi Jyotsna, Babatz Timothy D, Brune Camille W, Oswald Donald, Yen Mayon, Nowak Norma J, Cook Edwin H, Christian Susan L, Dobyns William B

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

Journal of medical genetics 2010; 47(2):81-90.

Nijmeijer Judith S, Arias-Vásquez Alejandro, Rommelse Nanda N J, Altink Marieke E, Anney Richard J L, Asherson Philip, Banaschewski Tobias, Buschgens Cathelijne J M, Fliers Ellen A, Gill Michael, Minderaa Ruud B, Poustka Luise, Sergeant Joseph A, Buitelaar Jan K, Franke Barbara, Ebstein Richard P, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sonuga-Barke Edmund J S, Steinhausen Hans-Christoph, Faraone Stephen V, Hartman Catharina A, Hoekstra Pieter J

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.

Journal of the American Academy of Child and Adolescent Psychiatry 2010; 49(7):675-85.

Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, Piven J, Ponting CP, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Sequeira AF, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stein O, Sykes N, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Webber C, Weksberg R, Wing K, Wittemeyer K, Wood S, Wu J, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Devlin B, Ennis S, Gallagher L, Geschwind DH, Gill M, Haines JL, Hallmayer J, Miller J, Monaco AP, Nurnberger JI Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Scherer SW, Sutcliffe JS, Betancur C

Functional impact of global rare copy number variation in autism spectrum disorders

Nature 2010; 466(7304):368-372.

Soctt-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

Sci Transl Med 2010; 2(56):56ra80.

Strom SP, Stone JL, Ten Bosch JR, Merriman B, Cantor RM, Geschwind DH, Nelson SF

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene

Mol Psychiatry 2010; 15(10):996-1005.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL

Copy number and sequence variants implicate APBA2 as an autism candidate gene

Autism Research 2009; 2(6):359-364.

Benayed Rym, Choi Jiyeon, Matteson Paul G, Gharani Neda, Kamdar Silky, Brzustowicz Linda M, Millonig James H

Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.

Biological psychiatry 2009; 66(10):911-7.

Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH

Autism Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2

Biological psychiatry 2009; 66(10):911-917.

Bill BR, Geschwind DH

Genetic advances in autism: heteorgeneity and convergence on shared pathways

Curr Opin Genet Dev 2009; 19(3):271-278.

Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, Kustanovich V, Lajonchere CM, Singleton A, Kim J, Wassink TH, McMahon WM, Owley T, Sweeney JA, Coon H, Nurnberger JI, Li M, Cantor RM, Minshew NJ, Sutcliffe JS, Cook EH, Dawson G, Buxbaum JD, Grant SF, Schellenberg GD, Geschwind DH, Hakonarson H

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

PLoS Genet 2009; 5(6):e1000536.

Geschwind DH

Advances in autism

Annu Rev Med 2009; 60:367-380.

Geschwind DH, Konopka G

Neuroscience in the era of functional genomics and systems biology

Nature 2009; 461(7266):908-915.

Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, KaraMohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL

Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

PLoS ONE 2009; 4(2):e4582.

Prasad HC, Steiner JA, Sutcliffe JS, Blakely RD

Enhanced activity of human serotonin transporter variants associated with autism

Philosophical Transactions of the Royal Society B: Biological Sciences 2009; 364(1514):163-173.

Psychiatric GWAS Consortium Coordinating Committee, Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF

Genomewide association studies: history, rationale, and prospects for psychiatric disorders

Am J Psychiatry 2009; 166(5):540-556.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Nature 2009; 459(7246):528-533.

Weiss LA, Arking DE

A GENOME-WIDE LINKAGE AND ASSOCIATION SCAN REVEALS NOVEL LOCI FOR AUTISM

Nature 2009; 461(7265):802-808.

Abrahams BS, Geschwind DH

Advances in autism genetics: on the threshold of a new neurobiology

Nat Rev Genet 2008; 9(5):341-355.

Abu-Elneel K, Liu T, Gazzaniga FS, Nishimura Y, Wall DP, Geschwind DH, Lao K, Kosik KS

Heterogeneous dysregulation of microRNAs across the autism spectrum

Neurogenetics 2008; 9(3):153-161.

Alarcon M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Am J Hum Genet 2008; 82(1):150-159.

Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH

Association of common variants in the Joubert syndrome gene (AHI1) with autism

Hum Mol Genet 2008; 17(24):3887-3896.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

The American Journal of Human Genetics 2008; 82(1):160-164.

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW

Molecular cytogenetic analysis and resequencing of contactin associated portein-like 2 in autism spectrum disorders

Am J Hum Genet 2008; 82(1):165-173.

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

Autism Res 2008; 1(3):159-168.

Geschwind DH

Autism: many genes, common pathways

Cell 2008; 135(3):391-395.

Geschwind DH

Autism: Family connections

Nature 2008; 454(7206):838-839.

Kumar RA, Karamohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH Jr, Dobyns WB, Christian SL

Recurrent 16p11.2 microdeletions in autism

Human molecular genetics 2008; 17(4):628-638.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind DH, Bolton P, Craig IW

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

Genes Brain Behav 2008; 7(7):754-760.

Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ; Autism Consortium

Association between microdeletion and microduplication at 16p11.2 and autism

N Engl J Med 2008; 358(7):667-675.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14

Mol Psychiatry 2007; 12:376-384.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M

Strong association of de novo copy number mutations with autism

Science 2007; 316:445-449.

The Austism Genome Project Consortium; Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Roge B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bolte S, Feineis-Matthews S, Herbrecht E, Schmotzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemmer C, Koop F, Langemeijer M, Hijimans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchison A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Nat Genet 2007; 39(3):319-328.

Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA

An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder

Ann Hum Genet 2006; 70(Pt 3):281-292.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P

A genetic variant that disrupts MET transcription is associated with autism

Proc Natl Acad Sci USA 2006; 103(45):16834-16839.

Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

Neurogenetics 2006; 7(3):167-174.

Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcón M

Stratification Based on Language-Related Endophenotypes in Autism: Attempt to Replicate Reported Linkage

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006; 0(6):591-598.

Spence Sarah J, Cantor Rita M, Chung Lien, Kim Sharon, Geschwind Daniel H, Alarcón Maricela

Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006; 141B(6):591-8.

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook Jr EH, Ober C, Sutcliffe JS

Variation in ITGB3 is associated with whole blood serotonin level and autism susceptibility

Eur J Hum Genet 2006; 14:923-931.

Alarcon M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs

Mol Psychiatry 2005; 10:747-757.

Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines

Int J Dev Neurosci 2005; 23(2-3):221-234.

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

The American Journal of Human Genetics 2005; 77(5):851-868.

Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcon M, Nelson SF, Geschwind DH

Replication of autism linkage: fine-mapping peak at 17q21

Am J Hum Genet 2005; 76(6):1050-1056.

Hamilton SP, Woo JM, Carlson EJ, Ghanem N, Ekker M, Rubenstein JLR

Analysis of four DLX homeobox genes in autistic probands

BMC Genet 2005; 6:52.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

Am J Hum Genet 2005; 77(3):377-388.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

BMC Med Genet 2005; 6(1):1-11.

Sahoo T, Shaw CA, Young AS, Whitehouse NL, Schroer RJ, Stevenson RE, Beaudet AL

Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements

Am J Med Genet A 2005; 139A:106-113.

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, Delong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA

Analysis of the RELN gene as a genetic risk factor for autism

Mol Psychiatry 2005; 10:563-571.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

The American Journal of Human Genetics 2005; 77(2):265-279.

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

Mol Psychiatry 2004; 9(5):474-484.

Jiang YH, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

Am J Med Genet A 2004; 131(1):1-10.

McCauley JL, Olson LM, Amin T, Organ EL, Folstein SE, Haines JL, Sutcliffe JS

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism

Am J Med Genet 2004; 131B:51-59.

McCauley JL, Dowd M, Olson LM, Amin T, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

Am J Med Genet 2004; 127B:104-112.

Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA

Analysis of the austim chromosome 2 linkage region: GAD1 and other candidate genes

Neurosci Lett 2004; 372(3):209-214.

Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA

No association between the APOE gene and autism

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 125(1):57-60.

Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF

Evidence for sex-specific risk alleles in autism spectrum disorder

Am J Med Genet 2004; 131A(1):11-17.

Yonan AL, Alarcón M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Hank Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC

A Genomewide Screen of 345 Families for Autism-Susceptibility Loci

American Journal of Human Genetics 2003; 73(4):886-897.

Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC

Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction

Genes Brain Behav 2003; 2(5):303-320.

Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH, Autism Genetic Research Exchange Consortium

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

Am J Hum Genet 2002; 70(1):60-71.

Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iverson P, Hoh J, Ott J, Gilliam TC, Autism Genetic Resource Exchange Consortium

A genomewide screen for autism susceptibility loci

Am J Hum Genet 2001; 69(2):327-340.

Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorp D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kramer HC, Myers RM

A genomic screen of autism: Evidence for a multi-locus etiology

Am J Hum Genet 1999; 65:493-507.

Bipolar Disorder

Hesam-Shariati S, Overs BJ, Roberts G, Toma C, Watkeys OJ, Green MJ, Pierce KD, Edenberg HJ, Wilcox HC, Stapp EK, McInnis MG, Hulvershorn LA, Nurnberger JI, Schofield PR, Mitchell PB, Fullerton JM

Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder

Translational Psychiatry 2022; 12:310.

Hindley G, Bahrami S, Steen NE, O'Connell KS, Frei O, Shadrin A, Bettella F, Rødevand L, Fan CC, Dale AM, Djurovic S, Smeland OB, Andreassen OA

Characterising the shared genetic determinants of bipolar disorder, schizophrenia and risk-taking

Translational Psychiatry 2021; 11:466.

Hu B, Won H, Mah W, Park RB, Kassim B, Spiess K, Kozlenkov A, Crowley CA, Pochareddy S, Li Y, Dracheva S, Sestan N, Akbarian S, Geschwind DH

Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

Nature Communications 2021; 12:3968.

Coleman JR, Gaspar HA, Bryois J, Breen G

The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

Biological psychiatry 2019; 88(2):169-184.

Jons WA, Colby CL, McElroy SL, Frye MA, Biernacka JM, Winham SJ

Statistical methods for testing X chromosome variant associations: application to sex-specific characteristics of bipolar disorder

Biology of Sex Differences 2019; 10:57.

Mullins N, Bigdeli TB, Børglum AD, Coleman JR, Demontis D, Fanous AH, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A, Corvin A, Sanders AR, Forstner AJ, Reif A, Koller AC, Świątkowska B, Baune BT, Müller-Myhsok B, Konte B, Penninx BW, Pato C, Zai C, Rujescu D, Hougaard DM, Quested D, Levinson DF, Binder EB, Byrne EM, Agerbo E, Streit F, Mayoral F, Bellivier F, Degenhardt F, Breen G, Morken G, Turecki G, Rouleau GA, Grabe HJ, Völzke H, Jones I, Giegling I, Agartz I, Melle I, Lawrence J, Potash JB, Walters JT, Strohmaier J, Shi J, Hauser J, Biernacka JM, Vincent JB, Kelsoe J, Strauss JS, Lissowska J, Pimm J, Smoller JW, Guzman Parra J, Berger K, Scott LJ, Jones LA, Azevedo MH, Trzaskowski M, Kogevinas M, Rietschel M, Boks M, Ising M, Grigoroiu-Serbanescu M, Hamshere ML, Leboyer M, Frye M, Nöthen MM, Alda M, Preisig M, Nordentoft M, Boehnke M, O'Donovan MC, Owen MJ, Pato MT, Renteria M, Budde M, Weissman MM, Wray NR, Bass N, Craddock N, Smeland OB, Andreassen OA, Mors O, Gejman PV, Sklar P, McGrath P, Hoffmann P, McGuffin P, Lee PH, Mortensen PB, Kahn RS, Ophoff RA, Adolfsson R, Van der Auwera S, Djurovic S, Shyn SI, Kloiber S, Heilmann-Heimbach S, Jamain S, Hamilton SP, McElroy SL, Lucae S, Cichon S, Schulze TG, Hansen T, Werge T, Air TM, Nimgaonkar V, Appadurai V, Cahn W, Milaneschi Y, Kendler KS, McQuillin A, Lewis CM

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

The American journal of psychiatry 2019; 176(8):651-660.

Ho KW, Han S, Nielsen JV, Jancic D, Hing B, Fiedorowicz J, Weissman MM, Levinson DF, Potash JB

Genome-wide association study of seasonal affective disorder

Translational Psychiatry 2018; 8:190.

Maier RM, Zhu Z, Lee SH, Trzaskowski M, Ruderfer DM, Stahl EA, Ripke S, Wray NR, Yang J, Visscher PM, Robinson MR

Improving genetic prediction by leveraging genetic correlations among human diseases and traits

Nature Communications 2018; 9:989.

McElroy SL, Winham SJ, Cuellar-Barboza AB, Colby CL, Ho AM, Sicotte H, Larrabee BR, Crow S, Frye MA, Biernacka JM

Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8

Translational Psychiatry 2018; 8:40.

Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PM, Li Q, Hakonarson H

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genome Medicine 2017; 9:106.

Monson ET, Pirooznia M, Parla J, Kramer M, Goes FS, Gaine ME, Gaynor SC, de Klerk K, Jancic D, Karchin R, McCombie WR, Zandi PP, Potash JB, Willour VL

Assessment of Whole-Exome Sequence Data in Attempted Suicide within a Bipolar Disorder Cohort

Molecular Neuropsychiatry 2017; 3(1):1-11.

Pinsonneault JK, Frater JT, Kompa B, Mascarenhas R, Wang D, Sadee W

Intronic SNP in ESR1 encoding human estrogen receptor alpha is associated with brain ESR1 mRNA isoform expression and behavioral traits

PLoS ONE 2017; 12(6):e0179020.

Wilcox HC, Fullerton JM, Glowinski AL, Benke K, Kamali M, Hulvershorn LA, Stapp EK, Edenberg HJ, Roberts GM, Ghaziuddin N, Fisher C, Brucksch C, Frankland A, Toma C, Shaw AD, Kastelic E, Miller L, McInnis MG, Mitchell PB, Nurnberger JI Jr

Traumatic Stress Interacts With Bipolar Disorder Genetic Risk to Increase Risk for Suicide Attempts

Journal of the American Academy of Child and Adolescent Psychiatry 2017; 56(12):1073-1080.

Acikel C, Aydin Son Y, Celik C, Gul H

Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data

Neuropsychiatric Disease and Treatment 2016; 12:2997-3004.

Breen ME, Gaynor SC, Monson ET, de Klerk K, Parsons MG, Braun TA, DeLuca AP, Zandi PP, Potash JB, Willour VL

Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder

PLoS ONE 2016; 11(12):e0169158.

Coryell W, Kriener A, Butcher B, Nurnberger J, McMahon F, Berrettini W, Fiedorowicz J

Risk factors for suicide in bipolar I disorder in two prospectively studied cohorts

Journal of affective disorders 2016; 190:1-5.

Gonzalez S, Gupta J, Villa E, Mallawaarachchi I, Rodriguez M, Ramirez M, Zavala J, Armas R, Dassori A, Contreras J, Flores D, Jerez A, Ontiveros A, Nicolini H, Escamilla M

Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort

Bipolar Disorders 2016; 18(6):520-527.

Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, Baune BT, Bellivier F, Benabarre A, Bengesser S, Berrettini WH, Bhattacharjee AK, Biernacka JM, Birner A, Bloss CS, Brichant-Petitjean C, Bui ET, Byerley W, Cervantes P, Chillotti C, Cichon S, Colom F, Coryell W, Craig DW, Cruceanu C, Czerski PM, Davis T, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Edenberg HJ, Étain B, Falkai P, Foroud T, Forstner AJ, Frisén L, Frye MA, Fullerton JM, Gard S, Garnham JS, Gershon ES, Goes FS, Greenwood TA, Grigoroiu-Serbanescu M, Hauser J, Heilbronner U, Heilmann-Heimbach S, Herms S, Hipolito M, Hitturlingappa S, Hoffmann P, Hofmann A, Jamain S, Jiménez E, Kahn JP, Kassem L, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Koller DL, König B, Lackner N, Laje G, Lang M, Lavebratt C, Lawson WB, Leboyer M, Leckband SG, Liu C, Maaser A, Mahon PB, Maier W, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McInnis MG, McKinney R, Mitchell PB, Mitjans M, Mondimore FM, Monteleone P, Mühleisen TW, Nievergelt CM, Nöthen MM, Novák T, Nurnberger JI Jr, Nwulia EA, Ösby U, Pfennig A, Potash JB, Propping P, Reif A, Reininghaus E, Rice J, Rietschel M, Rouleau GA, Rybakowski JK, Schalling M, Scheftner WA, Schofield PR, Schork NJ, Schulze TG, Schumacher J, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Smith EN, Squassina A, Stamm T, Stopkova P, Streit F, Strohmaier J, Szelinger S, Tighe SK, Tortorella A, Turecki G, Vieta E, Volkert J, Witt SH, Wright A, Zandi PP, Zhang P, Zollner S, McMahon FJ

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Human Molecular Genetics 2016; 25(15):3383-3394.

Hou L, Heilbronner U, Degenhardt F, Adli M, Akiyama K, Akula N, Ardau R, Arias B, Backlund L, Banzato CE, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A, Brichant-Petitjean C, Bui ET, Cervantes P, Chen GB, Chen HC, Chillotti C, Cichon S, Clark SR, Colom F, Cousins D, Cruceanu C, Czerski PM, Dantas CR, Dayer A, Étain B, Falkai P, Forstner AJ, Frisén L, Fullerton JM, Gard S, Garnham JS, Goes FS, Grof P, Gruber O, Hashimoto R, Hauser J, Herms S, Hoffmann P, Hofmann A, Jamain S, Jiménez E, Kahn JP, Kassem L, Kittel-Schneider S, Kliwicki S, König B, Kusumi I, Lackner N, Laje G, Landén M, Lavebratt C, Leboyer M, Leckband SG, López Jaramillo CA, MacQueen G, Manchia M, Martinsson L, Mattheisen M, McCarthy MJ, McElroy S, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, Nöthen MM, Ösby U, Ozaki N, Perlis RH, Pfennig A, Reich-Erkelenz D, Rouleau GA, Schofield PR, Schubert KO, Schweizer BW, Seemüller F, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Smoller JW, Squassina A, Stamm T, Stopkova P, Tighe SK, Tortorella A, Turecki G, Volkert J, Witt S, Wright A, Young LT, Zandi PP, Potash JB, DePaulo JR, Bauer M, Reininghaus E, Novák T, Aubry JM, Maj M, Baune BT, Mitchell PB, Vieta E, Frye MA, Rybakowski JK, Kuo PH, Kato T, Grigoroiu-Serbanescu M, Reif A, Zompo MD, Bellivier F, Schalling M, Wray NR, Kelsoe J, Alda M, Rietschel M, McMahon FJ, Schulze TG

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

Lancet (London, England) 2016; 387(10023):1085-1093.

Martin PM, Stanley RE, Ross AP, Freitas AE, Moyer CE, Brumback AC, Iafrati J, Stapornwongkul KS, Dominguez S, Kivimäe S, Mulligan KA, Pirooznia M, McCombie WR, Potash JB, Zandi PP, Purcell SM, Sanders SJ, Zuo Y, Sohal VS, Cheyette BN

DIXDC1 contributes to psychiatric susceptibility by regulating dendritic spine and glutamatergic synapse density via GSK3 and Wnt/β-catenin signaling

Molecular psychiatry 2016; 10.1038/mp.2016.184.

Monson ET, de Klerk K, Gaynor SC, Wagner AH, Breen ME, Parsons M, Casavant TL, Zandi PP, Potash JB, Willour VL

Whole-Gene Sequencing Investigation of SAT1 in Attempted Suicide

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016; 171(6):888-895.

Qiu F, Akiskal HS, Kelsoe JR, Greenwood TA

Factor Analysis of Temperament and Personality Traits in Bipolar Patients: Correlates with Comorbidity and Disorder Severity

Journal of affective disorders 2016; 207:282-290.

Rao AR, Yourshaw M, Christensen B, Nelson SF, Kerner B

Rare deleterious mutations are associated with disease in bipolar disorder families

Molecular psychiatry 2016; 10.1038/mp.2016.181.

Ross J, Gedvilaite E, Badner JA, Erdman C, Baird L, Matsunami N, Leppert M, Xing J, Byerley W

A Rare Variant in CACNA1D Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree

Molecular Neuropsychiatry 2016; 2(3):145-150.

Stange JP, Sylvia LG, da Silva Magalhães PV, Miklowitz DJ, Otto MW, Frank E, Yim C, Berk M, Dougherty DD, Nierenberg AA, Deckersbach T

Affective instability and the course of bipolar depression: results from the STEP-BD randomised controlled trial of psychosocial treatment

The British Journal of Psychiatry 2016; 208(4):352-358.

Acikel C, Son YA, Celik C, Tutuncu R

Evaluation of Whole Genome Association Study Data in Bipolar Disorders: Potential Novel SNPs and Genes

KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY 2015; 25(1):12-18.

Ament SA, Szelinger S, Glusman G, Ashworth J, Hou L, Akula N, Shekhtman T, Badner JA, Brunkow ME, Mauldin DE

Rare variants in neuronal excitability genes influence risk for bipolar disorder

Proceedings of the National Academy of Sciences 2015; 112(11):3576-3581.

Breen ME, Seifuddin F, Zandi PP, Potash JB, Willour VL

Investigating the role of early childhood abuse and HPA axis genes in suicide attempters with bipolar disorder

Psychiatric genetics 2015; 25(3):106-111.

Cho CH, Lee HJ, Woo HG, Choi JH, Greenwood TA, Kelsoe JR

CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis

Psychiatry Investigation 2015; 12(3):402-407.

Drago A, Crisafulli C, Calabrò M, Serretti A

Enrichment pathway analysis. The inflammatory genetic background in bipolar disorder

Journal of affective disorders 2015; 179:88-94.

Fabbri C, Serretti A

Genetics of long-term treatment outcome in bipolar disorder

Prog Neuropsychopharmacol Biol Psychiatry 2015; 65:17-24.

GRAAE LISETTE, PADDOCK SILVIA, BELIN ANDREACARMINE

ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide

Genetics research 2015; 97:e8.

Jacobsen KK, Nievergelt CM, Zayats T, Greenwood TA, Anttila V, Akiskal HS, Haavik J, Fasmer OB, Kelsoe JR, Johansson S

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

Journal of affective disorders 2015; 172:453-461.

Leonpacher AK, Liebers D, Pirooznia M, Jancic D, MacKinnon DF, Mondimore FM, Schweizer B, Potash JB, Zandi PP, Goes FS

Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features

Psychological medicine 2015; 1-10.

Leonpacher AK, Liebers D, Pirooznia M, Jancic D, MacKinnon DF, Mondimore FM, Schweizer B, Potash JB, Zandi PP, Goes FS

Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features

Psychological medicine 2015; 45(11):2437-2446.

Liu X, Kelsoe JR, Greenwood TA

A Genome-wide Association Study of Bipolar Disorder with Comorbid Eating Disorder Replicates the SOX2-OT Region

Journal of affective disorders 2015; 189:141-149.

Nurnberger JI, Wilcox HC, Liu H, Fullerton JM, Mitchell PB, Foroud T, McInnis MG, Edenberg HJ, Schofield PR, Glowinski AL

Assessment of First and Second Degree Relatives of Individuals With Bipolar Disorder Shows Increased Genetic Risk Scores in Both Affected Relatives and Young At-Risk Individuals

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2015; 168(7):617-629.

Perez-Andreu V, Roberts KG, Xu H, Smith C, Zhang H, Yang W, Harvey RC, Payne-Turner D, Devidas M, Cheng IM, Carroll WL, Heerema NA, Carroll AJ, Raetz EA, Gastier-Foster JM, Marcucci G, Bloomfield CD, Mrózek K, Kohlschmidt J, Stock W, Kornblau SM, Konopleva M, Paietta E, Rowe JM, Luger SM, Tallman MS, Dean M, Burchard EG, Torgerson DG, Yue F, Wang Y, Pui CH, Jeha S, Relling MV, Evans WE, Gerhard DS, Loh ML, Willman CL, Hunger SP, Mullighan CG, Yang JJ

A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults

Blood 2015; 125(4):680-686.

Swaminathan S, Koller DL, Foroud T, Edenberg HJ, Xuei X, Niculescu AB, Nurnberger JI, Bipolar Genome Study (BiGS) Consortium

Characteristics of Bipolar I patients grouped by externalizing disorders

Journal of affective disorders 2015; 178:206-214.

Yeh FC, Kao CF, Kuo PH

Explore the Features of Brain-Derived Neurotrophic Factor in Mood Disorders

PLoS ONE 2015; 10(6):e0128605.

Zhao Z, Xu J, Chen J, Kim S, Reimers M, Bacanu SA, Yu H, Liu C, Sun J, Wang Q

Transcriptome sequencing and genome-wide association analyses reveal lysosomal function and actin cytoskeleton remodeling in schizophrenia and bipolar disorder

Molecular psychiatry 2015; 20(5):563-572.

Boudebesse C, Geoffroy PA, Bellivier F, Henry C, Folkard S, Leboyer M, Etain B

Correlations between objective and subjective sleep and circadian markers in remitted patients with bipolar disorder

Chronobiology international 2014; 31(5):698-704.

Buchan JG, Alvarado DM, Haller G, Aferol H, Miller NH, Dobbs MB, Gurnett CA

Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis?

Clinical Orthopaedics and Related Research 2014; 472(10):3216-3225.

Castro VM, Minnier J, Murphy SN, Kohane I, Churchill SE, Gainer V, Cai T, Hoffnagle AG, Dai Y, Block S, Weill SR, Nadal-Vicens M, Pollastri AR, Rosenquist JN, Goryachev S, Ongur D, Sklar P, Perlis RH, Smoller JW for the International Cohort Collection for Bipolar Disorder

Validation of Electronic Health Record Phenotyping of Bipolar Disorder Cases and Controls

Am J Psychiatry 2014

Duan Jubao, Shi Jianxin, Fiorentino Alessia, Leites Catherine, Chen Xiangning, Moy Winton, Chen Jingchun, Alexandrov Boian S, Usheva Anny, He Deli, Freda Jessica, O'Brien Niamh L, McQuillin Andrew, Sanders Alan R, Gershon Elliot S, DeLisi Lynn E, Bishop Alan R, Gurling Hugh M D, Pato Michele T, Levinson Douglas F, Kendler Kenneth S, Pato Carlos N, Gejman Pablo V

A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder.

American journal of human genetics 2014; 95(6):744-53.

Duan J, Shi J, Fiorentino A, Leites C, Chen X, Moy W, Chen J, Alexandrov BS, Usheva A, He D, Freda J, O'Brien NL, McQuillin A, Sanders AR, Gershon ES, DeLisi LE, Bishop AR, Gurling HM, Pato MT, Levinson DF, Kendler KS, Pato CN, Gejman PV

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

American Journal of Human Genetics 2014; 95(6):744-753.

Faraone SV, Glatt SJ, Su J, Tsuang MT

Three potential susceptibility loci shown by a genome-wide scan for regions influencing the age at onset of mania

American Journal of Psychiatry 2014

Fiedorowicz JG, Jancic D, Potash JB, Butcher B, Coryell WH

Vascular mortality in participants of a bipolar genomics study

Psychosomatics 2014; 55(5):485-490.

Kimmel RJ, Kovacs I, Vrabel C, Wood B, Schalling M, Kelsoe JR

Cosegregation of bipolar disorder and autosomal-dominant medullary cystic kidney disease in a large family

American Journal of Psychiatry 2014

Lin PI, McInnis MG, Potash JB, Willour V, MacKinnon DF, DePaulo JR, Zandi PP

Clinical correlates and familial aggregation of age at onset in bipolar disorder

American Journal of Psychiatry 2014

MacKinnon DF, Zandi PP, Cooper J, Potash JB, Simpson SG, Gershon E, Nurnberger J, Reich T, DePaulo JR

Comorbid bipolar disorder and panic disorder in families with a high prevalence of bipolar disorder

American Journal of Psychiatry 2014

Nurnberger JI Jr, Koller DL, Jung J, Edenberg HJ, Foroud T, Guella I, Vawter MP, Kelsoe JR

Identification of Pathways for Bipolar Disorder A Meta-analysis

JAMA psychiatry 2014; 71(6):657-664.

Pirooznia M, Kramer M, Parla J, Goes FS, Potash JB, McCombie WR, Zandi PP

Validation and assessment of variant calling pipelines for next-generation sequencing

Human Genomics 2014; 8(1):14.

Schultze TG, Akula N, Breuer R, Steele J, Nalls MA, Singleton AB, Degenhardt FA, Nöthen MM, Cichon S, Rietschel M, Bipolar Genome Study, McMahon FJ

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder

World J Biol Psychiatry 2014; 15(3):200-208.

Winham SJ, Cuellar-Barboza AB, McElroy SL, Oliveros A, Crow S, Colby CL, Choi DS, Chauhan M, Frye MA, Biernacka JM

Bipolar disorder with comorbid binge eating history: A genome-wide association study implicates APOB

Journal of affective disorders 2014; 165:151-158.

Bigdeli TB, Maher BS, Zhao Z, Sun J, Medeiros H, Akula N, McMahon FJ, Carvalho C, Ferreira SR, Azevedo MH

Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 162(8):898-906.

Chang SH, Gao L, Li Z, Zhang WN, Du Y, Wang J

BDgene: a genetic database for bipolar disorder and its overlap with schizophrenia and major depressive disorder

Biological psychiatry 2013; 74(10):727-733.

Chen DT, Jiang X, Akula N, Shugart YY, Wendland JR, Steele CJ, Kassem L, Park JH, Chatterjee N, Jamain S, Cheng A, Leboyer M, Muglia P, Schultze TG, Cichon S, Nöthen MM, Rietschel M; BiGS, MaMahon FJ, Farmer A, McGuffin P, Craig I, Lewis C, Hosang G, Cohen-Woods S, Vincent JB, Kennedy JL, Strauss J

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

Mol Psychiatry 2013; 18(2):195-205.

Drago A, Giegling I, Schäfer M, Hartmann AM, Friedl M, Konte B, Möller HJ, De Ronchi D, Stassen HH, Serretti A

AKAP13, CACNA1, GRIK4 and GRIA1 genetic variations may be associated with haloperidol efficacy during acute treatment

Eur Neuropsychopharmacol 2013; 123(8):887-894.

Gonzalez S, Xu C, Ramirez M, Zavala J, Armas R, Contreras SA, Contreras J, Dassori A, Leach RJ, Flores D, Jerez A, Raventós H, Ontiveros A, Nicolini H, Escamilla M

Suggestive evidence for association between L-type voltage-gated calcium channel (CACNA1C) gene haplotypes and bipolar disorder in Latinos: a family-based association study

Bipolar disorders 2013; 15(2):206-214.

Greenwood TA, Joo EJ, Shektman T, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR

Association of Dopamine Transporter Gene Variants with Childhood ADHD Features in Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 0(2):137-145.

Greenwood TA, Badner JA, Byerley W, Keck PE, McElroy SL, Remick RA, Sadovnick AD, Akiskal HS, Kelsoe JR

Heritability and Genome-wide SNP Linkage Analysis of Temperament in Bipolar Disorder

Journal of affective disorders 2013; 150(3):1031-1040.

Greenwood TA, Badner JA, Byerley W, Keck PE, McElroy SL, Remick RA, Sadovnick AD, Kelsoe JR

Heritability and Linkage Analysis of Personality in Bipolar Disorder

Journal of affective disorders 2013; 151(2):748-755.

Jackson KJ, Fanous AH, Chen J, Kendler KS, Chen X

Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder

Psychiatric genetics 2013; 23(1):20-28.

Judy JT, Seifuddin F, Pirooznia M, Mahon PB, Jancic D, Goes FS, Schulze T, Cichon S, Noethen M, Rietschel M, DePaulo JR Jr, Potash JB, Zandi PP

Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder

Frontiers in Genetics 2013; 4:87.

Kemp DE, Sylvia LG, Calabrese JR, Nierenberg AA, Thase ME, Reilly-Harrington NA, Ostacher MJ, Leon AC, Ketter TA, Friedman ES, Bowden CL, Pencina M, Iosifescu DV

General Medical Burden in Bipolar Disorder: Findings from the LiTMUS Comparative Effectiveness Trial

Acta psychiatrica Scandinavica 2013; 129(1):10.1111/acps.12101.

Kerner B, Rao AR, Christensen B, Dandekar S, Yourshaw M, Nelson SF

Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways

Frontiers in Psychiatry 2013; 4:154.

Lee HJ, Woo HG, Greenwood TA, Kripke DF, Kelsoe JR

A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder

Journal of affective disorders 2013; 145(2):200-207.

Lencz T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L, Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nöthen MM, Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisanté A, Gregersen PK, Pe'er I, Malhotra AK, Goldman D, Darvasi A

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

Nature Communications 2013; 4:2739.

Pato MT, Sobell JL, Medeiros H, Abbott C, Skar B, Buckley PF, Bromet EJ, Escamilla MA, Fanous AH, Lehrer DS, Macciardi F, Malaspina D, McCarroll SA, Marder SR, Moran J, Morley CP, Nicolini H, Perkins DO, Purcell SM, Rapaport MH, Sklar P, Smoller JW, Knowles JA, Pato CN

The Genomic Psychiatry Cohort: Partners in Discovery

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 0(4):306-312.

Perez-Andreu V, Roberts KG, Harvey RC, Yang W, Cheng C, Pei D, Xu H, Gastier-Foster J, Shuyu E, Yew-Suang Lim J, Chen IM, Fan Y, Devidsa M, Borowitz MJ, Smith C, Neale G, Burchard EG, Torgerson DG, Klussmann FA, Villagran CR, Winick NJ, Camitta BM, Raetz E, Wood B, Yue F, Carroll WL, Larsen E, Bowman WP, Loh ML, Dean M, Bhojwani D, Pui CH, Evans WE, Relling MV, Hunger SP, Willman CL, Mullighan CG, Yang JJ

Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse

Nature genetics 2013; 45(12):1494-1498.

Rastelli CPB, Cheng Y, Weingarden J, Frank E, Swartz HA

Differences between unipolar depression and bipolar II depression in women

J Affect Disord 2013; 150(3):1120-1124.

Serretti A, Chiesa A, Calati R, Fabbri C, Sentissi O, De Ronchi D, Mendlewicz J, Souery D

Side effects associated with psychotropic medications in patients with bipolar disorder: evidence from two independent samples

Journal of psychopharmacology 2013; 0269881113485143.

Trotta A, Di Forti M, Mondelli V, Dazzan P, Pariante C, David A, Mulè A, Ferraro L, Formica I, Murray RM

Prevalence of bullying victimisation amongst first-episode psychosis patients and unaffected controls

Schizophrenia research 2013; 150(1):169-175.

Vijai J, Kirchhoff T, Schrader KA, Brown J, Dutra-Clarke AV, Manschreck C, Hansen N, Rau-Murthy R, Sarrel K, Przybylo J, Shah S, Cheguri S, Stadler Z, Zhang L, Paltiel O, Ben-Yehuda D, Viale A, Portlock C, Straus D, Lipkin SM, Lacher M, Robson M, Klein RJ, Zelenetz A, Offit K

Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies

PLoS Genetics 2013; 9(1):e1003220.

Alvarado DM, Buchan JG, Frick SL, Herzenberg JE, Dobbs MB, Gurnett CA

Copy number analysis of 413 isolated talipes equinovarus patients suggests role for transcriptional regulators of early limb development

European Journal of Human Genetics 2012; 21(4):373-380.

Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI Jr, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, Craddock N, Morris D, Segurado R, Gill M, Sadovnick D, Remick R, Keck P, Kelsoe J, Ayub M, MacLean A, Blackwood D, Liu CY, Gershon ES, McMahon W, Lyon G, Robinson R, Ross J, Byerley W

Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms

Molecular psychiatry 2012; 17(8):818-826.

Chen C, Cheng L, Grennan K, Pibiri F, Zhang C, Badner JA, Gershon ES, Liu C

Two Gene Co-expression Modules Differentiate Psychotics and Controls

Molecular psychiatry 2012; 18(12):1308-1314.

Doyle GA, Lai AT, Chou AD, Wang MJ, Gai X, Rappaport EF, Berrettini WH

Re-sequencing of ankyrin 3 exon 48 and case-control association analysis of rare variants in bipolar disorder type I

Bipolar disorders 2012; 14(8):809-821.

ETAIN B, LAJNEF M, BELLIVIER F, MATHIEU F, RAUST A, COCHET B, GARD S, M'BAILARA K, KAHN JP, ELGRABLI O

Clinical expression of bipolar disorder type I as a function of polarity and age at onset: convergent findings in samples from France and the USA

Journal of Clinical Psychiatry 2012; 73(4):e561-6.

Ferguson JP, Cho JH, Yang C, Zhao H

Empirical Bayes Correction for the Winner's Curse in Genetic Association Studies

Genetic epidemiology 2012; 37(1):60-68.

Goes FS, McCusker MG, Bienvenu OJ, MacKinnon DF, Mondimore FM, Schweizer B, DePaulo JR Jr, Potash JB

Co-morbid anxiety disorders in bipolar disorder and major depression : familial aggregation and clinical characteristics of co-morbid panic disorder, social phobia, specific phobia and obsessive-compulsive disorder

Psychological medicine 2012; 42(7):1449-1459.

Greenwood TA, Akiskal HS, Akiskal KK, Kelsoe JR

Genome-wide Association Study of Temperament in Bipolar Disorder Reveals Significant Associations To Three Novel Loci

Biological psychiatry 2012; 72(4):303-310.

Hammer C, Cichon S, Mühleisen TW, Haenisch B, Degenhardt F, Mattheisen M, Breuer R, Witt SH, Strohmaier J, Oruc L, Rivas F, Babadjanova G, Grigoroiu-Serbanescu M, Hauser J, Röth R, Rappold G, Rietschel M, Nöthen MM, Niesler B

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

Translational Psychiatry 2012; 2(4):e103-.

Jancic D, Seifuddin F, Zandi PP, Potash JB, Willour VL

Association study of X chromosome SNPs in attempted suicide

Psychiatry research 2012; 200(0):1044-1046.

Judy JT, Seifuddin F, Mahon PB, Huo Y, Goes FS, Jancic D, Schweizer B, Mondimore FM, MacKinnon DF, DePaulo JR Jr, Gershon ES, McMahon FJ, Cutler DJ, Zandi PP, Potash JB, Willour VL

Association Study of Serotonin Pathway Genes in Attempted Suicide

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2012; 0(1):112-119.

McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, Donald JA, Weickert CS, Mitchell PB, Schofield PR, Fullerton JM

Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26

PLoS ONE 2012; 7(5):e38172.

Polymorphisms SN

Europe PMC Funders Group

Mol Psychiatry 2012; 17(8):818-826.

Saunders EF, Fitzgerald KD, Zhang P, McInnis MG

CLINICAL FEATURES OF BIPOLAR DISORDER COMORBID WITH ANXIETY DISORDERS DIFFER BETWEEN MEN AND WOMEN

Depression and anxiety 2012; 29(8):739-746.

Sequeira A, Martin MV, Rollins B, Moon EA, Bunney WE, Macciardi F, Lupoli S, Smith EN, Kelsoe J, Magnan CN, van Oven M, Baldi P, Wallace DC, Vawter MP

Mitochondrial Mutations and Polymorphisms in Psychiatric Disorders

Frontiers in Genetics 2012; 3:103.

Sharma V, Pope CJ

Pregnancy and bipolar disorder: a systematic review

The Journal of clinical psychiatry 2012; 73(11):1,478-1455.

Song JY, Yu HY, Kim SH, Hwang SSH, Cho HS, Kim YS, Ha K, Ahn YM

Assessment of risk factors related to suicide attempts in patients with bipolar disorder

The Journal of nervous and mental disease 2012; 200(11):978-984.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E; GROUP, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B; Wellcome Trust Case Control Consortium S, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K

Common variant at 16p11 2 conferring risk of psychosis

Mol Psychiatry 2012; 19(1):108-114.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E, Hougaard DM, Ørntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Milovancevic MP, Tosevski DL, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K

Common Variant at 16p11.2 Conferring Risk of Psychosis

Molecular psychiatry 2012; 19(1):10.1038/mp.2012.157.

Swartz HA, Levenson JC, Frank E

Psychotherapy for bipolar II disorder: The role of interpersonal and social rhythm therapy

Prof Psychol Res Pr 2012; 43(2):145-153.

Yuan D, Zhu Z, Tan X, Liang J, Zeng C, Zhang J, Chen J, Ma L, Dogan A, Brockmann G

Methods for scoring the collective effect of SNPs: Minor alleles of common SNPs quantitatively affect traits/diseases and are under both positive and negative selection

arXiv preprint arXiv:1209.2911 2012

Agrawal A, Nurnberger JI Jr, Lynskey MT

Cannabis involvement in individuals with Bipolar Disorder

Psychiatry research 2011; 185(3):459-461.

Alliey-Rodriguez N, Zhang D, Badner JA, Lahey BB, Zhang X, Dinwiddie S, Romanos B, Plenys N, Liu C, Gershon ES

Genome-wide association study of personality traits in bipolar patients

Psychiatric genetics 2011; 21(4):190-194.

Byerley W, Badner JA

Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p

Psychiatric genetics 2011; 21(4):173-182.

Drago A, Crisafulli C, Serretti A

The genetics of antipsychotic induced tremors: A genome-wide pathway analysis on the STEP-BD SCP sample

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2011; 156(8):975-986.

Goes FS, Rongione M, Chen YC, Karchin R, Elhaik E, Potash JB

Exonic DNA Sequencing of ERBB4 in Bipolar Disorder

PLoS ONE 2011; 6(5):e20242.

Kerner B, Lambert CG, Muthén BO

Genome-wide association study in bipolar patients stratified by co-morbidity

PLoS One 2011; 6(12):e28477.

Machado-Vieira R, Pivovarova NB, Stanika RI, Yuan P, Wang Y, Zhou R, Zarate CA Jr, Drevets WC, Brantner CA, Baum A, Laje G, McMahon FJ, Chen G, Du J, Manji HK, Andrews SB

The Bcl-2 Gene Polymorphism rs956572AA Increases Inositol 1,4,5-Trisphosphate Receptor-Mediated Endoplasmic Reticulum Calcium Release in Subjects with Bipolar Disorder

Biological psychiatry 2011; 69(4):344-352.

Mahon PB, Pirooznia M, Goes FS, Seifuddin F, Steele J, Lee PH, Huang J, Hamshere M, DePaulo JR Jr, Kelsoe JR, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, Schulze T, McMahon FJ, Potash JB, Zandi PP

Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2011; 156B(3):370-378.

Mooney MA, Wilmot B, McWeeney SK

The GA and the GWAS: Using Genetic Algorithms to Search for Multi-locus Associations

IEEE/ACM transactions on computational biology and bioinformatics / IEEE, ACM 2011; 9(3):10.1109/TCBB.2011.145.

Nurnberger JI, McInnis M, Reich W, Kastelic E, Wilcox HC, Glowinski A, Mitchell P, Fisher C, Erpe M, Gershon ES

A high-risk study of bipolar disorder: childhood clinical phenotypes as precursors of major mood disorders

Archives of general psychiatry 2011; 68(10):1012-1020.

Piletz JE, Zhang X, Ranade R, Liu C

Database of Genetic Studies of Bipolar Disorder

Psychiatric genetics 2011; 21(2):57-68.

Singh KK, DiRienzo G, Drane L, Mao Y, Flood Z, Madison J, Ferreira M, Bergen S, King C, Sklar P, Sive H, Tsai LH

Common DISC1 polymorphisms disrupt Wnt/GSK3β-signaling and brain development

Neuron 2011; 72(4):545-558.

Singh Karun K, De Rienzo Gianluca, Drane Laurel, Mao Yingwei, Flood Zachary, Madison Jon, Ferreira Manuel, Bergen Sarah, King Cillian, Sklar Pamela, Sive Hazel, Tsai Li-Huei

Common DISC1 polymorphisms disrupt Wnt/GSK3β signaling and brain development.

Neuron 2011; 72(4):545-58.

Zhang D, Qian Y, Akula N, Alliey-Rodriguez N, Tang J, Gershon ES, Liu C

Accuracy of CNV Detection from GWAS Data

PLoS ONE 2011; 6(1):e14511.

Alvarado DM, Aferol H, McCall K, Huang JB, Techy M, Buchan J, Cady J, Gonzales PR, Dobbs MB, Gurnett CA

Familial Isolated Clubfoot Is Associated with Recurrent Chromosome 17q23.1q23.2 Microduplications Containing TBX4

American Journal of Human Genetics 2010; 87(1):154-160.

Bloch PJ, Weller AE, Doyle GA, Ferraro TN, Berrettini WH, Hodge R, Lohoff FW

Association analysis between polymorphisms in the myo-inositol monophosphatase 2 (IMPA2) gene and bipolar disorder

Progress in Neuro-Psychopharmacology and Biological Psychiatry 2010; 34(8):1515-1519.

Goes FS, Willour VL, Zandi PP, Belmonte PL, MacKinnon DF, Mondimore FM, Schweizer B, DePaulo JR Jr, Gershon ES, McMahon FJ, Potash JB

Sex-Specific Association of the Reelin Gene With Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 153B(2):549-553.

Huang J, Perlis RH, Lee PH, Rush AJ, Fava M, Sachs GS, Lieberman J, Hamilton SP, Sullivan P, Sklar P, Purcell S, Smoller JW

Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression

The American journal of psychiatry 2010; 167(10):10.1176/appi.ajp.2010.09091335.

Joo EJ, Greenwood TA, Schork N, McKinney RA, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR

Suggestive evidence for linkage of ADHD features in bipolar disorder to chromosome 10p14

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 153(1):260-268.

Knight J, Nanette Rochberg MA, Saccone SF, Nurnberger J, Rice JP

An investigation of candidate regions for association with Bipolar disorder

American Journal of Medical Genetics 2010; 153B(7):1292-1297.

Lohoff FW, Ferraro TN, Brodkin ES, Weller AE, Bloch PJ

Association between polymorphisms in the metallophosphoesterase (MPPE1) gene and bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 153B(3):830-836.

McMahon FJ, Akula N, Schulze TG, Muglia P, Tozzi F, Detera-Wadleigh SD, Steele CJ, Breuer R, Strohmaier J, Wendland JR, Mattheisen M, Mühleisen TW, Maier W, Nöthen MM, Cichon S, Farmer A, Vincent JB, Holsboer F, Preisig M, Rietschel M

Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1

Nature genetics 2010; 42(2):128-131.

Oedegaard KJ, Greenwood TA, Johansson S, Jacobsen KK, Halmoy A, Fasmer OB, Akiskal HS, Haavik J, Kelsoe JR

A Genome-wide Association Study of Bipolar Disorder and Co-morbid Migraine

Genes, brain, and behavior 2010; 9(7):673-680.

Oedegaard KJ, Greenwood TA, Lunde A, Fasmer OB, Akiskal HS, Kelsoe JR, NIMH Genetics Initiative Bipolar Disorder Consortium

A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11

Journal of affective disorders 2010; 122(1):14-26.

Perlis RH, Huang J, Purcell S, Fava M, Rush AJ, Sullivan PF, Hamilton SP, McMahon FJ, Schulze T, Potash JB, Zandi PP, Willour VL, Penninx BW, Boomsma DI, Vogelzangs N, Middeldorp CM, Rietschel M, Nöthen M, Cichon S, Gurling H, Bass N, McQuillin A, Hamshere M, Craddock N, Sklar P, Smoller JW

Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients

The American journal of psychiatry 2010; 167(12):1499-1507.

Zhang P, Xiang N, Chen Y, Œliwerska E, McInnis MG, Burmeister M, Zöllner S

Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs

Bipolar Disorders 2010; 12(8):786-792.

Goes FS, Willour VL, Zandi PP, Belmonte PL, MacKinnon DF, Mondimore FM, Schweizer B, Gershon ES, McMahon FJ, Potash JB

Family-Based Association Study of Neuregulin 1 With Psychotic Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 0(5):693-702.

Grover D, Verma R, Goes FS, Mahon PL, Gershon ES, McMahon FJ, Potash JB

Family-based association of YWHAH in psychotic bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 0(7):977-983.

Hamshere ML, Gordon-Smith K, Forty L, Jones L, Caesar S, Fraser C, Hyde S, Tredget J, Kirov G, Jones I

Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups

Journal of affective disorders 2009; 116(1):23-29.

Hoffmann TJ, Lange C, Vansteelandt S, Laird NM

Gene-Environment Interaction Tests for Dichotomous Traits in Trios and Sibships

Genetic epidemiology 2009; 33(8):691-699.

Johnson C, Drgon T, McMahon FJ, Uhl GR

Convergent genome wide association results for bipolar disorder and substance dependence

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150(2):182-190.

Kerner B, Jasinska AJ, Deyoung J, Almonte M, Choi OW, Freimer NB

Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150B(1):24-32.

Kripke DF, Nievergelt CM, Joo E, Shekhtman T, Kelsoe JR

Circadian polymorphisms associated with affective disorders

Journal of Circadian Rhythms 2009; 7:2.

Maheshwari M, Shi J, Badner JA, Skol A, Willour VL, Muzny DM, Wheeler DA, Gerald FR, Detera-Wadleigh S, McMahon FJ, Potash JB, Gershon ES, Liu C, Gibbs RA

Common and Rare Variants of DAOA in Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150B(7):960-966.

Mansour HA, Talkowski ME, Wood J, Chowdari KV, McClain L, Prasad K, Montrose D, Fagiolini A, Friedman ES, Allen MH, Bowden CL, Calabrese J, El-Mallakh RS, Escamilla M, Faraone SV, Fossey MD, Gyulai L, Loftis JM, Hauser P, Ketter TA, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel J, Sachs GS, Sklar P, Smoller JW, Laird N, Keshavan M, Thase ME, Axelson D, Birmaher B, Lewis D, Monk T, Frank E, Kupfer DJ, Devlin B, Nimgaonkar VL

Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia

Bipolar Disorders 2009; 11(7):701-710.

Payne JL, Klein SR, Zamoiski RB, Zandi PP, Bienvenu OJ, MacKinnon DF, Mondimore FM, Schweizer B, Swartz KL, Crowe RP, Scheftner WA, Weissman MM, Levinson DF, DePaulo JR Jr, Potash JB

Premenstrual mood symptoms: study of familiality and personality correlates in mood disorder pedigrees

Archives of women's mental health 2009; 12(1):10.1007/s00737-008-0043-4.

Perlis Roy H, Smoller Jordan W, Ferreira Manuel A R, McQuillin Andrew, Bass Nick, Lawrence Jacob, Sachs Gary S, Nimgaonkar Vishwajit, Scolnick Edward M, Gurling Hugh, Sklar Pamela, Purcell Shaun

A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder.

The American journal of psychiatry 2009; 166(6):718-25.

Saunders EFH, Zhang P, Copeland JN, Mclnnis MG, Zöllner S

Suggestive linkage at 9p22 in bipolar disorder weighted by alcohol abuse

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150(8):1133-1138.

Schulze T, Detera-Wadleigh S, Akula N, Gupta A, Kassem L, Steele J, Pearl J, Strohmaier J, Breuer R, Schwarz M, Propping P, Nöthen M, Cichon S, Schumacher J, Rietschel M, McMahon F

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

Molecular psychiatry 2009; 14(5):487-491.

Scott LJ, Muglia P, Kong XQ, Guan W, Flickinger M, Upmanyu R, Tozzi F, Li JZ, Burmeister M, Absher D, Thompson RC, Francks C, Meng F, Antoniades A, Southwick AM, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Day R, Matthews K, McGuffin P, Strauss JS, Kennedy JL, Middleton L, Roses AD, Watson SJ, Vincent JB, Myers RM, Farmer AE, Akil H, Burns DK, Boehnke M

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

Proceedings of the National Academy of Sciences of the United States of America 2009; 106(18):7501-7506.

Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, Koller DL, Lawson WB, Liu C, Lohoff F, McInnis MG, McMahon FJ, Mirel DB, Nievergelt C, Nurnberger J, Nwulia EA, Paschall J, Potash JB, Rice J, Schulze TG, Scheftner W, Panganiban C, Zaitlen N, Zandi PP, Zöllner S, Schork NJ, Kelsoe JR

GENOME-WIDE ASSOCIATION STUDY OF BIPOLAR DISORDER IN EUROPEAN AMERICAN AND AFRICAN AMERICAN INDIVIDUALS

Molecular psychiatry 2009; 14(8):755-763.

Washizuka S, Iwamoto K, Kakiuchi C, Bundo M, Kato T

Expression of mitochondrial complex I subunit gene NDUFV2 in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia

Neuroscience research 2009; 63(3):199-204.

Willour V, Chen H, Toolan J, Belmonte P, Cutler D, Goes F, Zandi P, Lee R, MacKinnon D, Mondimore F, Schweizer B, DePaulo J Jr, Gershon E, McMahon F, Potash J

Family-based association of FKBP5 in bipolar disorder

Molecular psychiatry 2009; 14(3):261-268.

Zhou X, Tang W, Greenwood TA, Guo S, He L, Geyer MA, Kelsoe JR

Transcription Factor SP4 Is a Susceptibility Gene for Bipolar Disorder

PLoS ONE 2009; 4(4):e5196.

Baum A, Akula N, Cabanero M, Cardona I, Corona W, Klemens B, Schulze T, Cichon S, Rietschel M, Nöthen M, Georgi A, Schumacher J, Schwarz M, Jamra RA, Höfels S, Propping P, Satagopan J, Detera-Wadleigh S, Hardy J, McMahon F

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Molecular psychiatry 2008; 13(2):197-207.

Escamilla MA, Zavala JM

Genetics of bipolar disorder

Dialogues in Clinical Neuroscience 2008; 10(2):141-152.

Lohoff FW, Bloch PJ, Weller AE, Ferraro TN, Berrettini WH

Association analysis of the pituitary adenylate cyclase-activating polypeptide (PACAP/ADCYAP1) gene in bipolar disorder

Psychiatric genetics 2008; 18(2):53-58.

Lohoff FW, Weller AE, Bloch PJ, Nall AH, Ferraro TN, Berrettini WH

Association between polymorphisms in the vesicle-associated membrane protein-associated protein A (VAPA) gene on chromosome 18p and bipolar disorder

Journal of Neural Transmission 2008; 115(9):1339-1345.

Nwulia EA, Zandi PP, McInnis MG, DePaulo Jr R, MacKinnon DF

Rapid switching of mood in families with familial bipolar disorder

Bipolar disorders 2008; 10(5):597-606.

Payne JL, MacKinnon DF, Mondimore FM, McInnis MG, Schweizer B, Zamoiski RB, McMahon FJ, Nurnberger JI, Rice JP, Scheftner W

Familial aggregation of postpartum mood symptoms in bipolar disorder pedigrees

Bipolar disorders 2008; 10(1):38-44.

Perlis RH, Purcell S, Fagerness J, Kirby A, Petryshen TL, Fan J, Sklar P

Family-based association study of lithium-related and other candidate genes in bipolar disorder

Archives of general psychiatry 2008; 65(1):53-61.

Potash JB, Buervenich S, Cox NJ, Zandi PP, Akula N, Steele J, Rathe JA, Avramopoulos D, Detera-Wadleigh SD, Gershon ES

Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12. 3: Association with HMG2L1 and TOM1

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147(1):59-67.

Ross J, Berrettini W, Coryell W, Gershon ES, Badner JA, Kelsoe JR, McInnis MG, McMahon FJ, Murphy DL, Nurnberger JI Jr, Foroud T, Rice JP, Scheftner WB, Zandi P, Edenberg H, Byerley W

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

Psychiatric genetics 2008; 18(4):191-198.

Saunders EH, Scott LJ, McInnis MG, Burmeister M

Familiality and diagnostic patterns of subphenotypes in the National Institutes of Mental Health bipolar sample

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147(1):18-26.

Shi J, Badner JA, Liu C

PDLIM5 and susceptibility to bipolar disorder: a family-based association study and meta-analysis

Psychiatric genetics 2008; 18(3):116-121.

Shi J, Badner JA, Hattori E, Potash JB, Willour VL, McMahon FJ, Gershon ES, Liu C

Neurotransmission and Bipolar Disorder: A Systematic Family-based Association Study

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(7):1270-1277.

Shi J, Wittke-Thompson JK, Badner JA, Hattori E, Potash JB, Willour VL, McMahon FJ, Gershon ES, Liu C

Clock Genes may Influence Bipolar Disorder Susceptibility and Dysfunctional Circadian Rhythm

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(7):1047-1055.

Sklar P, Smoller J, Fan J, Ferreira M, Perlis R, Chambert K, Nimgaonkar V, McQueen M, Faraone S, Kirby A, de Bakker P, Ogdie M, Thase M, Sachs G, Todd-Brown K, Gabriel S, Sougnez C, Gates C, Blumenstiel B, Defelice M, Ardlie K, Franklin J, Muir W, McGhee K, MacIntyre D, McLean A, VanBeck M, McQuillin A, Bass N, Robinson M, Lawrence J, Anjorin A, Curtis D, Scolnick E, Daly M, Blackwood D, Gurling H, Purcell S

Whole-genome Association Study of Bipolar Disorder

Molecular psychiatry 2008; 13(6):558-569.

Zandi PP, Belmonte PL, Willour VL, Goes FS, Badner JA, Simpson SG, Gershon ES, McMahon FJ, DePaulo JR Jr, Potash JB

Association Study of Wnt Signaling Pathway Genes in Bipolar Disorder

Archives of general psychiatry 2008; 65(7):785-793.

Zandi PP, Zoellner S, Avramopoulos D, Willour VL, Chen Y, Qin ZS, Burmeister M, Miao K, Gopalakrishnan S, McEachin R, Potash JB, DePaulo JR Jr, McInnis MG

Family-based SNP Association Study on 8q24 in Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(5):612-618.

Barrett TB, Emberton JE, Nievergelt CM, Liang SG, Hauger RL, Eskin E, Schork NJ, Kelsoe JR

Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation

Psychiatric genetics 2007; 17(6):315-322.

Baum AE, Akula N, Cabanero M, Cardona I, Corona W, Klemens B, Schulze TG, Cichon S, Rietschel M, Nöthen MM, Georgi A, Schumacher J, Schwarz M, Abou Jamra R, Höfels S, Propping P, Satagopan J, NIMH Genetics Initiative Bipolar Disorder Consortium, Detera-Wadleigh SD, Hardy J, McMahon FJ

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Mol Psychiatry 2007; 1-11.

Detera-Wadleigh SD, Liu C, Maheshwari M, Cardona I, Corona W, Akula N, Steele CJM, Badner JA, Kundu M, Kassem L

Sequence variation in DOCK9 and heterogeneity in bipolar disorder

Psychiatric genetics 2007; 17(5):274-286.

Goes FS, Zandi PP, Miao K, McMahon FJ, Steele J, Willour VL, MacKinnon DF, Mondimore FM, Schweizer B, Nurnberger Jr JI, Rice JP, Scheftner W, Coryell W, Berrettini WH, Kelsoe JR, Byerley W, Murphy DL, Gershon ES, Bipolar Disorder Phenome Group, DePaulo Jr JR, McInnis MG, Potash JP

Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33

American Journal of Psychiatry 2007; 164(2):236-247.

Goes FS, Sadler B, Toolan J, Zamoiski RD, Mondimore FM, MacKinnon DF, Schweizer B, Raymond DePaulo J, Potash JB

Psychotic features in bipolar and unipolar depression

Bipolar disorders 2007; 9(8):901-906.

Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Yamada K, Yoshikawa T

Association analysis of ATF4 and ATF5, genes for interacting-proteins of DISC1, in bipolar disorder

Neuroscience letters 2007; 417(3):316-321.

Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Umekage T, Tochigi M

Association analysis of HSP90B1 with bipolar disorder

Journal of human genetics 2007; 52(10):794-803.

Lopez VA, Detera-Wadleigh S, Cardona I, Kassem L, McMahon FJ, National Institute of Mental Health Genetics Initiative Bipolar Disorder Consortium

Nested association between genetic variation in tryptophan hydroxylase II, bipolar affective disorder, and suicide attempts

Biological psychiatry 2007; 61(2):181-186.

MacKinnon DF, Craighead B, Hoehn-Saric R

Carbon Dioxide Provocation of Anxiety and Respiratory Response in Bipolar Disorder

Journal of affective disorders 2007; 99(1-3):45-49.

Payne JL, Roy PS, Murphy-Eberenz K, Weismann MM, Swartz KL, McInnis MG, Nwulia E, Mondimore FM, MacKinnon DF, Miller EB

Reproductive cycle-associated mood symptoms in women with major depression and bipolar disorder

Journal of affective disorders 2007; 99(1):221-229.

Potash JB, Toolan J, Steele J, Eng B, Miller EB, Pearl J, Zandi PP, Schulze TG, Kassem L, Simpson SG

The bipolar disorder phenome database: a resource for genetic studies

The American journal of psychiatry 2007; 164(8):1229-1237.

Potash JB, Toolan J, Steele J, Miller EB, Pearl J, Zandi PP, Schulze TG, Kassem L, Simpson SG, Lopez V

Base de datos del fenoma del trastorno bipolar: un recurso para estudios genéticos.

American Journal of Psychiatry-Edición Española 2007; 10(10):.

Savitz J, Cupido CL, Ramesar RK

Preliminary evidence for linkage to chromosome 1q31-32, 10q23. 3, and 16p13. 3 in a South African cohort with bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(3):383-387.

Schiffer HH, Heinemann SF

Association of the human kainate receptor GluR7 gene (GRIK3) with recurrent major depressive disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(1):20-26.

Shi J, Hattori E, Zou H, Badner JA, Christian SL, Gershon ES, Liu C

No Evidence for Association between 19 Cholinergic Genes and Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144B(6):715-723.

Zandi PP, Avramopoulos D, Willour VL, Huo Y, Miao K, MacKinnon DF, McInnis MG, Potash JB, DePaulo JR

SNP fine mapping of chromosome 8q24 in bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(5):625-630.

Baysal BE, Willett-Brozick JE, Bacanu SA, Detera-Wadleigh S, Nimgaonkar VL

Common variations in ALG9 are not associated with bipolar I disorder: a family-based study

Behavioral and Brain Functions 2006; 2:25.

Boehnke M, Skol A, Scott L, Abecasis G, Li J, Thompson RC, Meng F, Guan W, Absher D, Akil H

Design and analysis of two-stage association studies: application to bipolar I.

Cheng R, Juo SH, Loth JE, Nee J, Iossifov I, Blumenthal R, Sharpe L, Kanyas K, Lerer B, Lilliston B

Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder

Molecular psychiatry 2006; 11(3):252-260.

Hayden EP, Nurnberger JI

Genetics of bipolar disorder

Bipolar Depression. A Comprehensive Guide 2006; 69-100.

Kassem L, Lopez V, Hedeker D, Steele J, Zandi P, NIMH Genetics Initiative Bipolar Disorder Consortium, McMahon FJ

Familiality of polarity at illness onset in bipolar affective disorder

American Journal of Psychiatry 2006; 163(10):1754-1759.

Lohoff FW, Dahl JP, Ferraro TN, Arnold SE, Gallinat J, Sander T, Berrettini WH

Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar I disorder

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2006; 31(12):2739-2747.

Mansour HA, Wood J, Logue T, Chowdari KV, Dayal M, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL

Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia

Genes, brain and behavior 2006; 5(2):150-157.

McQueen MB, Blacker D, Laird NM

Variance Calculations for Identity-by-Descent Estimation

American Journal of Human Genetics 2006; 78(6):914-921.

McQuillin A, Bass NJ, Kalsi G, Lawrence J, Puri V, Choudhury K, Detera-Wadleigh SD, Curtis D, Gurling HMD

Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22. 3

Molecular psychiatry 2006; 11(2):134-142.

Nakatani N, Hattori E, Ohnishi T, Dean B, Iwayama Y, Matsumoto I, Kato T, Osumi N, Higuchi T, Niwa SI

Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation

Human molecular genetics 2006; 15(12):1949-1962.

Nievergelt CM, Kripke DF, Barrett TB, Burg E, Remick RA, Sadovnick AD, McElroy SL, Keck PE Jr, Schork NJ, Kelsoe JR

Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2006; 141B(3):234-241.

Weller AE, Dahl JP, Lohoff FW, Ferraro TN, Berrettini WH

Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder

Psychiatric genetics 2006; 16(1):3-8.

Akiskal HS, Mendlowicz MV, Girardin J-L, Rapaport MH, Kelsoe JR, Gillin JC, Smith TL

TEMPS-A: validation of a short version of a self-rated instrument designed to measure variations in temperament

J Affect Disord 2005; 85:45-52.

Evans L, Akiskal HS, Keck PE, McElroy SL, Sadovnick AD, Remick RA, Kelsoe JR

Familiality of temperament in bipolar disorder: Support for a genetic spectrum

J Affect Disord 2005; 85:153-168.

Ferraren DO, Liu C, Badner JA, Corona W, Rezvani A, Monje VD, Gershon ES, Bonner TI, Detera-Wadleigh SD

Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 133(1):12-17.

Hawton K, Sutton L, Haw C, Sinclair J, Harriss L

Suicide and attempted suicide in bipolar disorder: a systematic review of risk factors

Journal of Clinical Psychiatry 2005; 66(6):693-704.

Kakiuchi C, Ishiwata M, Nanko S, Kunugi H, Minabe Y, Nakamura K, Mori N, Fujii K, Umekage T, Tochigi M

Functional polymorphisms of HSPA5: possible association with bipolar disorder

Biochemical and biophysical research communications 2005; 336(4):1136-1143.

Krishnan KRR

Psychiatric and medical comorbidities of bipolar disorder

Psychosomatic medicine 2005; 67(1):1-8.

Lachman HM, Stopkova P, Rafael MA, Saito T

Association of schizophrenia in African Americans to polymorphism in synapsin III gene

Psychiatric genetics 2005; 15(2):127-132.

Lin PI, McInnis MG, Potash JB, Willour VL, MacKinnon DF, Miao K, DePaulo JR, Zandi PP

Assessment of the Effect of Age at Onset on Linkage to Bipolar Disorder: Evidence on Chromosomes 18p and 21q

American Journal of Human Genetics 2005; 77(4):545-555.

Lohoff FW, Sander T, Ferraro TN, Dahl JP, Gallinat J, Berrettini WH

Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 139(1):51-53.

Lohoff FW, Ferraro TN, McNabb L, Schwebel C, Dahl JP, Doyle GA, Buono RJ, Berrettini WH

No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder

Psychiatry research 2005; 135(3):171-177.

Lohoff FW, Berrettini WH

Lack of association between variations in the melanocortin 5 receptor gene and bipolar disorder

Psychiatric genetics 2005; 15(4):255-258.

Lyons-Warren A, Chang JJ, Balkissoon R, Kamiya A, Garant M, Nurnberger J, Scheftner W, Reich T, McMahon F, Kelsoe J

Evidence of association between bipolar disorder and Citron on chromosome 12q24

Molecular psychiatry 2005; 10(9):807-809.

MacKinnon DF, Potash JB, McMahon FJ, Simpson SG, Raymond DePaulo J, Zandi PP

Rapid mood switching and suicidality in familial bipolar disorder

Bipolar disorders 2005; 7(5):441-448.

Mansour HA, Talkowski ME, Wood J, Pless L, Bamne M, Chowdari KV, Allen M, Bowden CL, Calabrese J, El-Mallakh RS

Serotonin gene polymorphisms and bipolar I disorder: focus on the serotonin transporter

Annals of medicine 2005; 37(8):590-602.

Mansour A, Monk TH, Nimgaonkar VL

Circadian genes and bipolar disorder

Trends Mol Med 2005; 37:196-205.

Mcnabb L, Ballas C, Doyle GA, Scena JE, Moore KW, Buono R, Berrettini WH

Association analysis of CHMP1.5 genetic variation and bipolar disorder

Psychiatr Genet 2005; 15:211-214.

McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, Coryell W, Craddock N, Daly MJ, DePaulo JR, Edenberg HJ, Foroud T, Gill M, Gilliam TC, Hamshere M, Jones I, Jones L, Juo SH, Kelsoe JR, Lambert D, Lange C, Lerer B, Liu J, Maier W, MacKinnon JD, McInnis MG, McMahon FJ, Murphy DL, Nöthen MM, Nurnberger JI, Pato CN, Pato MT, Potash JB, Propping P, Pulver AE, Rice JP, Rietschel M, Scheftner W, Schumacher J, Segurado R, Van Steen K, Xie W, Zandi PP, Laird NM

Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q

American Journal of Human Genetics 2005; 77(4):582-595.

Mendlowicz MV, Girardin J-L, Kelsoe JR, Akiskal HS

A comparison of recovered bipolar patients, healthy relatives of bipolar probands, and normal controls using the short TEMPS-A

J Affect Disord 2005; 85:147-151.

Nievergelt CM, Kripke DF, Remick RA, Sadovnick AD, McElroy SL, Keck PR, Kelsoe JR

Examination of the clock gene Cryptochrome 1 in bipolar disorder: mutational analysis and absence of evidence for linkage or association

Psychiatr Genet 2005; 15(1):45-52.

Nurnberger JI

Meeting Report for Molecular Psychiatry, 2005

Psychiatric Genetics 2005; 15(4):241-242.

Pato CN, Middleton FA, Gentile KL, Morley CP, Medeiros H, Macedo A, Azevedo MH, Pato MT

Genetic linkage of bipolar disorder to chromosome 6q22 is a consistent finding in Portuguese subpopulations and may generalize to broader populations

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 134(1):119-121.

Stopkova P, Vevera J, Paclt I, Zukov I, Papolos DF, Saito T, Lachman HM

Screening of PIP5K2A promoter region for mutations in bipolar disorder and schizophrenia

Psychiatric genetics 2005; 15(3):223-227.

Cichon S, Buervenich S, Kirov G, Akula N, Dimitrova A, Green E, Schumacher J, Klopp N, Becker T, Ohlraun S

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

Nature genetics 2004; 36(8):783-784.

Faraone SV, Su J, Tsuang MT

A genome-wide scan of symptom dimensions in bipolar disorder pedigrees of adult probands

Journal of affective disorders 2004; 82:S71-S78.

Horiuchi Y, Nakayama J, Ishiguro H, Ohtsuki T, Detera-Wadleigh SD, Toyota T, Yamada K, Nankai M, Shibuya H, Yoshikawa T

Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders

Biological psychiatry 2004; 55(1):40-45.

Iwamoto K, Bundo M, Washizuka S, Kakiuchi C, Kato T

Expression of HSPF1 and LIM in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia

Journal of human genetics 2004; 49(5):227-231.

Mendlowicz MV, Akiskal HS, Kelsoe JR, Rapaport MH, Jean-Louis G, Gillin JC

Temperament in the clinical differentiation of depressed bipolar and unipolar major depressive patients

J Affect Disord 2004

Petti T, Reich W, Todd RD, Joshi P, Galvin M, Reich T, Raymond DePaulo J, Nurnberger J

Psychosocial variables in children and teens of extended families identified through bipolar affective disorder probands

Bipolar Disorders 2004; 6(2):106-114.

Prathikanti S, Schulze TG, Chen YS, Harr B, Akula N, Hennessy K, Potluri S, Lyons J, Nguyen T, McMahon FJ

Neither single-marker nor haplotype analyses support an association between genetic variation near NOTCH4 and bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 131(1):10-15.

Schulze TG, Buervenich S, Badner JA, Steele CJM, Detera-Wadleigh SD, Dick D, Foroud T, Cox NJ, MacKinnon DF, Potash JB

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Biological psychiatry 2004; 56(1):18-23.

Washizuka S, Iwamoto K, Kazuno A, Kakiuchi C, Mori K, Kametani M, Yamada K, Kunugi H, Tajima O, Akiyama T

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees

Biological psychiatry 2004; 56(7):483-489.

Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL, Moe PR, Samavedy N, El-Mallakh R, Manji H, Glitz DA, Meyer ET, Smiley C, Hahn R, Widmark C, McKinney R, Sutton L, Ballas C, Grice D, Berrettini W, Byerley W, Coryell W, DePaulo R, MacKinnon DF, Gershon ES, Kelsoe JR, McMahon FJ, McInnis M, Murphy DL, Reich T, Scheftner W, Nurnberger Jr. JI

Genomewide Linkage Analyses of Bipolar Disorder: A New Sample of 250 Pedigrees from the National Institute of Mental Health Genetics Initiative

American Journal of Human Genetics 2003; 73(1):107-114.

Hattori E, Liu C, Badner JA, Bonner TI, Christian SL, Maheshwari M, Detera-Wadleigh SD, Gibbs RA, Gershon ES

Polymorphisms at the G72/G30 Gene Locus, on 13q33, Are Associated with Bipolar Disorder in Two Independent Pedigree Series

American Journal of Human Genetics 2003; 72(5):1131-1140.

Itokawa M, Yamada K, Iwayama-Shigeno Y, Ishitsuka Y, Detera-Wadleigh S, Yoshikawa T

Genetic analysis of a functional GRIN2A promoter (GT) n repeat in bipolar disorder pedigrees in humans

Neuroscience letters 2003; 345(1):53-56.

Kakiuchi C, Iwamoto K, Ishiwata M, Bundo M, Kasahara T, Kusumi I, Tsujita T, Okazaki Y, Nanko S, Kunugi H, Sasaki T, Kato T

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

Nat Genet 2003; 35(2):171-5.

Kelsoe JR

Arguments for the genetic basis of the bipolar spectrum

J Affective Disord 2003; 73:183-197.

Kelsoe JR

Update on the search for genes for bipolar disorder

Current Psychosis and Therapeutics Reports 2003; 1:62-66.

MacKinnon DF, Zandi PP, Gershon E, Nurnberger JI, Reich T, DePaulo JR

Rapid switching of mood in families with multiple cases of bipolar disorder

Archives of general psychiatry 2003; 60(9):921-928.

MacKinnon DF, Zandi PP, Gershon ES, Nurnberger Jr JI, DePaulo Jr JR

Association of rapid mood switching with panic disorder and familial panic risk in familial bipolar disorder

American Journal of Psychiatry 2003; 160(9):1696-1698.

McInnis MG, Dick DM, Willour VL, Avramopoulos D, MacKinnon DF, Simpson SG, Potash JB, Edenberg HJ, Bowman ES, McMahon FJ

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

Biological psychiatry 2003; 54(11):1265-1273.

Potash JB, Chiu YF, MacKinnon DF, Miller EB, Simpson SG, McMahon FJ, McInnis MG, DePaulo JR

Familial aggregation of psychotic symptoms in a replication set of 69 bipolar disorder pedigrees

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 116(1):90-97.

Badner JA, Gershon ES

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

Molecular psychiatry 2002; 7(4):405-411.

Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD

A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family

Neurogenetics 2002; 4(1):43-53.

Greenwood TA, Alexander M, Keck PE, McElroy S, Sadovnick AD, Remick RA, Shaw SH, Kelsoe JR

Segmental linkage disequilibrium within the dopamine transporter gene

Molecular psychiatry 2002; 7(2):165-173.

Liang SG, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Kelsoe JR

A linkage disequilibrium study of bipolar disorder and microsatellite markers on 22q13

Psychiatric genetics 2002; 12(4):231-235.

Shilling PD, Kelsoe JR

Functional genomics approaches to understanding brain disorders

Pharmacogenomics 2002; 3(1):31-47.

Sipe, JC, Chiang K, Gerber A, Beutler E, Cravatt BF

A missense mutation in human fatty acid amide hydrolase associated with problem drug use

Proceedings of the National Academy of Sciences of the United States of America 2002; 99(12):8394-8399.

Sklar P, Gabriel SB, McInnis MG, Bennet P, Lim YM, Tsan G, Schaffner S, Kirov G, Jones I, Owen M

Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus.

Molecular psychiatry 2002; 7(6):.

Sklar P

Linkage analysis in psychiatric disorders: the emerging picture

Annual review of genomics and human genetics 2002; 3(1):371-413.

Baron M

Genetic linkage and bipolar disorder: a cautionary note

Journal of affective disorders 2001; 67(1):267-273.

Dick DM, Nurnberger JI, Edenberg HJ, McInnis MG, Reich T, Gershon ES, Foroud TM

Replication of suggestive linkage on chromosomes 5 and 16 in the NIMH genetics initiative bipolar pedigrees

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2001; 105(7):592.

Greenwood TA, Alexander M, Keck PE, McElroy S, Sadovnick AD, Remick RA, Kelsoe JR

Evidence for linkage disequilibrium between the dopamine transporter and bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2001; 105:145-151.

Kelsoe JR, Spence MA, Loetscher E, Foguet M, Sadovnick AD, Remick RA, Flodman P, Khristich J, Mroczkowski-Parker Z, Brown JL, Masser D, Ungerleider S, Rapaport MH, Wishart WL, Luebbert H

A genome survey indicates a susceptibility locus for bipolar disorder on chromosome 22

Proceedings of the National Academy of Sciences of the United States of America 2001; 98(2):585-590.

Nurnberger Jr JI

Park City, Utah Molecular Psychiatry Meeting, February 2001

Psychiatric genetics 2001; 11(1):1-4.

Corbett J, Rice J, Saccone N, Goate A, Reich T, Foroud T, Nurnberger J, Edenberg H, DePaulo JR, Gershon E

Further analyses of the NIMH bipolar dataset

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2000; 96(4):469.

Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees

American journal of medical genetics 2000; 96(1):18-23.

Freedman R, Adams CE, Adler LE, Bickford PC, Gault J, Harris JG, Nagamoto HT, Olincy A, Ross RG, Stevens KE

Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophrenia

American journal of medical genetics 2000; 97(1):58-64.

McInnis MG, Swift-Scanlanl T, Mahoney AT, Vincent J, Verheyen G, Lan TH, Oruc L, Riess O, Van Broeckhoven C, Chen H

Allelic distribution of CTG18. 1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia

Molecular psychiatry 2000; 5(4):439-442.

Niculescu AB, Segal DS, Kuczenski R, Barrett T, Hauger RL, Kelsoe JR

Identifying a series of candidate genes for mania and psychosis: A convergent functional genomics approach

Physiol Genomics 2000; 4:83-91.

Saito T, Parsia S, Papolos DF, Lachman HM

Analysis of the pseudoautosomal X-linked gene SYBL1in bipolar affective disorder: Description of a new candidate allele for psychiatric disorders

American journal of medical genetics 2000; 96(3):317-323.

Kelsoe JR

Recent progress in the search for genes for bipolar disorder

Current psychiatry reports 1999; 1(2):135-140.

Blehar MC, DePaulo Jr JR, Gershon ES, Reich T

Women with bipolar disorder: findings from the NIMH Genetics Initiative sample

Psychopharmacology Bulletin 1998; 34(3):239.

Foroud TM, Castellucio PF, Koller DL, Edenberg HJ, Goate A, Detera-Wadleigh S, Stine OC, McMahon FJ, McInnis MG, Rice J

Genomewide scan of affected relative pairs using the NIMH Genetics Initiative bipolar affective disorder pedigrees

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81(6):462.

Detera-Wadleigh SD, Badner JA, Yoshikawa T, Sanders AR, Goldin LR, Turner G, Rollins DY, Moses T, Guroff JJ, Kazuba D

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q

American journal of medical genetics 1997; 74(3):254-262.

Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C, Willig C, Zhao J, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Rice JP, Goate A, Reich T, Stine OC, McMahon F, DePaulo JR, Meyers D, Detra-Wadleigh SD, Goldin LR, Gershon ES, Blehar MC, Nurnberger JI Jr

Initial Genomic Scan of the NIMH Genetics Initiative Bipolar Pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1997; 74:238-246.

Rice JP, Goate A, Williams JT, Bierut L, Dorr D, Wu W, Shears S, Gopalakrishnan G, Edenberg HJ, Foroud T

Initial Genome Scan of the NIMH Genetics Initiative Bipolar Pedigrees: Chromosomes 1, 6, 8

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1997; 74:247-253.

Stine OC, McMahon FJ, Chen L-S, Xu J, Meyers DA, MacKinnon DF, Simpson S, McInnis MG, Rice JP, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI, Detera-Wadleigh SD, Goldin LR, Guroff J, Gershon, ES, Blehar MC, DePaulo JR

Initial genome screen for bipolar disorder in the NIMH Genetics Initiative pedigrees: Chromosomes 2, 11, 13, 14 and X

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1997; 74:263-269.

The NIMH Genetics Initiative Bipolar Group: Nurnberger JI, DePaulo JR, Gershon ES, Reich T, Blehar MC, collaborators from Indiana University, HJ Edenberg, T Faroud, M Miller, E Bowman, A Mayeda, NL Rau, C Smiley, PM Conneally, Johns Hopkins University, F McMahon, D Meyers, S Simpson, M McInnis, OC Stine), the NIMH Intramural Program, SD Datera-Wadleigh, LR Goldin, JJ Guroff, ME Maxwell, D Kazuba, PV Gejman, J Badner, A Sanders, Washington University, JP Rice, L Bierut, A Goate

A genomic survey of bipolar illness in the NIMH Genetics Initiative pedigrees: A preliminary report

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1997; 74(3):227-237.

Blehar MC, Faraone SV, Zeller PJ, Nurnberger JI, Tsuang MT, Kirch DG, Shore D, Gershefski JMA, Reich T, Cloninger CR, Rau NL, DePaulo JR, Kaufmann CA, Harkavy-Friedman J, Malaspina D, Weise RE

Differentiation of schizoaffective bipolar disorder from bipolar disorder and schizophrenia

Depression 1996; 3(6):309-315.

Faraone SV, Blehar M, Pepple J, Moldin SO, Norton J, Nurnberger JI, Malaspina D, Kaufmann CA, Reich T, Cloninger CR

Diagnostic accuracy and confusability analyses: an application to the Diagnostic Interview for Genetic Studies

Psychological medicine 1996; 26(02):401-410.

Stewart L, Hall AL, Kang SHL, Shaw CA, Beaudet AL

Supplemental Methods

Brain Function

Nooner KB, Colcombe SJ, Tobe RH, Mennes M, Benedict MM, Moreno AL, Panek LJ, Brown S, Zavitz ST, Li Q, Sikka S, Gutman D, Bangaru S, Schlachter RT, Kamiel SM, Anwar AR, Hinz CM, Kaplan MS, Rachlin AB, Adelsberg S, Cheung B, Khanuja R, Yan C, Craddock CC, Calhoun V, Courtney W, King M, Wood D, Cox CL, Kelly AM, Di Martino A, Petkova E, Reiss PT, Duan N, Thomsen D, Biswal B, Coffey B, Hoptman MJ, Javitt DC, Pomara N, Sidtis JJ, Koplewicz HS, Castellanos FX, Leventhal BL, Milham MP

The NKI-Rockland Sample: A Model for Accelerating the Pace of Discovery Science in Psychiatry

Front Neurosci 2012; 6:152.

Nicholson G, Lenk GM, Reddel SW, Grant AE, Towne CF, Ferguson CJ, Simpson E, Scheuerle A, Yasick M, Hoffman S, Blouin R, Brandt C, Coppola G, Biesecker LG, Batish SD, Meisler MH

Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4

Brain 2011; 134(7):1959-1971.

Stewart LR, Hall AL, Kang SHL, Shaw CA, Beaudet AL

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

BMC medical genetics 2011; 12(1):154.

Lohoff FW, Bloch PJ, Weller AE, Nall AH, Doyle GA, Buono RJ, Ferraro TN, Kampman KM, Pettinati HM, Dackis CA, Oslin DW, O'Brien CP, Berrettini WH

Genetic variants in the cocaine- and amphetamine-regulated transcript gene (CARTPT) and cocaine dependence

Neuroscience letters 2008; 440(3):280-283.

Talati A, Fyer AJ, Weissman MM

A comparison between screened NIMH and clinically interviewed control samples on neuroticism and extraversion

Molecular psychiatry 2008; 13(2):122-130.

Freedman R, Ross R, Leonard S, Myles-Worsley M, Adams CE, Waldo M, Tregellas J, Martin L, Olincy A, Tanabe J, Kisley MA, Hunter S, Stevens KE

Early biomarkers of psychosis

Dialogues in Clinical Neuroscience 2005; 7(1):17-29.

Merikangas KR, Chakravarti A, Moldin SO, Araj H, Blangero J, Burmeister M, Crabbe JC, Depaulo JR, Foulks E, Freimer NB

Future of genetics of mood disorders research

Biological psychiatry 2002; 52(6):457-477.

Moe PR, Nurnberger J, Meyer ET, Wildblood R

Alcohol use and dependence in parents and offspring

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2001; 105(7):628.

Nurnberger J, Meyer ET, Flury L, Hu K, Foroud T

Alcoholism and mania

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2001; 105(7):567.

CommonMind Consortium

Eissman JM, Dumitrescu L, Mahoney ER, Smith AN, Mukherjee S, Lee ML, Scollard P, Choi SE, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski CC, Hernandez Saucedo H, Widaman KF, Buckley RF, Properzi MJ, Mormino EC, Yang HS, Harrison TM, Hedden T, Nho K, Andrews SJ, Tommet D, Hadad N, Sanders RE, Ruderfer DM, Gifford KA, Zhong X, Raghavan NS, Vardarajan BN, Pericak-Vance MA, Farrer LA, Wang LS, Cruchaga C, Schellenberg GD, Cox NJ, Haines JL, Keene CD, Saykin AJ, Larson EB, Sperling RA, Mayeux R, Cuccaro ML, Bennett DA, Schneider JA, Crane PK, Jefferson AL, Hohman TJ

Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease

Brain 2022; 145(7):2541-2554.

Li Y, Ma C, Li S, Wang J, Li W, Yang Y, Li X, Liu J, Yang J, Liu Y, Li K, Li J, Huang D, Chen R, Lv L, Xiao X, Li M, Luo X

Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression

Advanced Science 2022; 9(6):2104786.

Li S, Li J, Liu J, Wang J, Li X, Huo Y, Li Y, Liu Y, Li M, Xiao X, Luo XJ

Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression

Brain 2021; 145(2):770-786.

Li X, Su X, Liu J, Li H, Li M, Li W, Luo XJ

Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

Translational Psychiatry 2021; 11:306.

Liu Y, Qu HQ, Chang X, Tian L, Qu J, Glessner J, Sleiman PM, Hakonarson H

Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters

International Journal of Molecular Sciences 2021; 22(7):3364.

Liu J, Li S, Li X, Li W, Yang Y, Guo S, Lv L, Xiao X, Yao YG, Guan F, Li M, Luo XJ

Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia

BMC Medicine 2021; 19:177.

Pai S, Weber P, Isserlin R, Kaka H, Hui S, Shah MA, Giudice L, Giugno R, Nøhr AK, Baumbach J, Bader GD

netDx: Software for building interpretable patient classifiers by multi-'omic data integration using patient similarity networks

F1000Research 2021; 9:1239.

Qiu Y, Wang J, Lei J, Roeder K

Identification of cell-type-specific marker genes from co-expression patterns in tissue samples

Bioinformatics 2021; 37(19):3228-3234.

Tavares V, Monteiro J, Vassos E, Coleman J, Prata D

Evaluation of Genotype-Based Gene Expression Model Performance: A Cross-Framework and Cross-Dataset Study

Genes 2021; 12(10):1531.

Yang F, Gleason KJ, Wang J, Duan J, He X, Pierce BL, Chen LS

CCmed: cross-condition mediation analysis for identifying replicable trans-associations mediated by cis-gene expression

Bioinformatics 2021; 37(17):2513-2520.

Abel ME, Zhang X, Asah SM, Wolfinger A, McCullumsmith RE, O'Donovan SM

KEOPS complex expression in the frontal cortex in major depression and schizophrenia

The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2020; 22(6):446-455.

Anderson KM, Collins MA, Chin R, Ge T, Rosenberg MD, Holmes AJ

Transcriptional and imaging-genetic association of cortical interneurons, brain function, and schizophrenia risk

Nature Communications 2020; 11:2889.

Dumitrescu L, Mahoney ER, Mukherjee S, Lee ML, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski C, Hernandez Saucedo H, Widaman KF, Buckley R, Properzi M, Mormino E, Yang HS, Harrison T, Hedden T, Nho K, Andrews SJ, Tommet D, Hadad N, Sanders RE, Ruderfer DM, Gifford KA, Moore AM, Cambronero F, Zhong X, Raghavan NS, Vardarajan B, Pericak-Vance MA, Farrer LA, Wang LS, Cruchaga C, Schellenberg G, Cox NJ, Haines JL, Keene CD, Saykin AJ, Larson EB, Sperling RA, Mayeux R, Bennett DA, Schneider JA, Crane PK, Jefferson AL, Hohman TJ

Genetic variants and functional pathways associated with resilience to Alzheimer's disease

Brain 2020; 143(8):2561-2575.

Folkersen L, Pain O, Ingason A, Werge T, Lewis CM, Austin J

Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores

Frontiers in Genetics 2020; 11:578.

Han L, Zhao X, Benton ML, Perumal T, Collins RL, Hoffman GE, Johnson JS, Sloofman L, Wang HZ, Stone MR, Brennand KJ, Brand H, Sieberts SK, Marenco S, Peters MA, Lipska BK, Roussos P, Capra JA, Talkowski M, Ruderfer DM

Functional annotation of rare structural variation in the human brain

Nature Communications 2020; 11:2990.

Li W, Cai X, Li HJ, Song M, Zhang CY, Yang Y, Zhang L, Zhao L, Liu W, Wang L, Shao M, Zhang Y, Zhang C, Cai J, Zhou DS, Li X, Hui L, Jia QF, Qu N, Zhong BL, Zhang SF, Chen J, Xia B, Li Y, Song X, Fan W, Tang W, Tang W, Tang J, Chen X, Yue W, Zhang D, Fang Y, Xiao X, Li M, Lv L, Chang H

Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder

Neuropsychopharmacology 2020; 46(6):1103-1112.

Li HJ, Qu N, Hui L, Cai X, Zhang CY, Zhong BL, Zhang SF, Chen J, Xia B, Wang L, Jia QF, Li W, Chang H, Xiao X, Li M, Li Y

Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data

Translational Psychiatry 2020; 10:98.

Lin CW, Chang LC, Ma T, Oh H, French B, Puralewski R, Mathews F, Fang Y, Lewis DA, Kennedy JL, Mueller D, Marshe VS, Jaffe A, Chen Q, Ursini G, Weinberger D, Newman AB, Lenze EJ, Nikolova YS, Tseng GC, Sibille E

Older Molecular Brain Age in Severe Mental Illness

Molecular psychiatry 2020; 26(7):3646-3656.

Liu W, Li W, Cai X, Yang Z, Li H, Su X, Song M, Zhou DS, Li X, Zhang C, Shao M, Zhang L, Yang Y, Zhang Y, Zhao J, Chang H, Yao YG, Fang Y, Lv L, Li M, Xiao X

Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci

Neuropsychopharmacology 2020; 45(7):1196-1206.

Bowen EF, Burgess JL, Granger R, Kleinman JE, Rhodes CH

DLPFC transcriptome defines two molecular subtypes of schizophrenia

Translational Psychiatry 2019; 9:147.

Breen MS, Dobbyn A, Li Q, Roussos P, Hoffman GE, Stahl E, Chess A, Sklar P, Li JB, Devlin B, Buxbaum JD

Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia

Nature neuroscience 2019; 22(9):1402-1412.

Gamazon ER, Zwinderman AH, Cox NJ, Denys D, Derks EM

Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits

Nature genetics 2019; 51(6):933-940.

Hoffman GE, Bendl J, Voloudakis G, Montgomery KS, Sloofman L, Wang YC, Shah HR, Hauberg ME, Johnson JS, Girdhar K, Song L, Fullard JF, Kramer R, Hahn CG, Gur R, Marenco S, Lipska BK, Lewis DA, Haroutunian V, Hemby S, Sullivan P, Akbarian S, Chess A, Buxbaum JD, Crawford GE, Domenici E, Devlin B, Sieberts SK, Peters MA, Roussos P

CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder

Scientific Data 2019; 6:180.

Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, Gamazon ER, Purcell S, Demontis D, Børglum AD, Walters JT, O'Donovan MC, Sullivan P, Owen MJ, Devlin B, Sieberts SK, Cox NJ, Im HK, Sklar P, Stahl EA

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.

Nature genetics 2019; 51(4):659-674.

Huo Y, Li S, Liu J, Li X, Luo XJ

Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk

Nature Communications 2019; 10:670.

Li YI, Wong G, Humphrey J, Raj T

Prioritizing Parkinson's disease genes using population-scale transcriptomic data

Nature Communications 2019; 10:994.

Liu W, Yan H, Zhou D, Cai X, Zhang Y, Li S, Li H, Li S, Zhou DS, Li X, Zhang C, Sun Y, Dai JP, Zhong J, Yao YG, Luo XJ, Fang Y, Zhang D, Ma Y, Yue W, Li M, Xiao X

The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population

Translational Psychiatry 2019; 9:333.

Niu HM, Yang P, Chen HH, Hao RH, Dong SS, Yao S, Chen XF, Yan H, Zhang YJ, Chen YX, Jiang F, Yang TL, Guo Y

Comprehensive functional annotation of susceptibility SNPs prioritized 10 genes for schizophrenia

Translational Psychiatry 2019; 9:56.

Seney ML, Cahill K, Enwright JF III, Logan RW, Huo Z, Zong W, Tseng G, McClung CA

Diurnal rhythms in gene expression in the prefrontal cortex in schizophrenia

Nature Communications 2019; 10:3355.

Vawter MP, Schulmann A, Alhassen L, Alhassen W, Hamzeh AR, Sakr J, Pauluk L, Yoshimura R, Wang X, Dai Q, Sanathara N, Civelli O, Alachkar A

Melanin Concentrating Hormone Signaling Deficits in Schizophrenia: Association With Memory and Social Impairments and Abnormal Sensorimotor Gating

International Journal of Neuropsychopharmacology 2019; 23(1):53-65.

Ward J, Tunbridge EM, Sandor C, Lyall LM, Ferguson A, Strawbridge RJ, Lyall DM, Cullen B, Graham N, Johnston KJ, Webber C, Escott-Price V, O'Donovan M, Pell JP, Bailey ME, Harrison PJ, Smith DJ

The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

Molecular psychiatry 2019; 25(11):3091-3099.

Wu Y, Bi R, Zeng C, Ma C, Sun C, Li J, Xiao X, Li M, Zhang DF, Zheng P, Sheng N, Luo XJ, Yao YG

Identification of the primate-specific gene BTN3A2 as an additional schizophrenia risk gene in the MHC loci

EBioMedicine 2019; 44:530-541.

Zullo JM, Drake D, Aron L, O'Hern P, Dhamne SC, Davidsohn N, Mao CA, Klein WH, Rotenberg A, Bennett DA, Church GM, Colaiácovo MP, Yankner BA

Regulation of Lifespan by Neural Excitation and REST

Nature 2019; 574(7778):359-364.

Amiri A, Coppola G, Scuderi S, Wu F, Roychowdhury T, Liu F, Pochareddy S, Shin Y, Safi A, Song L, Zhu Y, Sousa AM, Gerstein M, Crawford GE, Sestan N, Abyzov A, Vaccarino FM

Transcriptome and epigenome landscape of human cortical development modeled in brain organoids

Science (New York, N.Y.) 2018; 362(6420):eaat6720.

Bettella F, Brown AA, Smeland OB, Wang Y, Witoelar A, Buil Demur AA, Thompson WK, Zuber V, Dale AM, Djurovic S, Andreassen OA

Cross-tissue eQTL enrichment of associations in schizophrenia

PLoS ONE 2018; 13(9):e0202812.

Bryois J, Garrett ME, Song L, Safi A, Giusti-Rodriguez P, Johnson GD, Shieh AW, Buil A, Fullard JF, Roussos P, Sklar P, Akbarian S, Haroutunian V, Stockmeier CA, Wray GA, White KP, Liu C, Reddy TE, Ashley-Koch A, Sullivan PF, Crawford GE

Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

Nature Communications 2018; 9:3121.

de Sena Cortabitarte A, Berkel S, Cristian FB, Fischer C, Rappold GA

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders

Journal of Neurodevelopmental Disorders 2018; 10:15.

Dobbyn A, Huckins LM, Boocock J, Sloofman LG, Glicksberg BS, Giambartolomei C, Hoffman GE, Perumal TM, Girdhar K, Jiang Y, Raj T, Ruderfer DM, Kramer RS, Pinto D, Akbarian S, Roussos P, Domenici E, Devlin B, Sklar P, Stahl EA, Sieberts SK

Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS

American Journal of Human Genetics 2018; 102(6):1169-1184.

Fazio L, Pergola G, Papalino M, Di Carlo P, Monda A, Gelao B, Amoroso N, Tangaro S, Rampino A, Popolizio T, Bertolino A, Blasi G

Transcriptomic context of DRD1 is associated with prefrontal activity and behavior during working memory

Proceedings of the National Academy of Sciences of the United States of America 2018; 115(21):5582-5587.

Gandal MJ, Zhang P, Hadjimichael E, Walker RL, Chen C, Liu S, Won H, van Bakel H, Varghese M, Wang Y, Shieh AW, Haney J, Parhami S, Belmont J, Kim M, Losada PM, Khan Z, Mleczko J, Xia Y, Dai R, Wang D, Yang YT, Xu M, Fish K, Hof PR, Warrell J, Fitzgerald D, White K, Jaffe AE, Peters MA, Gerstein M, Liu C, Iakoucheva LM, Pinto D, Geschwind DH

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Science (New York, N.Y.) 2018; 362(6420):eaat8127.

Gandal MJ, Haney JR, Parikshak NN, Leppa V, Ramaswami G, Hartl C, Schork AJ, Appadurai V, Buil A, Werge TM, Liu C, White KP, Horvath S, Geschwind DH

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

Science (New York, N.Y.) 2018; 359(6376):693-697.

Giambartolomei C, Zhenli Liu J, Zhang W, Hauberg M, Shi H, Boocock J, Pickrell J, Jaffe AE, Pasaniuc B, Roussos P

A Bayesian framework for multiple trait colocalization from summary association statistics

Bioinformatics 2018; 34(15):2538-2545.

Girdhar K, Hoffman GE, Jiang Y, Brown L, Kundakovic M, Hauberg ME, Francoeur NJ, Wang YC, Shah H, Kavanagh DH, Zharovsky E, Jacobov R, Wiseman JR, Park R, Johnson JS, Kassim BS, Sloofman L, Mattei E, Weng Z, Sieberts SK, Peters MA, Harris BT, Lipska BK, Sklar P, Roussos P, Akbarian S

Cell-specific histone modification maps link schizophrenia risk to the neuronal epigenome

Nature neuroscience 2018; 21(8):1126-1136.

Gulyás-Kovács A, Keydar I, Xia E, Fromer M, Hoffman G, Ruderfer D, Sachidanandam R, Chess A

Unperturbed expression bias of imprinted genes in schizophrenia

Nature Communications 2018; 9:2914.

Gusev A, Mancuso N, Won H, Kousi M, Finucane HK, Reshef Y, Song L, Safi A, McCarroll S, Neale B, Ophoff RA, O'Donovan MC, Crawford GE, Geschwind DH, Katsanis N, Sullivan PF, Pasaniuc B, Price AL

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Nature genetics 2018; 50(4):538-548.

Hagenauer MH, Schulmann A, Li JZ, Vawter MP, Walsh DM, Thompson RC, Turner CA, Bunney WE, Myers RM, Barchas JD, Schatzberg AF, Watson SJ, Akil H

Inference of cell type content from human brain transcriptomic datasets illuminates the effects of age, manner of death, dissection, and psychiatric diagnosis

PLoS ONE 2018; 13(7):e0200003.

Hauberg ME, Fullard JF, Zhu L, Cohain A, Giambartolomei C, Misir R, Reach S, Johnson JS, Wang M, Mattheisen M, Børglum AD, Zhang B, Sieberts SK, Peters MA, Domenici E, Schadt EE, Devlin B, Sklar P, Roeder K, Roussos P

Differential Activity of Transcribed Enhancers in the Prefrontal Cortex of 537 cases with Schizophrenia and Controls

Molecular psychiatry 2018; 10.1038/s41380-018-0059-8.

Jaffe AE, Straub RE, Shin JH, Tao R, Gao Y, Collado-Torres L, Kam-Thong T, Xi HS, Quan J, Chen Q, Colantuoni C, Ulrich WS, Maher BJ, Deep-Soboslay A, Cross AJ, Brandon NJ, Leek JT, Hyde TM, Kleinman JE, Weinberger DR

Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis

Nature neuroscience 2018; 21(8):1117-1125.

Li M, Santpere G, Kawasawa YI, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, Choi J, Muchnik S, Xu X, Wang D, Lorente-Galdos B, Liu S, Giusti-Rodríguez P, Won H, de Leeuw CA, Pardiñas AF, Hu M, Jin F, Li Y, Owen MJ, O'Donovan MC, Walters JT, Posthuma D, Reimers MA, Levitt P, Weinberger DR, Hyde TM, Kleinman JE, Geschwind DH, Hawrylycz MJ, State MW, Sanders SJ, Sullivan PF, Gerstein MB, Lein ES, Knowles JA, Sestan N

Integrative functional genomic analysis of human brain development and neuropsychiatric risks

Science (New York, N.Y.) 2018; 362(6420):eaat7615.

Liu Y, Chang X, Hahn CG, Gur RE, Sleiman PA, Hakonarson H

Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease

Translational Psychiatry 2018; 8:44.

Mancuso N, Gayther S, Gusev A, Zheng W, Penney KL, Kote-Jarai Z, Eeles R, Freedman M, Haiman C, Pasaniuc B

Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

Nature Communications 2018; 9:4079.

Qi T, Wu Y, Zeng J, Zhang F, Xue A, Jiang L, Zhu Z, Kemper K, Yengo L, Zheng Z, Marioni RE, Montgomery GW, Deary IJ, Wray NR, Visscher PM, McRae AF, Yang J

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Nature Communications 2018; 9:2282.

Raj T, Li YI, Wong G, Humphrey J, Wang M, Ramdhani S, Wang YC, Ng B, Gupta I, Haroutunian V, Schadt EE, Young-Pearse T, Mostafavi S, Zhang B, Sklar P, Bennett DA, De Jager PL

Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility

Nature genetics 2018; 50(11):1584-1592.

Reay WR, Atkins JR, Quidé Y, Carr VJ, Green MJ, Cairns MJ

Polygenic disruption of retinoid signalling in schizophrenia and a severe cognitive deficit subtype

Molecular Psychiatry 2018; 25(4):719-731.

Toker L, Mancarci BO, Tripathy S, Pavlidis P

Transcriptomic evidence for alterations in astrocytes and parvalbumin interneurons in bipolar disorder and schizophrenia subjects

Biological psychiatry 2018; 84(11):787-796.

Wang D, Liu S, Warrell J, Won H, Shi X, Navarro FC, Clarke D, Gu M, Emani P, Yang YT, Xu M, Gandal MJ, Lou S, Zhang J, Park JJ, Yan C, Rhie SK, Manakongtreecheep K, Zhou H, Nathan A, Peters M, Mattei E, Fitzgerald D, Brunetti T, Moore J, Jiang Y, Girdhar K, Hoffman GE, Kalayci S, Gümüş ZH, Crawford GE, Roussos P, Akbarian S, Jaffe AE, White KP, Weng Z, Sestan N, Geschwind DH, Knowles JA, Gerstein MB

Comprehensive functional genomic resource and integrative model for the human brain

Science (New York, N.Y.) 2018; 362(6420):eaat8464.

Agrawal A, Chou YL, Carey CE, Baranger DA, Zhang B, Sherva R, Wetherill L, Kapoor M, Wang JC, Bertelsen S, Anokhin AP, Hesselbrock V, Kramer J, Lynskey MT, Meyers JL, Nurnberger JI, Rice JP, Tischfield J, Bierut LJ, Degenhardt L, Farrer LA, Gelernter J, Hariri AR, Heath AC, Kranzler HR, Madden PA, Martin NG, Montgomery GW, Porjesz B, Wang T, Whitfield JB, Edenberg HJ, Foroud T, Goate AM, Bogdan R, Nelson EC

Genomewide association study identifies a novel locus for cannabis dependence

Molecular psychiatry 2017; 23(5):1293-1302.

Hauberg ME, Zhang W, Giambartolomei C, Franzén O, Morris DL, Vyse TJ, Ruusalepp A, Sklar P, Schadt EE, Björkegren JL, Roussos P

Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression

American Journal of Human Genetics 2017; 100(6):885-894.

Jaffe AE, Tao R, Norris AL, Kealhofer M, Nellore A, Shin JH, Kim D, Jia Y, Hyde TM, Kleinman JE, Straub RE, Leek JT, Weinberger DR

qSVA framework for RNA quality correction in differential expression analysis

Proceedings of the National Academy of Sciences of the United States of America 2017; 114(27):7130-7135.

Jasinska AJ, Zelaya I, Service SK, Peterson CB, Cantor RM, Choi OW, DeYoung J, Eskin E, Fairbanks LA, Fears S, Furterer AE, Huang YS, Ramensky V, Schmitt CA, Svardal H, Jorgensen MJ, Kaplan JR, Villar D, Aken BL, Flicek P, Nag R, Wong ES, Blangero J, Dyer TD, Bogomolov M, Benjamini Y, Weinstock GM, Dewar K, Sabatti C, Wilson RK, Jentsch JD, Warren W, Coppola G, Woods RP, Freimer NB

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Nature genetics 2017; 49(12):1714-1721.

Lam M, Trampush JW, Yu J, Knowles E, Davies G, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, Lundervold AJ, Steen VM, Espeseth T, Räikkönen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Chiba-Falek O, Attix DK, Need AC, Cirulli ET, Voineskos AN, Stefanis NC, Avramopoulos D, Hatzimanolis A, Arking DE, Smyrnis N, Bilder RM, Freimer NA, Cannon TD, London E, Poldrack RA, Sabb FW, Congdon E, Conley ED, Scult MA, Dickinson D, Straub RE, Donohoe G, Morris D, Corvin A, Gill M, Hariri AR, Weinberger DR, Pendleton N, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK, Lencz T

Large-scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

Cell reports 2017; 21(9):2597-2613.

Mancuso N, Shi H, Goddard P, Kichaev G, Gusev A, Pasaniuc B

Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits

American Journal of Human Genetics 2017; 100(3):473-487.

Mitchell AC, Javidfar B, Pothula V, Ibi D, Shen EY, Peter CJ, Bicks L, Fehr T, Jiang Y, Brennand KJ, Neve RL, Gonzalez-Maeso J, Akbarian S

MEF2C TRANSCRIPTION FACTOR IS ASSOCIATED WITH THE GENETIC AND EPIGENETIC RISK ARCHITECTURE OF SCHIZOPHRENIA AND IMPROVES COGNITION IN MICE

Molecular psychiatry 2017; 23(1):123-132.

Zhu L, Lei J, Devlin B, Roeder K

TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES

The annals of applied statistics 2017; 11(3):1810-1831.

Chung DW, Volk DW, Arion D, Zhang Y, Sampson AR, Lewis DA

Dysregulated ErbB4 Splicing in Schizophrenia: Selective Effects on Parvalbumin Expression

The American journal of psychiatry 2015; 173(1):60-68.

Controls

Sanders AR, Beecham GW, Guo S, Dawood K, Rieger G, Badner JA, Gershon ES, Krishnappa RS, Kolundzija AB, Duan J, Gejman PV, Bailey JM, Martin ER

Genome-Wide Association Study of Male Sexual Orientation

Scientific Reports 2017; 7:16950.

Begum F, Chowdhury R, Cheung VG, Sherman SL, Feingold E

Genome-Wide Association Study of Meiotic Recombination Phenotypes

G3: Genes|Genomes|Genetics 2016; 6(12):3995-4007.

Pirooznia M, Wang T, Avramopoulos D, Potash J, Zandi P, Goes F

High-throughput sequencing of the synaptome in major depressive disorder

Molecular psychiatry 2015; 21(5):650-655.

CLARKE TK, WEISS AR, FERARRO TN, KAMPMAN KM, DACKIS CA, PETTINATI HM, O'BRIEN CP, OSLIN DW, LOHOFF FW, BERRETTINI WH

The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction

Annals of human genetics 2014; 78(1):33-39.

Johnson EO, Hancock DB, Levy JL, Gaddis NC, Saccone NL, Bierut LJ, Page GP

Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy

Human genetics 2013; 132(5):509-522.

Vijai J, Kirchhoff T, Schrader KA, Brown J, Dutra-Clarke AV, Manschreck C, Hansen N, Rau-Murthy R, Sarrel K, Przybylo J, Shah S, Cheguri S, Stadler Z, Zhang L, Paltiel O, Ben-Yehuda D, Viale A, Portlock C, Straus D, Lipkin SM, Lacher M, Robson M, Klein RJ, Zelenetz A, Offit K

Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies

PLoS Genetics 2013; 9(1):e1003220.

Chen J, Brunzell DH, Jackson K, van der Vaart A, Ma JZ, Payne TJ, Sherva R, Farrer LA, Gejman P, Levinson DF, Holmans P, Aggen SH, Damaj I, Kuo PH, Webb BT, Anton R, Kranzler HR, Gelernter J, Li MD, Kendler KS, Chen X

Correction: ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure

PLoS ONE 2012; 7(8):10.1371/annotation/071abcbd-6f0c-4c4b-9507-dae42450457e.

Clarke TK, Ambrose-Lanci L, Ferraro TN, Berrettini WH, Kampman KM, Dackis CA, Pettinati HM, O'Brien CP, Oslin DW, Lohoff FW

Genetic association analyses of PDYN polymorphisms with heroin and cocaine addiction

Genes, Brain and Behavior 2012; 11(4):415-423.

Priest JR, Girirajan S, Vu TH, Olson A, Eichler EE, Portman MA

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects

American Journal of Medical Genetics Part A 2012; 158(6):1279-1284.

Celestino-Soper PBS, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

Human molecular genetics 2011; 20(22):4360-4370.

Girirajan S, Brkanac Z, Coe BP, Baker C, Vives L, Vu TH, Shafer N, Bernier R, Ferrero GB, Silengo M, Warren ST, Moreno CS, Fichera M, Romano C, Raskind WH, Eichler EE

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

PLoS Genetics 2011; 7(11):e1002334.

Howrigan D, Laird N, Smoller J, Devlin B, McQueen M

Using Linkage Information to Weight a Genome-Wide Association of Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2011; 156(4):462-471.

Stewart LR, Hall AL, Kang SHL, Shaw CA, Beaudet AL

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

BMC medical genetics 2011; 12(1):154.

Goldstein BA, Hubbard AE, Cutler A, Barcellos LF

An application of Random Forests to a genome-wide association dataset: Methodological considerations & new findings

BMC Genetics 2010; 11:49.

Gyawali S, Subaran R, Weissman MM, Hershkowitz D, McKenna MC, Talati A, Fyer AJ, Wickramaratne P, Adams PB, Hodge SE

Association of a polyadenylation polymorphism in the serotonin transporter and panic disorder

Biological psychiatry 2010; 67(4):331-338.

Guan W, Liang L, Boehnke M, Abecasis GR

Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies

Genetic epidemiology 2009; 33(6):508-517.

McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O

Microduplications of 16p11. 2 are associated with schizophrenia

Nature genetics 2009; 41(11):1223-1227.

Evans LM, Akiskal HS, Greenwood TA, Nievergelt CM, Keck PD Jr, McElroy SL, Sadovnick AD, Remick RA, Schork NJ, Kelsoe JR

Suggestive linkage of a chromosomal locus on 18p11 to cyclothymic temperament in bipolar disorder families

Am J Med Genet Neuropsychiatr Genet 2008; 147(3):326-332.

Lekman M, Laje G, Charney D, Rush AJ, Wilson AF, Sorant AJ, Lipsky R, Wisniewski SR, Manji H, McMahon FJ, Paddock S

The FKBP5-gene in depression and treatment response - an association study in the STAR*D-cohort

Biological psychiatry 2008; 63(12):1103-1110.

Lohoff FW, Weller AE, Bloch PJ, Nall AH, Ferraro TN, Kampman KM, Pettinati HM, Oslin DW, Dackis CA, O'Brien CP

Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence

Neuropsychopharmacology 2008; 33(13):3078-3084.

Sklar P, Smoller J, Fan J, Ferreira M, Perlis R, Chambert K, Nimgaonkar V, McQueen M, Faraone S, Kirby A, de Bakker P, Ogdie M, Thase M, Sachs G, Todd-Brown K, Gabriel S, Sougnez C, Gates C, Blumenstiel B, Defelice M, Ardlie K, Franklin J, Muir W, McGhee K, MacIntyre D, McLean A, VanBeck M, McQuillin A, Bass N, Robinson M, Lawrence J, Anjorin A, Curtis D, Scolnick E, Daly M, Blackwood D, Gurling H, Purcell S

Whole-genome Association Study of Bipolar Disorder

Molecular psychiatry 2008; 13(6):558-569.

Hattori E, Liu C, Zhu H, Gershon ES

Genetic tests of biologic systems in affective disorders

Mol Psychiatry 2005; 10:719-740.

Nguyen TH, Liu C, Gershon ES, McMahon FJ

Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers

Bioinformatics 2004; 20:439-443.

Liu C, Bonner TI, Nguyen T, Lyons JL, Christian SL, Gershon ES

DNannotator: annotation software tool kit for regional genomic sequences

Nucleic Acids Res 2003; 31:3729-3735.

Stewart L, Hall AL, Kang SHL, Shaw CA, Beaudet AL

Supplemental Methods

Depression

Fanelli G, Sokolowski M, Wasserman D, Kasper S, Zohar J, Souery D, Montgomery S, Albani D, Forloni G, Ferentinos P, Rujescu D, Mendlewicz J, De Ronchi D, Serretti A, Fabbri C

Polygenic risk scores for neuropsychiatric, inflammatory, and cardio-metabolic traits highlight possible genetic overlap with suicide attempt and treatment-emergent suicidal ideation

American Journal of Medical Genetics 2022; 189(3-4):74-85.

Mason BL, Minhajuddin A, Czysz AH, Jha MK, Gadad BS, Mayes TL, Trivedi MH

Fibroblast growth factor 21 (FGF21) is increased in MDD and interacts with body mass index (BMI) to affect depression trajectory

Translational Psychiatry 2022; 12:16.

Magri C, Giacopuzzi E, Sacco C, Bocchio-Chiavetto L, Minelli A, Gennarelli M

Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles

Scientific Reports 2021; 11:727.

Fabbri Chiara, Kasper Siegfried, Kautzky Alexander, Zohar Joseph, Souery Daniel, Montgomery Stuart, Albani Diego, Forloni Gianluigi, Ferentinos Panagiotis, Rujescu Dan, Mendlewicz Julien, Uher Rudolf, Lewis Cathryn M, Serretti Alessandro

A polygenic predictor of treatment-resistant depression using whole exome sequencing and genome-wide genotyping.

Translational psychiatry 2020; 10(1):50.

Baez LM, Heller AS

Impact of age at onset on the phenomenology of depression in treatment-seeking adults in the STAR*D trial

Journal of affective disorders 2019; 262:381-388.

Coleman JR, Gaspar HA, Bryois J, Breen G

The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

Biological psychiatry 2019; 88(2):169-184.

Jha MK, Minhajuddin A, Chin-Fatt C, Greer T, Carmody T, Trivedi MH

Sex differences in the association of baseline c-reactive protein (CRP) and acute-phase treatment outcomes in major depressive disorder: Findings from the EMBARC study

Journal of psychiatric research 2019; 113:165-171.

Mullins N, Bigdeli TB, Børglum AD, Coleman JR, Demontis D, Fanous AH, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A, Corvin A, Sanders AR, Forstner AJ, Reif A, Koller AC, Świątkowska B, Baune BT, Müller-Myhsok B, Konte B, Penninx BW, Pato C, Zai C, Rujescu D, Hougaard DM, Quested D, Levinson DF, Binder EB, Byrne EM, Agerbo E, Streit F, Mayoral F, Bellivier F, Degenhardt F, Breen G, Morken G, Turecki G, Rouleau GA, Grabe HJ, Völzke H, Jones I, Giegling I, Agartz I, Melle I, Lawrence J, Potash JB, Walters JT, Strohmaier J, Shi J, Hauser J, Biernacka JM, Vincent JB, Kelsoe J, Strauss JS, Lissowska J, Pimm J, Smoller JW, Guzman Parra J, Berger K, Scott LJ, Jones LA, Azevedo MH, Trzaskowski M, Kogevinas M, Rietschel M, Boks M, Ising M, Grigoroiu-Serbanescu M, Hamshere ML, Leboyer M, Frye M, Nöthen MM, Alda M, Preisig M, Nordentoft M, Boehnke M, O'Donovan MC, Owen MJ, Pato MT, Renteria M, Budde M, Weissman MM, Wray NR, Bass N, Craddock N, Smeland OB, Andreassen OA, Mors O, Gejman PV, Sklar P, McGrath P, Hoffmann P, McGuffin P, Lee PH, Mortensen PB, Kahn RS, Ophoff RA, Adolfsson R, Van der Auwera S, Djurovic S, Shyn SI, Kloiber S, Heilmann-Heimbach S, Jamain S, Hamilton SP, McElroy SL, Lucae S, Cichon S, Schulze TG, Hansen T, Werge T, Air TM, Nimgaonkar V, Appadurai V, Cahn W, Milaneschi Y, Kendler KS, McQuillin A, Lewis CM

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

The American journal of psychiatry 2019; 176(8):651-660.

Zhang X, Abdellaoui A, Rucker J, de Jong S, Potash JB, Weissman MM, Shi J, Knowles JA, Pato C, Pato M, Sobell J, Smit JH, Hottenga JJ, de Geus EJ, Lewis CM, Buttenschøn HN, Craddock N, Jones I, Jones L, McGuffin P, Mors O, Owen MJ, Preisig M, Rietschel M, Rice JP, Rivera M, Uher R, Gejman PV, Sanders AR, Boomsma D, Penninx BW, Breen G, Levinson DF

Genome-wide burden of rare short deletions is enriched in Major Depressive Disorder in four cohorts

Biological psychiatry 2019; 85(12):1065-1073.

Furman JL, Soyombo A, Czysz AH, Jha MK, Carmody TJ, Mason BL, Scherer PE, Trivedi MH

Adiponectin Moderates Antidepressant Treatment Outcome in the Combining Medications to Enhance Depression Outcomes Randomized Clinical Trial

Personalized medicine in psychiatry 2018; 9-10:1-7.

Guintivano J, Krohn H, Lewis C, Byrne EM, Henders AK, Ploner A, Kirk K, Martin NG, Milgrom J, Wray NR, Sullivan PF, Meltzer-Brody S

PPD ACT: an app-based genetic study of postpartum depression

Translational Psychiatry 2018; 8:260.

Bigdeli T B, Ripke S, Peterson R E, Trzaskowski M, Bacanu S-A, Abdellaoui A, Andlauer T F M, Beekman A T F, Berger K, Blackwood D H R, Boomsma D I, Breen G, Buttenschøn H N, Byrne E M, Cichon S, Clarke T-K, Couvy-Duchesne B, Craddock N, de Geus E J C, Degenhardt F, Dunn E C, Edwards A C, Fanous A H, Forstner A J, Frank J, Gill M, Gordon S D, Grabe H J, Hamilton S P, Hardiman O, Hayward C, Heath A C, Henders A K, Herms S, Hickie I B, Hoffmann P, Homuth G, Hottenga J-J, Ising M, Jansen R, Kloiber S, Knowles J A, Lang M, Li Q S, Lucae S, MacIntyre D J, Madden P A F, Martin N G, McGrath P J, McGuffin P, McIntosh A M, Medland S E, Mehta D, Middeldorp C M, Milaneschi Y, Montgomery G W, Mors O, Müller-Myhsok B, Nauck M, Nyholt D R, Nöthen M M, Owen M J, Penninx B W J H, Pergadia M L, Perlis R H, Peyrot W J, Porteous D J, Potash J B, Rice J P, Rietschel M, Riley B P, Rivera M, Schoevers R, Schulze T G, Shi J, Shyn S I, Smit J H, Smoller J W, Streit F, Strohmaier J, Teumer A, Treutlein J, Van der Auwera S, van Grootheest G, van Hemert A M, Völzke H, Webb B T, Weissman M M, Wellmann J, Willemsen G, Witt S H, Levinson D F, Lewis C M, Wray N R, Flint J, Sullivan P F, Kendler K S

Genetic effects influencing risk for major depressive disorder in China and Europe.

Translational psychiatry 2017; 7(3):e1074.

Power Robert A, Tansey Katherine E, Buttenschøn Henriette Nørmølle, Cohen-Woods Sarah, Bigdeli Tim, Hall Lynsey S, Kutalik Zoltán, Lee S Hong, Ripke Stephan, Steinberg Stacy, Teumer Alexander, Viktorin Alexander, Wray Naomi R, Arolt Volker, Baune Bernard T, Boomsma Dorret I, Børglum Anders D, Byrne Enda M, Castelao Enrique, Craddock Nick, Craig Ian W, Dannlowski Udo, Deary Ian J, Degenhardt Franziska, Forstner Andreas J, Gordon Scott D, Grabe Hans J, Grove Jakob, Hamilton Steven P, Hayward Caroline, Heath Andrew C, Hocking Lynne J, Homuth Georg, Hottenga Jouke J, Kloiber Stefan, Krogh Jesper, Landén Mikael, Lang Maren, Levinson Douglas F, Lichtenstein Paul, Lucae Susanne, MacIntyre Donald J, Madden Pamela, Magnusson Patrik K E, Martin Nicholas G, McIntosh Andrew M, Middeldorp Christel M, Milaneschi Yuri, Montgomery Grant W, Mors Ole, Müller-Myhsok Bertram, Nyholt Dale R, Oskarsson Hogni, Owen Michael J, Padmanabhan Sandosh, Penninx Brenda W J H, Pergadia Michele L, Porteous David J, Potash James B, Preisig Martin, Rivera Margarita, Shi Jianxin, Shyn Stanley I, Sigurdsson Engilbert, Smit Johannes H, Smith Blair H, Stefansson Hreinn, Stefansson Kari, Strohmaier Jana, Sullivan Patrick F, Thomson Pippa, Thorgeirsson Thorgeir E, Van der Auwera Sandra, Weissman Myrna M, Breen Gerome, Lewis Cathryn M

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

Biological psychiatry 2017; 81(4):325-335.

Rivera M, Locke AE, Corre T, Czamara D, Wolf C, Ching-Lopez A, Milaneschi Y, Kloiber S, Cohen-Woods S, Rucker J, Aitchison KJ, Bergmann S, Boomsma DI, Craddock N, Gill M, Holsboer F, Hottenga JJ, Korszun A, Kutalik Z, Lucae S, Maier W, Mors O, Müller-Myhsok B, Owen MJ, Penninx BW, Preisig M, Rice J, Rietschel M, Tozzi F, Uher R, Vollenweider P, Waeber G, Willemsen G, Craig IW, Farmer AE, Lewis CM, Breen G, McGuffin P

Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals

The British Journal of Psychiatry 2017; 211(2):70-76.

Gill KE, Cardenas SA, Kassem L, Schulze TG, McMahon FJ

Symptom profiles and illness course among Anabaptist and Non-Anabaptist adults with major mood disorders

International Journal of Bipolar Disorders 2016; 4:21.

Osborne Lauren, Clive Makena, Kimmel Mary, Gispen Fiona, Guintivano Jerry, Brown Tori, Cox Olivia, Judy Jennifer, Meilman Samantha, Braier Aviva, Beckmann Matthias W, Kornhuber Johannes, Fasching Peter A, Goes Fernando, Payne Jennifer L, Binder Elisabeth B, Kaminsky Zachary

Replication of Epigenetic Postpartum Depression Biomarkers and Variation with Hormone Levels.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016; 41(6):1648-58.

Otowa T, Hek K, Lee M, Byrne EM, Mirza SS, Nivard MG, Bigdeli T, Aggen SH, Adkins D, Wolen A, Fanous A, Keller MC, Castelao E, Kutalik Z, Van der Auwera S, Homuth G, Nauck M, Teumer A, Milaneschi Y, Hottenga JJ, Direk N, Hofman A, Uitterlinden A, Mulder CL, Henders AK, Medland SE, Gordon S, Heath AC, Madden PA, Pergadia M, van der Most PJ, Nolte IM, van Oort FV, Hartman CA, Oldehinkel AJ, Preisig M, Grabe HJ, Middeldorp CM, Penninx BW, Boomsma D, Martin NG, Montgomery G, Maher BS, van den Oord EJ, Wray NR, Tiemeier H, Hettema JM

Meta-analysis of genome-wide association studies of anxiety disorders

Molecular psychiatry 2016; 10.1038/mp.2015.197.

Palmer RH, Beevers CG, McGeary JE, Brick LA, Knopik VS

A Preliminary Study of Genetic Variation in the Dopaminergic and Serotonergic Systems and Genome-wide Additive Genetic Effects on Depression Severity and Treatment Response

Clinical psychological science : a journal of the Association for Psychological Science 2016; 5(1):158-165.

GRAAE LISETTE, PADDOCK SILVIA, BELIN ANDREACARMINE

ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide

Genetics research 2015; 97:e8.

Knowles DA, Davis JR, Raj A, Zhu X, Potash JB, Weissman MM, Shi J, Levinson DF, Mostafavi S, Montgomery SB

Allele-specific expression reveals interactions between genetic variation and environment

bioRxiv 2015; 025874.

Leonpacher AK, Liebers D, Pirooznia M, Jancic D, MacKinnon DF, Mondimore FM, Schweizer B, Potash JB, Zandi PP, Goes FS

Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features

Psychological medicine 2015; 1-10.

Leonpacher AK, Liebers D, Pirooznia M, Jancic D, MacKinnon DF, Mondimore FM, Schweizer B, Potash JB, Zandi PP, Goes FS

Distinguishing bipolar from unipolar depression: the importance of clinical symptoms and illness features

Psychological medicine 2015; 45(11):2437-2446.

Minelli A, Magri C, Barbon A, Bonvicini C, Segala M, Congiu C, Bignotti S, Milanesi E, Trabucchi L, Cattane N

Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder

Translational Psychiatry 2015; 5(12):e687.

Osborne L, Clive M, Kimmel M, Gispen F, Guintivano J, Brown T, Cox O, Judy J, Meilman S, Braier A, Beckmann MW, Kornhuber J, Fasching PA, Goes F, Payne JL, Binder EB, Kaminsky Z

Replication of Epigenetic Postpartum Depression Biomarkers and Variation with Hormone Levels

Neuropsychopharmacology 2015; 41(6):1648-1658.

Peyrot W J, Lee S H, Milaneschi Y, Abdellaoui A, Byrne E M, Esko T, de Geus E J C, Hemani G, Hottenga J J, Kloiber S, Levinson D F, Lucae S, Martin N G, Medland S E, Metspalu A, Milani L, Noethen M M, Potash J B, Rietschel M, Rietveld C A, Ripke S, Shi J, Willemsen G, Zhu Z, Boomsma D I, Wray N R, Penninx B W J H

The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects.

Molecular psychiatry 2015; 20(6):735-43.

Yeh FC, Kao CF, Kuo PH

Explore the Features of Brain-Derived Neurotrophic Factor in Mood Disorders

PLoS ONE 2015; 10(6):e0128605.

Arias B, Fabbri C, Serretti A, Drago A, Mitjans M, Gastó C, Catalán R, Fañanás L

DISC1-TSNAX and DAOA genes in major depression and citalopram efficacy

Journal of affective disorders 2014; 168:91-97.

Davies MN, Krause L, Bell JT, Gao F, Ward KJ, Wu H, Lu H, Liu Y, Tsai PC, Collier DA, Murphy T, Dempster E, Mill J, Battle A, Mostafavi S, Zhu X, Henders A, Byrne E, Wray NR, Martin NG, Spector TD, Wang J

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

Genome Biology 2014; 15(4):R56.

Fabbri C, Marsano A, Albani D, Chierchia A, Calati R, Drago A, Crisafulli C, Calabrò M, Kasper S, Lanzenberger R, Zohar J, Juven-Wetzler A, Souery D, Montgomery S, Mendlewicz J, Serretti A

PPP3CC gene: a putative modulator of antidepressant response through the B-cell receptor signaling pathway.

Pharmacogenomics J 2014; 14(5):463-472.

Mostafavi S, Battle A, Zhu X, Potash J B, Weissman M M, Shi J, Beckman K, Haudenschild C, McCormick C, Mei R, Gameroff M J, Gindes H, Adams P, Goes F S, Mondimore F M, MacKinnon D F, Notes L, Schweizer B, Furman D, Montgomery S B, Urban A E, Koller D, Levinson D F

Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing.

Molecular psychiatry 2014; 19(12):1267-74.

Power Robert A, Keller Matthew C, Ripke Stephan, Abdellaoui Abdel, Wray Naomi R, Sullivan Patrick F, Breen Gerome

A recessive genetic model and runs of homozygosity in major depressive disorder.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014; 165B(2):157-66.

Chang SH, Gao L, Li Z, Zhang WN, Du Y, Wang J

BDgene: a genetic database for bipolar disorder and its overlap with schizophrenia and major depressive disorder

Biological psychiatry 2013; 74(10):727-733.

Fabbri C, Drago A, Serretti A

Early antidepressant efficacy modulation by glutamatergic gene variants in the STAR*D

Eur Neuropsychopharmacol 2013; 23(7):612-621.

GENDEP Investigators, MARS Investigators, STAR* D Investigators

Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies

American Journal of Psychiatry 2013

Hunter Aimee M, Leuchter Andrew F, Power Robert A, Muthén Bengt, McGrath Patrick J, Lewis Cathryn M, Cook Ian A, Garriock Holly A, McGuffin Peter, Uher Rudolf, Hamilton Steven P

A genome-wide association study of a sustained pattern of antidepressant response.

Journal of psychiatric research 2013; 47(9):1157-65.

Hunter AM, Leuchter AF, Power R, Muthén B, McGrath PJ, Lewis CM, Cook IA, Garriock HA, McGuffin P, Uher R, Hamilton SP

A Genome-wide Association Study of a Sustained Pattern of Antidepressant Response

Journal of psychiatric research 2013; 47(9):1157-1165.

Kripke DF, Nievergelt CM, Tranah GJ, Murray SS, Rex KM, Grizas AP, Hahn EK, Lee H-J, Kelsoe JR, Kline LE

FMR1, circadian genes and depression: suggestive associations or false discovery?

J Circadian Rhythms 2013; 11(1):3.

Mostafavi S, Battle A, Zhu X, Potash JB, Weissman MM, Shi J, Beckman K, Haudenschild C, McCormick C, Mei R

Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing

Molecular psychiatry 2013

Smith RM, Papp AC, Webb A, Ruble CL, Munsie LM, Nisenbaum LK, Kleinman JE, Lipska BK, Sadee W

Multiple regulatory variants modulate expression of 5-hydroxytryptamine 2A receptors in human cortex

Biol Psychiatry 2013; 73(6):546-554.

Stange JP, Sylvia LG, da Silva Magalhães PV, Miklowitz DJ, Otto MW, Frank E, Berk M, Nierenberg AA, Deckersbach T

Extreme Attributions Predict the Course of Bipolar Depression: Results from the STEP-BD Randomized Controlled Trial of Psychosocial Treatment

The Journal of clinical psychiatry 2013; 74(3):249-255.

Adkins D E, Clark S L, Åberg K, Hettema J M, Bukszár J, McClay J L, Souza R P, van den Oord E J C G

Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.

Translational psychiatry 2012; 2:e129.

Goes FS, McCusker MG, Bienvenu OJ, MacKinnon DF, Mondimore FM, Schweizer B, DePaulo JR Jr, Potash JB

Co-morbid anxiety disorders in bipolar disorder and major depression : familial aggregation and clinical characteristics of co-morbid panic disorder, social phobia, specific phobia and obsessive-compulsive disorder

Psychological medicine 2012; 42(7):1449-1459.

Judy JT, Seifuddin F, Mahon PB, Huo Y, Goes FS, Jancic D, Schweizer B, Mondimore FM, MacKinnon DF, DePaulo JR Jr, Gershon ES, McMahon FJ, Cutler DJ, Zandi PP, Potash JB, Willour VL

Association Study of Serotonin Pathway Genes in Attempted Suicide

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2012; 0(1):112-119.

Kloiber S, Ripke S, Kohli MA, Reppermund S, Salyakina D, Uher R, McGuffin P, Perlis RH, Hamilton SP, Pütz B, Hennings J, Brückl T, Klengel T, Bettecken T, Ising M, Uhr M, Dose T, Unschuld PG, Zihl J, Binder E, Müller-Myhsok B, Holsboer F, Lucae S

Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels

European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2012; 23(7):653-662.

Lee PH, Perlis RH, Jung JY, Byrne EM, Rueckert E, Siburian R, Haddad S, Mayerfeld CE, Heath AC, Pergadia ML, Madden PA, Boomsma DI, Penninx BW, Sklar P, Martin NG, Wray NR, Purcell SM, Smoller JW

Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder

Translational Psychiatry 2012; 2(11):e184.

Saunders EF, Fitzgerald KD, Zhang P, McInnis MG

CLINICAL FEATURES OF BIPOLAR DISORDER COMORBID WITH ANXIETY DISORDERS DIFFER BETWEEN MEN AND WOMEN

Depression and anxiety 2012; 29(8):739-746.

Uher R, Perlis RH, Placentino A, Dernovšek MZ, Henigsberg N, Mors O, Maier W, McGuffin P, Farmer A

SELF-REPORT AND CLINICIAN-RATED MEASURES OF DEPRESSION SEVERITY: CAN ONE REPLACE THE OTHER?

Depression and anxiety 2012; 29(12):1043-1049.

Alemi F, Zargoush M, Erdman H, Vang J, Epstein S, Ayman F

Genetic markers anticipate response to citalopram in a majority of patients

Psychiatr Genet 2011; 21(6):287-293.

Shyn S, Shi J, Kraft J, Potash J, Knowles J, Weissman M, Garriock H, Yokoyama J, McGrath P, Peters E, Scheftner W, Coryell W, Lawson W, Jancic D, Gejman P, Sanders A, Holmans P, Slager S, Levinson D, Hamilton S

Novel loci for major depression identified by genome-wide association study of STAR*D and meta-analysis of three studies

Molecular psychiatry 2011; 16(2):202-215.

Garriock HA, Tanowitz M, Kraft JB, Dang VC, Peters EJ, Jenkins GD, Reinalda MS, McGrath PJ, von Zastrow M, Slager SL, Hamilton SP

Association of mu-opioid receptor variants and response to citalopram treatment in major depressive disorder

Am J Psychiaty 2010; 167(5):565-573.

Garriock HA, Kraft JB, Shyn SI, Peters EJ, Yokoyama JS, Jenkins GD, Reinalda MS, Slager SL, McGrath PJ, Hamilton SP

A genomewide association study of citalopram response in major depressive disorder.

Biol Psychiatry 2010; 67(2):133-138.

Glessner JT, Wang K, Sleiman PM, Zhang H, Kim CE, Flory JH, Bradfield JP, Imielinski M, Frackelton EC, Qiu H, Mentch F, Grant SF, Hakonarson H

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

PLoS ONE 2010; 5(12):e15463.

Huang J, Perlis RH, Lee PH, Rush AJ, Fava M, Sachs GS, Lieberman J, Hamilton SP, Sullivan P, Sklar P, Purcell S, Smoller JW

Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression

The American journal of psychiatry 2010; 167(10):10.1176/appi.ajp.2010.09091335.

McClay JL, Adkins DE, Åberg K, Bukszár J, Khachane AN, Keefe RS, Perkins DO, McEvoy JP, Stroup TS, Vann RE, Beardsley PM, Lieberman JA, Sullivan PF, van den Oord EJ

Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia

Neuropsychopharmacology 2010; 36(3):616-626.

McMahon FJ, Akula N, Schulze TG, Muglia P, Tozzi F, Detera-Wadleigh SD, Steele CJ, Breuer R, Strohmaier J, Wendland JR, Mattheisen M, Mühleisen TW, Maier W, Nöthen MM, Cichon S, Farmer A, Vincent JB, Holsboer F, Preisig M, Rietschel M

Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1

Nature genetics 2010; 42(2):128-131.

Perlis RH, Smoller JW, Mysore J, Sun M, Gillis T, Purcell S, Rietschel M, Nöthen MM, Witt S, Maier W, Iosifescu DV, Sullivan P, Rush AJ, Fava M, Breiter H, Macdonald M, Gusella J

Prevalence of Incompletely Penetrant Huntington's Disease Alleles Among Individuals With Major Depressive Disorder

The American journal of psychiatry 2010; 167(5):574-579.

Ising Marcus, Lucae Susanne, Binder Elisabeth B, Bettecken Thomas, Uhr Manfred, Ripke Stephan, Kohli Martin A, Hennings Johannes M, Horstmann Sonja, Kloiber Stefan, Menke Andreas, Bondy Brigitta, Rupprecht Rainer, Domschke Katharina, Baune Bernhard T, Arolt Volker, Rush A John, Holsboer Florian, Müller-Myhsok Bertram

A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression.

Archives of general psychiatry 2009; 66(9):966-975.

Laje Gonzalo, Allen Andrew S, Akula Nirmala, Manji Husseini, John Rush A, McMahon Francis J

Genome-wide association study of suicidal ideation emerging during citalopram treatment of depressed outpatients.

Pharmacogenetics and genomics 2009; 19(9):666-74.

Mrazek D A, Rush A J, Biernacka J M, O'Kane D J, Cunningham J M, Wieben E D, Schaid D J, Drews M S, Courson V L, Snyder K A, Black J L, Weinshilboum R M

SLC6A4 variation and citalopram response.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009; 150B(3):341-51.

Payne JL, Klein SR, Zamoiski RB, Zandi PP, Bienvenu OJ, MacKinnon DF, Mondimore FM, Schweizer B, Swartz KL, Crowe RP, Scheftner WA, Weissman MM, Levinson DF, DePaulo JR Jr, Potash JB

Premenstrual mood symptoms: study of familiality and personality correlates in mood disorder pedigrees

Archives of women's mental health 2009; 12(1):10.1007/s00737-008-0043-4.

Peters EJ, Slager SL, Jenkins GD, Reinalda MS, Garriock HA, Shyn SI, Kraft JB, McGrath PJ, Hamilton SP

Resequencing of serotonin-related genes and association of tagging SNPs to citalopram response

Pharmacogenetics and genomics 2009; 19(1):1.

Crowley JJ, Keefe RS, Perkins DO, Stroup TS, Lieberman JA, Sullivan PF

The Neuregulin 1 Promoter Polymorphism rs6994992 is Not Associated with Chronic Schizophrenia or Neurocognition

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008; 0(7):10.1002/ajmg.b.30727.

Goes FS, Sadler B, Toolan J, Zamoiski RD, Mondimore FM, MacKinnon DF, Schweizer B, Raymond DePaulo J, Potash JB

Psychotic features in bipolar and unipolar depression

Bipolar disorders 2007; 9(8):901-906.

Holmans P, Weissman MM, Zubenko GS, Scheftner WA, Crowe RR, DePaulo JR, Knowles JA, Zubenko WN, Murphy-Eberenz K, Marta DH, Boutelle S, McInnis MG, Adams P, Gladis M, Steele J, Miller EB, Potash JB, MacKinnon DF, Levinson DF

Genetics of recurrent early-onset major depression (GenRED): Final genome scan report

Am J Psychiatry 2007; 164:248-258.

Levinson DF, Evgrafov OV, Knowles JA, Potash JB, Weissman MM, Scheftner WA, DePaulo JR, Crowe RR, Murphy-Eberenz K, Marta DH, McInnis MG, Adams P, Gladis M, Miller EB, Thomas J, Holmans P

Genetics of recurrent early-onset major depression (GenRED): Significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers

Am J Psychiatry 2007; 164:259-264.

Paddock S, Laje G, Charney D, A John Rush MD, Wilson AF, Sorant AJM, Lipsky R, Wisniewski SR, Manji H, McMahon FJ

Association of GRIK4 with outcome of antidepressant treatment in the STAR* D cohort

The American journal of psychiatry 2007; 164(8):1181-1188.

Payne JL, Roy PS, Murphy-Eberenz K, Weismann MM, Swartz KL, McInnis MG, Nwulia E, Mondimore FM, MacKinnon DF, Miller EB

Reproductive cycle-associated mood symptoms in women with major depression and bipolar disorder

Journal of affective disorders 2007; 99(1):221-229.

Verma R, Cutler DJ, Holmans P, Knowles JA, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR, Levinson DF, Potash JB

Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(8):1079-1082.

McMahon Francis J, Buervenich Silvia, Charney Dennis, Lipsky Robert, Rush A John, Wilson Alexander F, Sorant Alexa J M, Papanicolaou George J, Laje Gonzalo, Fava Maurizio, Trivedi Madhukar H, Wisniewski Stephen R, Manji Husseini

Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatment.

American journal of human genetics 2006; 78(5):804-814.

Mondimore FM, Zandi PP, MacKinnon DF, McInnis MG, Miller EB, Crowe RP, Scheftner WA, Marta DH, Weissman MM, Levinson DF, Murphy-Ebenez KP, DePaulo JR, Potash JB

Familial aggregation of illness chronocity in recurrent, early-onset major depression pedigrees

Am J Psychiatry 2006; 163:1554-1560.

Murphy-Eberenz K, Zandi PP, March D, Crowe RR, Scheftner WA, Alexander M, McInnis MG, Coryell W, Adams P, DePaulo JR, Miller EB, Marta DH, Potash JB, Payne J, Levinson DF

Is perinatal depression familial?

J Affective Disord 2006; 90(49-55):.

Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

Proceedings of the National Academy of Sciences of the United States of America 2005; 102(32):11545-11550.

Holmans Peter, Zubenko George S, Crowe Raymond R, DePaulo J Raymond, Scheftner William A, Weissman Myrna M, Zubenko Wendy N, Boutelle Sandra, Murphy-Eberenz Kathleen, MacKinnon Dean, McInnis Melvin G, Marta Diana H, Adams Philip, Knowles James A, Gladis Madeleine, Thomas Jo, Chellis Jennifer, Miller Erin, Levinson Douglas F

Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q.

American journal of human genetics 2004; 74(6):1154-67.

iPSC

Dobrindt K, Hoagland DA, Seah C, Kassim B, O'Shea CP, Murphy A, Iskhakova M, Fernando MB, Powell SK, Deans PJ, Javidfar B, Peter C, Møller R, Uhl SA, Garcia MF, Kimura M, Iwasawa K, Crary JF, Kotton DN, Takebe T, Huckins LM, tenOever BR, Akbarian S, Brennand KJ

Common Genetic Variation in Humans Impacts In Vitro Susceptibility to SARS-CoV-2 Infection

Stem Cell Reports 2021; 16(3):505-518.

Lizarraga SB, Ma L, Maguire AM, van Dyck LI, Wu Q, Ouyang Q, Kavanaugh BC, Nagda D, Livi LL, Pescosolido MF, Schmidt M, Alabi S, Cowen MH, Brito-Vargas P, Hoffman-Kim D, Uzun ED, Schlessinger A, Jones RN, Morrow EM

Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies

Science translational medicine 2021; 13(580):eaaw0682.

Dobrindt K, Hoagland DA, Seah C, Kassim B, O'Shea CP, Iskhakova M, Fernando MB, Deans PJ, Powell SK, Javidfar B, Murphy A, Peter C, Møeller R, Garcia MF, Kimura M, Iwasawa K, Crary J, Kotton DN, Takebe T, Huckins LM, tenOever BR, Akbarian S, Brennand KJ

Common genetic variation in humans impacts in vitro susceptibility to SARS-CoV-2 infection

bioRxiv 2020; 2020.09.20.300574.

Readhead Benjamin, Hartley Brigham J, Eastwood Brian J, Collier David A, Evans David, Farias Richard, He Ching, Hoffman Gabriel, Sklar Pamela, Dudley Joel T, Schadt Eric E, Savić Radoslav, Brennand Kristen J

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia.

Nature communications 2018; 9(1):4412.

Xu J, Hartley B J, Kurup P, Phillips A, Topol A, Xu M, Ononenyi C, Foscue E, Ho S-M, Baguley T D, Carty N, Barros C S, Müller U, Gupta S, Gochman P, Rapoport J, Ellman J A, Pittenger C, Aronow B, Nairn A C, Nestor M W, Lombroso P J, Brennand K J

null

Molecular psychiatry 2018; 23(2):271-281.

Boland Michael J, Nazor Kristopher L, Tran Ha T, Szücs Attila, Lynch Candace L, Paredes Ryder, Tassone Flora, Sanna Pietro Paolo, Hagerman Randi J, Loring Jeanne F

Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome.

Brain : a journal of neurology 2017; 140(3):582-598.

Dimitrion Peter, Zhi Yun, Clayton Dennis, Apodaca Gerard L, Wilcox Madeleine R, Johnson Jon W, Nimgaonkar Vishwajit, D'Aiuto Leonardo

Low-Density Neuronal Cultures from Human Induced Pluripotent Stem Cells.

Molecular neuropsychiatry 2017; 3(1):28-36.

Flaherty Erin, Deranieh Rania M, Artimovich Elena, Lee Inkyu S, Siegel Arthur J, Levy Deborah L, Nestor Michael W, Brennand Kristen J

Patient-derived hiPSC neurons with heterozygous CNTNAP2 deletions display altered neuronal gene expression and network activity.

NPJ schizophrenia 2017; 3(1):35.

Yang Nan, Chanda Soham, Marro Samuele, Ng Yi-Han, Janas Justyna A, Haag Daniel, Ang Cheen Euong, Tang Yunshuo, Flores Quetzal, Mall Moritz, Wapinski Orly, Li Mavis, Ahlenius Henrik, Rubenstein John L, Chang Howard Y, Buylla Arturo Alvarez, Südhof Thomas C, Wernig Marius

Generation of pure GABAergic neurons by transcription factor programming.

Nature methods 2017; 14(6):621-628.

Topol Aaron, Zhu Shijia, Hartley Brigham J, English Jane, Hauberg Mads E, Tran Ngoc, Rittenhouse Chelsea Ann, Simone Anthony, Ruderfer Douglas M, Johnson Jessica, Readhead Ben, Hadas Yoav, Gochman Peter A, Wang Ying-Chih, Shah Hardik, Cagney Gerard, Rapoport Judith, Gage Fred H, Dudley Joel T, Sklar Pamela, Mattheisen Manuel, Cotter David, Fang Gang, Brennand Kristen J

Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells.

Cell reports 2016; 15(5):1024-1036.

D'Aiuto L, Zhi Y, Kumar Das D, Wilcox MR, Johnson JW, McClain L, MacDonald ML, Di Maio R, Schurdak ME, Piazza P, Viggiano L, Sweet R, Kinchington PR, Bhattacharjee AG, Yolken R, Nimgaonka VL

Large-scale generation of human iPSC-derived neural stem cells/early neural progenitor cells and their neuronal differentiation

Organogenesis 2015; 10(4):365-377.

Lee IS, Carvalho CM, Douvaras P, Ho SM, Hartley BJ, Zuccherato LW, Ladran IG, Siegel AJ, McCarthy S, Malhotra D, Sebat J, Rapoport J, Fossati V, Lupski JR, Levy DL, Brennand KJ

Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells

NPJ Schizophrenia 2015; 1:15019-.

Lee Inkyu S, Carvalho Claudia M B, Douvaras Panagiotis, Ho Seok-Man, Hartley Brigham J, Zuccherato Luciana W, Ladran Ian G, Siegel Arthur J, McCarthy Shane, Malhotra Dheeraj, Sebat Jonathan, Rapoport Judith, Fossati Valentina, Lupski James R, Levy Deborah L, Brennand Kristen J

null

NPJ schizophrenia 2015; 1:.

D'Aiuto Leonardo, Zhi Yun, Kumar Das Dhanjit, Wilcox Madeleine R, Johnson Jon W, McClain Lora, MacDonald Matthew L, Di Maio Roberto, Schurdak Mark E, Piazza Paolo, Viggiano Luigi, Sweet Robert, Kinchington Paul R, Bhattacharjee Ayantika G, Yolken Robert, Nimgaonka Vishwajit L, Nimgaonkar Vishwajit L

Large-scale generation of human iPSC-derived neural stem cells/early neural progenitor cells and their neuronal differentiation.

Organogenesis 2014; 10(4):365-77.

Wang Y, Dolmetsch R

In vitro human corticogenesis

Neuron 2013; 77(3):379-381.

Dolmetsch R, Geschwind DH

The human brain in a dish: the promise of iPSC-derived neurons

Cell 2011; 145(6):831-834.

Pasca SP, Portmann T, Voineagu I, Yazawa M, Shcheglovitov A, Pasca AM, Cord B, Palmer TD, Chikahisa S, Nishino S, Bernstein JA, Hallmayer J, Geschwind DH, Dolmetsch RE

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome

Nat Med 2011; 17(12):1657-1662.

Yazawa M, Hsueh B, Jia X, Pasca AM, Bernstein JA, Hallmayer J, Dolmetsch RE

Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

Nature 2011; 471(7337):230-234.

Netherlands Twin Register

Mancuso N, Shi H, Goddard P, Kichaev G, Gusev A, Pasaniuc B

Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits

American Journal of Human Genetics 2017; 100(3):473-487.

Rivera M, Locke AE, Corre T, Czamara D, Wolf C, Ching-Lopez A, Milaneschi Y, Kloiber S, Cohen-Woods S, Rucker J, Aitchison KJ, Bergmann S, Boomsma DI, Craddock N, Gill M, Holsboer F, Hottenga JJ, Korszun A, Kutalik Z, Lucae S, Maier W, Mors O, Müller-Myhsok B, Owen MJ, Penninx BW, Preisig M, Rice J, Rietschel M, Tozzi F, Uher R, Vollenweider P, Waeber G, Willemsen G, Craig IW, Farmer AE, Lewis CM, Breen G, McGuffin P

Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals

The British Journal of Psychiatry 2017; 211(2):70-76.

Chen TH, Sun W, Fine JP

Designing penalty functions in high dimensional problems: The role of tuning parameters

Electronic journal of statistics 2016; 10(2):2312-2328.

Hillger JM, Schoop J, Boomsma DI, Slagboom PE, IJzerman AP, Heitman LH

Whole-cell biosensor for label-free detection of GPCR-mediated drug responses in personal cell lines

Biosensors and Bioelectronics 2015; 74:233-242.

Jelenkovic Aline, Yokoyama Yoshie, Sund Reijo, Honda Chika, Bogl Leonie H, Aaltonen Sari, Ji Fuling, Ning Feng, Pang Zengchang, Ordoñana Juan R, Sánchez-Romera Juan F, Colodro-Conde Lucia, Burt S Alexandra, Klump Kelly L, Medland Sarah E, Montgomery Grant W, Kandler Christian, McAdams Tom A, Eley Thalia C, Gregory Alice M, Saudino Kimberly J, Dubois Lise, Boivin Michel, Tarnoki Adam D, Tarnoki David L, Haworth Claire M A, Plomin Robert, Öncel Sevgi Y, Aliev Fazil, Stazi Maria A, Fagnani Corrado, D'Ippolito Cristina, Craig Jeffrey M, Saffery Richard, Siribaddana Sisira H, Hotopf Matthew, Sumathipala Athula, Rijsdijk Fruhling, Spector Timothy, Mangino Massimo, Lachance Genevieve, Gatz Margaret, Butler David A, Bayasgalan Gombojav, Narandalai Danshiitsoodol, Freitas Duarte L, Maia José Antonio, Harden K Paige, Tucker-Drob Elliot M, Kim Bia, Chong Youngsook, Hong Changhee, Shin Hyun Jung, Christensen Kaare, Skytthe Axel, Kyvik Kirsten O, Derom Catherine A, Vlietinck Robert F, Loos Ruth J F, Cozen Wendy, Hwang Amie E, Mack Thomas M, He Mingguang, Ding Xiaohu, Chang Billy, Silberg Judy L, Eaves Lindon J, Maes Hermine H, Cutler Tessa L, Hopper John L, Aujard Kelly, Magnusson Patrik K E, Pedersen Nancy L, Aslan Anna K Dahl, Song Yun-Mi, Yang Sarah, Lee Kayoung, Baker Laura A, Tuvblad Catherine, Bjerregaard-Andersen Morten, Beck-Nielsen Henning, Sodemann Morten, Heikkilä Kauko, Tan Qihua, Zhang Dongfeng, Swan Gary E, Krasnow Ruth, Jang Kerry L, Knafo-Noam Ariel, Mankuta David, Abramson Lior, Lichtenstein Paul, Krueger Robert F, McGue Matt, Pahlen Shandell, Tynelius Per, Duncan Glen E, Buchwald Dedra, Corley Robin P, Huibregtse Brooke M, Nelson Tracy L, Whitfield Keith E, Franz Carol E, Kremen William S, Lyons Michael J, Ooki Syuichi, Brandt Ingunn, Nilsen Thomas Sevenius, Inui Fujio, Watanabe Mikio, Bartels Meike, van Beijsterveldt Toos C E M, Wardle Jane, Llewellyn Clare H, Fisher Abigail, Rebato Esther, Martin Nicholas G, Iwatani Yoshinori, Hayakawa Kazuo, Sung Joohon, Harris Jennifer R, Willemsen Gonneke, Busjahn Andreas, Goldberg Jack H, Rasmussen Finn, Hur Yoon-Mi, Boomsma Dorret I, Sørensen Thorkild I A, Kaprio Jaakko, Silventoinen Karri

Zygosity Differences in Height and Body Mass Index of Twins From Infancy to Old Age: A Study of the CODATwins Project.

Twin research and human genetics : the official journal of the International Society for Twin Studies 2015; 18(5):557-70.

Kochunov P, Jahanshad N, Sprooten E, Nichols TE, Mandl RC, Almasy L, Booth T, Brouwer RM, Curran JE, de Zubicaray GI, Dimitrova R, Duggirala R, Fox PT, Hong LE, Landman BA, Lemaitre H, Lopez L, Martin NG, McMahon KL, Mitchell BD, Olvera RL, Peterson CP, Starr JM, Sussmann JE, Toga AW, Wardlaw JM, Wright MJ, Wright SN, Bastin ME, McIntosh AM, Boomsma DI, Kahn RS, den Braber A, de Geus EJ, Deary IJ, Hulshoff Pol HE, Williamson DE, Blangero J, van 't Ent D, Thompson PM, Glahn DC

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and mega analytical approaches for data pooling

NeuroImage 2014; 95:136-150.

Kochunov Peter, Jahanshad Neda, Sprooten Emma, Nichols Thomas E, Mandl René C, Almasy Laura, Booth Tom, Brouwer Rachel M, Curran Joanne E, de Zubicaray Greig I, Dimitrova Rali, Duggirala Ravi, Fox Peter T, Hong L Elliot, Landman Bennett A, Lemaitre Hervé, Lopez Lorna M, Martin Nicholas G, McMahon Katie L, Mitchell Braxton D, Olvera Rene L, Peterson Charles P, Starr John M, Sussmann Jessika E, Toga Arthur W, Wardlaw Joanna M, Wright Margaret J, Wright Susan N, Bastin Mark E, McIntosh Andrew M, Boomsma Dorret I, Kahn René S, den Braber Anouk, de Geus Eco J C, Deary Ian J, Hulshoff Pol Hilleke E, Williamson Douglas E, Blangero John, van 't Ent Dennis, Thompson Paul M, Glahn David C

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling.

NeuroImage 2014; 95:136-50.

Wright FA, Sullivan PF, Brooks AI, Zou F, Sun W, Xia K, Madar V, Jansen R, Chung W, Zhou YH

Heritability and genomics of gene expression in peripheral blood

Nature genetics 2014; 46(5):430-437.

Sullivan P F, de Geus E J C, Willemsen G, James M R, Smit J H, Zandbelt T, Arolt V, Baune B T, Blackwood D, Cichon S, Coventry W L, Domschke K, Farmer A, Fava M, Gordon S D, He Q, Heath A C, Heutink P, Holsboer F, Hoogendijk W J, Hottenga J J, Hu Y, Kohli M, Lin D, Lucae S, Macintyre D J, Maier W, McGhee K A, McGuffin P, Montgomery G W, Muir W J, Nolen W A, Nöthen M M, Perlis R H, Pirlo K, Posthuma D, Rietschel M, Rizzu P, Schosser A, Smit A B, Smoller J W, Tzeng J-Y, van Dyck R, Verhage M, Zitman F G, Martin N G, Wray N R, Boomsma D I, Penninx B W J H

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo.

Molecular psychiatry 2009; 14(4):359-75.

Trichotillomania / Compulsive Hoarding / Obsessive-Compulsive Disorder

Simpson HB, Foa EB, Wheaton MG, Gallagher T, Gershkovich M, Schmidt AB, Huppert JD, Campeas RB, Imms PA, Cahill S, DiChiara C, Tsao S, Puliafico A, Chazin D, Asnaani A, Moore K, Tyler J, Steinman SA, Sanchez-LaCay A, Capaldi S, Snorrason I, Turk-Karan E, Vermes D, Kalanthroff E, Pinto A, Hahn CG, Xu B, Van Meter P, Katechis M, Scodes J, Wang Y

Maximizing Remission from Cognitive-Behavioral Therapy in Medicated Adults with Obsessive-Compulsive Disorder

Behaviour research and therapy 2021; 143:103890.

McGuire Joseph F, Orr Scott P, Essoe Joey K-Y, McCracken James T, Storch Eric A, Piacentini John

Extinction learning in childhood anxiety disorders, obsessive compulsive disorder and posttraumatic stress disorder: implications for treatment

Expert review of neurotherapeutics 2016; 16(10):1155–1174.

McGuire Joseph F, Orr Scott P, Wu Monica S, Lewin Adam B, Small Brent J, Phares Vicky, Murphy Tanya K, Wilhelm Sabine, Pine Daniel S, Geller Daniel, Storch Eric A

Fear Conditioning and Extinction in Youth with Obsessive Compulsive Disorder

Depression and anxiety 2016; 33(3):229–237.

Storch Eric A., Wilhelm Sabine, Sprich Susan, Henin Aude, Micco Jamie, Small Brent J., McGuire Joseph, Mutch P. Jane, Lewin Adam B., Murphy Tanya K., Geller Daniel A.

Efficacy of Augmentation of Cognitive Behavior Therapy With Weight-Adjusted d-Cycloserine vs Placebo in Pediatric Obsessive-Compulsive Disorder: A Randomized Clinical Trial

JAMA Psychiatry 2016; 73(8):779-788.

De Nadai Alessandro, Nagpal Prianka S, Piacentini John, Peris Tara S, Geffken Gary R, Geller Daniel A, Murphy Tanya K, Storch Eric A, Lewin Adam B

Contemporary Models of Pediatric Obsessive Compulsive Disorder: An Evaluation with a Large Clinical Sample

Psychiatry research 2015; 229(1-2):620–622.

McGuire Joseph F, Piacentini John, Lewin Adam B, Brennan Erin A, Murphy Tanya K, Storch Eric A

A Meta-Analysis of Cognitive Behavior Therapy and Medication for Child Obsessive Compulsive Disorder: Moderators of Treatment Efficacy, Response, and Remission

Depression and anxiety 2015; 32(8):580–593.

McGuire Joseph F, Arnold Elysse, Park Jennifer M, Nadeau Joshua M, Lewin Adam B, Murphy Tanya K, Storch Eric A

Living with Tics: Reduced Impairment and Improved Quality of Life for Youth with Chronic Tic Disorders

Psychiatry research 2015; 225(3):571–579.

Fang A, Matheny NL, Wilhelm S

Body dysmorphic disorder

Psychiatric Clinics of North America 2014; 37(3):287-300.

Lewin AB, Wu MS, McGuire JF, Storch EA

Cognitive behavior therapy for obsessive-compulsive and related disorders

Psychiatric Clinics of North America 2014; 37(3):415-45.

McGuire Joseph F, Ung Danielle, Selles Robert R, Rahman Omar, Lewin Adam B, Murphy Tanya K, Storch Eric A

Treating Trichotillomania: A Meta-Analysis of Treatment Effects and Moderators for Behavior Therapy and Serotonin Reuptake Inhibitors

Journal of psychiatric research 2014; 58:76-83.

McGuire Joseph F, Lewin Adam B, Storch Eric A

Enhancing Exposure Therapy for Anxiety Disorders, Obsessive Compulsive Disorder, and Posttraumatic Stress Disorder

Expert review of neurotherapeutics 2014; 14(8):893–910.

Murphy TK, Gerardi DM, Leckman JF

Pediatric acute-onset neuropsychiatric syndrome

Psychiatric Clinics of North America 2014; 37(3):353-374.

Sulkowski Michael L, Geller Daniel A, Lewin Adam B, Murphy Tanya K, Mittelman Andrew, Brown Ashley, Storch Eric A

The Future of D-Cycloserine and Other Cognitive Modifiers in Obsessive-Compulsive and Related Disorders

Psychiatry research 2014; 10(4):317–324.

Goes FS, McCusker MG, Bienvenu OJ, MacKinnon DF, Mondimore FM, Schweizer B, DePaulo JR Jr, Potash JB

Co-morbid anxiety disorders in bipolar disorder and major depression : familial aggregation and clinical characteristics of co-morbid panic disorder, social phobia, specific phobia and obsessive-compulsive disorder

Psychological medicine 2012; 42(7):1449-1459.

McGuire Joseph F, Lewin Adam B, Geller Daniel A, Brown Ashley, Ramsey Kesley, Mutch Jane, Mittelman Andrew, Micco Jamie, Jordan Cary, Wilhelm Sabine, Murphy Tanya K, Small Brent J, Storch Eric A

Advances in the treatment of pediatric obsessive–compulsive d-cycloserine with exposure and response prevention

Neuropsychiatry (London) 2012; 2(4):.

Samuels JF, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Pinto A, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Bienvenu OJ 3rd, Rasmussen SA, Pauls DL, Willour VL, Shugart YY, Liang KY, Hoehn-Saric R, Nestadt G

The OCD Collaborative Genetics Study: Methods and Sample Description

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2006; 141B(3):201-207.

Krishnan KRR

Psychiatric and medical comorbidities of bipolar disorder

Psychosomatic medicine 2005; 67(1):1-8.

Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

Proceedings of the National Academy of Sciences of the United States of America 2005; 102(32):11545-11550.

Phelan-McDermid Syndrome

Otowa T, Hek K, Lee M, Byrne EM, Mirza SS, Nivard MG, Bigdeli T, Aggen SH, Adkins D, Wolen A, Fanous A, Keller MC, Castelao E, Kutalik Z, Van der Auwera S, Homuth G, Nauck M, Teumer A, Milaneschi Y, Hottenga JJ, Direk N, Hofman A, Uitterlinden A, Mulder CL, Henders AK, Medland SE, Gordon S, Heath AC, Madden PA, Pergadia M, van der Most PJ, Nolte IM, van Oort FV, Hartman CA, Oldehinkel AJ, Preisig M, Grabe HJ, Middeldorp CM, Penninx BW, Boomsma D, Martin NG, Montgomery G, Maher BS, van den Oord EJ, Wray NR, Tiemeier H, Hettema JM

Meta-analysis of genome-wide association studies of anxiety disorders

Molecular psychiatry 2016; 10.1038/mp.2015.197.

Research Domain Criteria

Hess JL, Nguyen NH, Suben J, Meath RM, Albert AB, Van Orman S, Anders KM, Forken PJ, Roe CA, Schulze TG, Faraone SV, Glatt SJ

Gene co-expression networks in peripheral blood capture dimensional measures of emotional and behavioral problems from the Child Behavior Checklist (CBCL)

Translational Psychiatry 2020; 10:328.

Sonabend W. A, Pellegrini AM, Chan S, Brown HE, Rosenquist JN, Vuijk PJ, Doyle AE, Perlis RH, Cai T

Integrating questionnaire measures for transdiagnostic psychiatric phenotyping using word2vec

PLoS ONE 2020; 15(4):e0230663.

McLean SA, Ressler K, Koenen KC, Neylan T, Germine L, Jovanovic T, Clifford GD, Zeng D, An X, Linnstaedt S, Beaudoin F, House S, Bollen KA, Musey P, Hendry P, Jones CW, Lewandowski C, Swor R, Datner E, Mohiuddin K, Stevens JS, Storrow A, Kurz MC, McGrath ME, Fermann GJ, Hudak LA, Gentile N, Chang AM, Peak DA, Pascual JL, Seamon MJ, Sergot P, Peacock WF, Diercks D, Sanchez LD, Rathlev N, Domeier R, Haran JP, Pearson C, Murty VP, Insel TR, Dagum P, Onnela JP, Bruce SE, Gaynes BN, Joormann J, Miller MW, Pietrzak RH, Buysse DJ, Pizzagalli DA, Rauch SL, Harte SE, Young LJ, Barch DM, Lebois LA, van Rooij SJ, Luna B, Smoller JW, Dougherty RF, Pace TW, Binder E, Sheridan JF, Elliott JM, Basu A, Fromer M, Parlikar T, Zaslavsky AM, Kessler R

The AURORA Study: A Longitudinal, Multimodal Library of Brain Biology and Function after Traumatic Stress Exposure

Molecular psychiatry 2019; 25(2):283-296.

Hinshaw SM, Makrantoni V, Kerr A, Marston AL, Harrison SC

Structural evidence for Scc4-dependent localization of cohesin loading

eLife 2015; 4:e06057.

Kukurba KR, Parsana P, Smith KS, Zappala Z, Knowles DA, Favé MJ, Li X, Zhu X, Potash JB, Weissman MM

Impact of the X chromosome and sex on regulatory variation

bioRxiv 2015; 024117.

Drago A, Giegling I, Schäfer M, Hartmann AM, Konte B, Friedl M, Serretti A, Rujescu D

Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment

Pharmacogenetics and genomics 2014; 24(6):314-319.

Hartz SM, Pato CN, Medeiros H, Cavazos-Rehg P, Sobell JL, Knowles JA, Bierut LJ, Pato MT

Comorbidity of severe psychotic disorders with measures of substance use

JAMA psychiatry 2014; 71(3):248-254.

Clarke TK, Bloch PJ, Ambrose-Lanci LM, Doyle GA, Ferraro TN, Berrettini WH, Kampman KM, Dackis CA, Pettinati HM, O'Brien CP

Further evidence for association between genetic variants in the cannabinoid receptor 1 (CNR1) gene and cocaine dependence: Confirmation in an independent sample and meta-analysis

Addiction biology 2013; 18(4):702-708.

Crist RC, Ambrose-Lanci LM, Zeng A, Yuan C, Kampman KM, Pettinati HM, Oslin DW, O'Brien CP, Ferraro TN, Doyle GA, Lohoff FW, Berrettini WH

Case-control association study of WLS variants in opioid and cocaine addicted populations

Psychiatry research 2013; 208(1):62-66.

Camera AA, Tomaselli V, Fleming J, Jabbar GA, Trachtenberg M, Galvez-Buccollini JA, Proal AC, Rosenthal RN, DeLisi LE

Correlates to the variable effects of cannabis in young adults: a preliminary study

Harm Reduction Journal 2012; 9:15.

Pirooznia M, Seifuddin F, Judy J, Mahon PB, Potash JB, Zandi PP

Data Mining Approaches for Genome-Wide Association of Mood Disorders

Psychiatric Genetics 2012; 22(2):55-61.

Saccone S, Chesler E, Haendel M

Applying in silico integrative genomics to genetic studies of human disease

Bioinformatics of Behavior: Part 2012; 1(103):133-156.

Xu H, Cheng C, Devidas M, Pei D, Fan Y, Yang W, Neale G, Scheet P, Burchard EG, Torgerson DG, Eng C, Dean M, Antillon F, Winick NJ, Martin PL, Willman CL, Camitta BM, Reaman GH, Carroll WL, Loh M, Evans WE, Pui CH, Hunger SP, Relling MV, Yang JJ

ARID5B Genetic Polymorphisms Contribute to Racial Disparities in the Incidence and Treatment Outcome of Childhood Acute Lymphoblastic Leukemia

Journal of Clinical Oncology 2012; 30(7):751-757.

Sarajärvi T, Tuusa JT, Haapasalo A, Lackman JJ, Sormunen R, Helisalmi S, Roehr JT, Parrado AR, Mäkinen P, Bertram L, Soininen H, Tanzi RE, Petäjä-Repo UE, Hiltunen M

Cysteine 27 Variant of the δ-Opioid Receptor Affects Amyloid Precursor Protein Processing through Altered Endocytic Trafficking

Molecular and Cellular Biology 2011; 31(11):2326-2340.

Mahon PB, Stütz AM, Seifuddin F, Huo Y, Goes FS, Jancic D, Judy JT, DePaulo JR Jr, Gershon ES, McMahon FJ, Zandi PP, Potash JB, Willour VL

Case-Control Association Study of TGOLN2 in Attempted Suicide

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 0(5):1016-1023.

Barrett JC, Clayton D, Concannon P, Akolkar B, Cooper JD, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Plagnol V, Pociot F, Schuilenburg H, Smyth DJ, Stevens H, Todd JA, Walker NM, Rich SS

Genome-wide association study and meta-analysis finds over 40 loci affect risk of type 1 diabetes

Nature genetics 2009; 41(6):703-707.

Mahon P, Payne J, MacKinnon D, Mondimore F, Goes F, Schweizer B, Jancic D, Coryell W, Holmans P, Shi J, Knowles J, Scheftner W, Weissman M, Levinson D, DePaulo J Jr, Zandi P, Potash J

Genome-wide linkage and follow-up association study of postpartum mood symptoms

The American journal of psychiatry 2009; 166(11):1229-1237.

Distel MA, Hottenga JJ, Trull TJ, Boomsma DI

Chromosome 9: linkage for borderline personality disorder features

Psychiatric Genetics 2008; 18(6):302-307.

Graham RR, Cotsapas C, Davies L, Hackett R, Lessard CJ, Leon JM, Burtt NP, Guiducci C, Parkin M, Gates C, Plenge RM, Behrens TW, Wither JE, Rioux JD, Fortin PR, Graham DC, Wong AK, Vyse TJ, Daly MJ, Altshuler D, Moser KL, Gaffney PM

Genetic Variants Near TNFAIP3 on 6q23 are Associated with Systemic Lupus Erythematosus (SLE)

Nature genetics 2008; 40(9):1059-1061.

van den Oord EJCG, Kuo PH, Hartmann AM, Webb BT, Möller HJ, Hettema JM, Giegling I, Bukszár J, Rujescu D

Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism

Archives of general psychiatry 2008; 65(9):1062-1071.

Eaton WW, Hall ALF, Macdonald R, Mckibben J

Case identification in psychiatric epidemiology: a review

International Review of Psychiatry 2007; 19(5):497-507.

Sanders AR, Duan J, Gejman PV

Complexities in psychiatric genetics

International Review of Psychiatry 2004; 16(4):284-293.

Badenhop RF, Moses MJ, Scimone A, Adams LJ, Kwok JBJ, Jones AM, Davison G, Evans MR, Kirkby KC, Hewitt JE

Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 117(1):23-32.

Duan J, Sanders AR, Vander Molen JE, Martinolich L, Mowry BJ, Levinson DF, Crowe RR, Silverman JM, Gejman PV

Polymorphisms in the 5′-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression

Molecular psychiatry 2003; 8(11):901-910.

Haukim N, Bidwell JL, Smith AJ, Keen LJ, Gallagher G, Kimberly R, Huizinga T, McDermott MF, Oksenberg J, McNicholl J

Cytokine gene polymorphism in human disease: on-line databases, supplement 2

Genes and immunity 2002; 3(6):313-330.

Merikangas KR, Chakravarti A, Moldin SO, Araj H, Blangero J, Burmeister M, Crabbe JC, Depaulo JR, Foulks E, Freimer NB

Future of genetics of mood disorders research

Biological psychiatry 2002; 52(6):457-477.

Nurnberger Jr JI

Park City, Utah Molecular Psychiatry Meeting, February 2001

Psychiatric genetics 2001; 11(1):1-4.

Buxbaum JD, Lilliehook C, Chan JY, Go RCP, Bassett SS, Tanzi RE, Wasco W, Blacker D

Genomic structure, expression pattern, and chromosomal localization of the human calsenilin gene: no association between an exonic polymorphism and Alzheimer's disease

Neuroscience letters 2000; 294(3):135-138.

Yoshikawa T, Padigaru M, Karkera JD, Sharma M, Berrettini WH, Esterling LE, Detera-Wadleigh SD

Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)

Molecular psychiatry 2000; 5(2):165-171.

Armstrong C

Chromosome workshop: chromosomes 11, 14, and 15

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1999; 88:244-254.

Detera-Wadleigh SD, Barden N, Craddock N, Ewald H, Foroud T, Kelsoe J, McQuillin A

Chromosomes 12 and 16 workshop

American journal of medical genetics 1999; 88(3):255-259.

Nurnberger J

Park City, Utah Molecular Psychiatry Meeting, February 1998.

Psychiatric genetics 1999; 9(2):59-62.

Nurnberger JI, Blehar MC, Kaufmann CA, York-Cooler C, Simpson SG, Harkavy-Friedman J, Severe JB, Malaspina D, Reich T

Diagnostic interview for genetic studies: rationale, unique features, and training

Archives of general psychiatry 1994; 51(11):849-859.

Schizophrenia

Fabbri C, Leggio GM, Drago F, Serretti A

Imputed expression of schizophrenia-associated genes and cognitive measures in patients with schizophrenia

Molecular Genetics & Genomic Medicine 2022; 10(6):e1942.

Gregory MD, Eisenberg DP, Hamborg M, Kippenhan JS, Kohn P, Kolachana B, Dickinson D, Berman KF

Neanderthal-Derived Genetic Variation in Living Humans Relates to Schizophrenia Diagnosis, to Psychotic Symptom Severity, and to Dopamine Synthesis

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2021; 186(5):329-338.

Hindley G, Bahrami S, Steen NE, O'Connell KS, Frei O, Shadrin A, Bettella F, Rødevand L, Fan CC, Dale AM, Djurovic S, Smeland OB, Andreassen OA

Characterising the shared genetic determinants of bipolar disorder, schizophrenia and risk-taking

Translational Psychiatry 2021; 11:466.

Hu B, Won H, Mah W, Park RB, Kassim B, Spiess K, Kozlenkov A, Crowley CA, Pochareddy S, Li Y, Dracheva S, Sestan N, Akbarian S, Geschwind DH

Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

Nature Communications 2021; 12:3968.

Pak C, Danko T, Mirabella VR, Wang J, Liu Y, Vangipuram M, Grieder S, Zhang X, Ward T, Huang YW, Jin K, Dexheimer P, Bardes E, Mitelpunkt A, Ma J, McLachlan M, Moore JC, Qu P, Purmann C, Dage JL, Swanson BJ, Urban AE, Aronow BJ, Pang ZP, Levinson DF, Wernig M, Südhof TC

Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons

Proceedings of the National Academy of Sciences of the United States of America 2021; 118(22):e2025598118.

Huang G, Osorio D, Guan J, Ji G, Cai JJ

Overdispersed gene expression in schizophrenia

NPJ Schizophrenia 2020; 6:9.

Lee KY, Leung KS, Ma SL, So HC, Huang D, Tang NL, Wong MH

Genome-Wide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets

Frontiers in Genetics 2020; 11:1003.

McClain L, Mansour H, Klei L, Fathi W, Wood J, Kodavali C, Maysterchuk A, Wood S, Ibrahim I, Ibrahim N, Eissa A, El-Bahaei W, El Sayed H, Yassein A, Tobar S, El-Boraie H, Elsheshtawy E, Salah H, Ali A, Erdin S, Devlin B, Talkowski M, Nimgaonkar V

Age Dependent Association of Inbreeding with Risk for Schizophrenia in Egypt

Schizophrenia research 2020; 216:450-459.

Chen J, Wu JS, Mize T, Moreno M, Hamid M, Servin F, Bashy B, Zhao Z, Jia P, Tsuang MT, Kendler KS, Xiong M, Chen X

A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population

Scientific Reports 2019; 9:12717.

de Vrij Femke M, Bouwkamp Christian G, Gunhanlar Nilhan, Shpak Guy, Lendemeijer Bas, Baghdadi Maarouf, Gopalakrishna Shreekara, Ghazvini Mehrnaz, Li Tracy M, Quadri Marialuisa, Olgiati Simone, Breedveld Guido J, Coesmans Michiel, Mientjes Edwin, de Wit Ton, Verheijen Frans W, Beverloo H Berna, Cohen Dan, Kok Rob M, Bakker P Roberto, Nijburg Aviva, Spijker Annet T, Haffmans P M Judith, Hoencamp Erik, Bergink Veerle, Vorstman Jacob A, Wu Timothy, Olde Loohuis Loes M, Amin Najaf, Langen Carolyn D, Hofman Albert, Hoogendijk Witte J, van Duijn Cornelia M, Ikram M Arfan, Vernooij Meike W, Tiemeier Henning, Uitterlinden André G, Elgersma Ype, Distel Ben, Gribnau Joost, White Tonya, Bonifati Vincenzo, Kushner Steven A

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.

Molecular psychiatry 2019; 24(5):757-771.

Doostparast Torshizi A, Armoskus C, Zhang H, Forrest MP, Zhang S, Souaiaia T, Evgrafov OV, Knowles JA, Duan J, Wang K

Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia

Science Advances 2019; 5(9):eaau4139.

Fang G, Wang W, Paunic V, Heydari H, Costanzo M, Liu X, Liu X, VanderSluis B, Oately B, Steinbach M, Van Ness B, Schadt EE, Pankratz ND, Boone C, Kumar V, Myers CL

Discovering genetic interactions bridging pathways in genome-wide association studies

Nature Communications 2019; 10:4274.

Jonas Katherine, Clouston Sean, Li Kaiqiao, Fochtmann Laura J, Lencz Todd, Malhotra Anil K, Cicero David, Perlman Greg, Bromet Evelyn J, Kotov Roman

Apolipoprotein E-ε4 allele predicts escalation of psychotic symptoms in late adulthood.

Schizophrenia research 2019; 206:82-88.

Mullins N, Bigdeli TB, Børglum AD, Coleman JR, Demontis D, Fanous AH, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A, Corvin A, Sanders AR, Forstner AJ, Reif A, Koller AC, Świątkowska B, Baune BT, Müller-Myhsok B, Konte B, Penninx BW, Pato C, Zai C, Rujescu D, Hougaard DM, Quested D, Levinson DF, Binder EB, Byrne EM, Agerbo E, Streit F, Mayoral F, Bellivier F, Degenhardt F, Breen G, Morken G, Turecki G, Rouleau GA, Grabe HJ, Völzke H, Jones I, Giegling I, Agartz I, Melle I, Lawrence J, Potash JB, Walters JT, Strohmaier J, Shi J, Hauser J, Biernacka JM, Vincent JB, Kelsoe J, Strauss JS, Lissowska J, Pimm J, Smoller JW, Guzman Parra J, Berger K, Scott LJ, Jones LA, Azevedo MH, Trzaskowski M, Kogevinas M, Rietschel M, Boks M, Ising M, Grigoroiu-Serbanescu M, Hamshere ML, Leboyer M, Frye M, Nöthen MM, Alda M, Preisig M, Nordentoft M, Boehnke M, O'Donovan MC, Owen MJ, Pato MT, Renteria M, Budde M, Weissman MM, Wray NR, Bass N, Craddock N, Smeland OB, Andreassen OA, Mors O, Gejman PV, Sklar P, McGrath P, Hoffmann P, McGuffin P, Lee PH, Mortensen PB, Kahn RS, Ophoff RA, Adolfsson R, Van der Auwera S, Djurovic S, Shyn SI, Kloiber S, Heilmann-Heimbach S, Jamain S, Hamilton SP, McElroy SL, Lucae S, Cichon S, Schulze TG, Hansen T, Werge T, Air TM, Nimgaonkar V, Appadurai V, Cahn W, Milaneschi Y, Kendler KS, McQuillin A, Lewis CM

Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

The American journal of psychiatry 2019; 176(8):651-660.

Ramos EM, Dokuru DR, Van Berlo V, Wojta K, Wang Q, Huang AY, Miller ZA, Karydas AM, Bigio EH, Rogalski E, Weintraub S, Rader B, Miller BL, Gorno-Tempini ML, Mesulam MM, Coppola G

Genetic screen in a large series of patients with primary progressive aphasia

Alzheimer's & dementia : the journal of the Alzheimer's Association 2019; 15(4):553-560.

Schrode N, Ho SM, Yamamuro K, Dobbyn A, Huckins L, Matos MR, Cheng E, Deans PJ, Flaherty E, Barretto N, Topol A, Alganem K, Abadali S, Gregory J, Hoelzli E, Phatnani H, Singh V, Girish D, Aronow B, Mccullumsmith R, Hoffman GE, Stahl EA, Morishita H, Sklar P, Brennand KJ

Synergistic effects of common schizophrenia risk variants

Nature genetics 2019; 51(10):1475-1485.

Spertus J, Horvitz-Lennon M, Normand SL

Bayesian Meta-Analysis of Multiple Continuous Treatments with Individual Participant-Level Data: An Application to Antipsychotic Drugs

Medical decision making : an international journal of the Society for Medical Decision Making 2019; 39(5):583-592.

Duan J, Göring HH, Sanders AR, Moy W, Freda J, Drigalenko EI, Kos M, He D, Gejman PV

Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model

Translational Psychiatry 2018; 8:158.

Liu Y, Chang X, Hahn CG, Gur RE, Sleiman PA, Hakonarson H

Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease

Translational Psychiatry 2018; 8:44.

Maier RM, Zhu Z, Lee SH, Trzaskowski M, Ruderfer DM, Stahl EA, Ripke S, Wray NR, Yang J, Visscher PM, Robinson MR

Improving genetic prediction by leveraging genetic correlations among human diseases and traits

Nature Communications 2018; 9:989.

Readhead Benjamin, Hartley Brigham J, Eastwood Brian J, Collier David A, Evans David, Farias Richard, He Ching, Hoffman Gabriel, Sklar Pamela, Dudley Joel T, Schadt Eric E, Savić Radoslav, Brennand Kristen J

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia.

Nature communications 2018; 9(1):4412.

Xavier RM, Dungan JR, Keefe RS, Vorderstrasse A

Polygenic signal for symptom dimensions and cognitive performance in patients with chronic schizophrenia

Schizophrenia Research: Cognition 2018; 12:11-19.

Xu J, Hartley B J, Kurup P, Phillips A, Topol A, Xu M, Ononenyi C, Foscue E, Ho S-M, Baguley T D, Carty N, Barros C S, Müller U, Gupta S, Gochman P, Rapoport J, Ellman J A, Pittenger C, Aronow B, Nairn A C, Nestor M W, Lombroso P J, Brennand K J

null

Molecular psychiatry 2018; 23(2):271-281.

DeMichele-Sweet MA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, Lopez OL, Sibille EL, Kamboh MI, Devlin B, Sweet RA

Genetic Risk for Schizophrenia and Psychosis in Alzheimer Disease

Molecular psychiatry 2017; 10.1038/mp.2017.81.

Doyle GA, Crist RC, Karatas ET, Hammond MJ, Ewing AD, Ferraro TN, Hahn CG, Berrettini WH

Analysis of LINE-1 Elements in DNA from Postmortem Brains of Individuals with Schizophrenia

Neuropsychopharmacology 2017; 42(13):2602-2611.

Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PM, Li Q, Hakonarson H

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genome Medicine 2017; 9:106.

He P, Lei X, Yuan D, Zhu Z, Huang S

Accumulation of minor alleles and risk prediction in schizophrenia

Scientific Reports 2017; 7:11661.

Liu C, Bousman CA, Pantelis C, Skafidas E, Zhang D, Yue W, Everall IP

Pathway-wide association study identifies five shared pathways associated with schizophrenia in three ancestral distinct populations

Translational Psychiatry 2017; 7(2):e1037-.

McLaughlin RL, Schijven D, van Rheenen W, van Eijk KR, O'Brien M, Kahn RS, Ophoff RA, Goris A, Bradley DG, Al-Chalabi A, van den Berg LH, Luykx JJ, Hardiman O, Veldink JH

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

Nature Communications 2017; 8:14774.

Pinsonneault JK, Frater JT, Kompa B, Mascarenhas R, Wang D, Sadee W

Intronic SNP in ESR1 encoding human estrogen receptor alpha is associated with brain ESR1 mRNA isoform expression and behavioral traits

PLoS ONE 2017; 12(6):e0179020.

Sanders AR, Drigalenko EI, Duan J, Moy W, Freda J, Göring HH, Gejman PV

Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis

Translational Psychiatry 2017; 7(4):e1093-.

Woolston AL, Hsiao PC, Kuo PH, Wang SH, Lien YJ, Liu CM, Hwu HG, Lu TP, Chuang EY, Chang LC, Chen CH, Wu JY, Tsuang MT, Chen WJ

Genetic loci associated with an earlier age at onset in multiplex schizophrenia

Scientific Reports 2017; 7:6486.

Zhu L, Lei J, Devlin B, Roeder K

TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES

The annals of applied statistics 2017; 11(3):1810-1831.

Chen TH, Sun W, Fine JP

Designing penalty functions in high dimensional problems: The role of tuning parameters

Electronic journal of statistics 2016; 10(2):2312-2328.

Chen J, Bacanu SA, Yu H, Zhao Z, Jia P, Kendler KS, Kranzler HR, Gelernter J, Farrer L, Minica C

Genetic Relationship between Schizophrenia and Nicotine Dependence

Scientific reports 2016; 6:.

Clifton NE, Pocklington AJ, Scholz B, Rees E, Walters JT, Kirov G, O'Donovan MC, Owen MJ, Wilkinson LS, Thomas KL, Hall J

Schizophrenia copy number variants and associative learning

Molecular Psychiatry 2016; 22(2):178-182.

Cocchi E, Drago A, Serretti A

Hippocampal Pruning as a New Theory of Schizophrenia Etiopathogenesis

Mol Neurobiol 2016

Greenwood TA, Light GA, Swerdlow NR, Calkins ME, Green MF, Gur RE, Gur RC, Lazzeroni LC, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Freedman R, Braff DL

Gating Deficit Heritability and Correlation with Increased Clinical Severity in Schizophrenia Patients with Positive Family History

Am J Psychiatry 2016

Han J, Walters JT, Kirov G, Pocklington A, Escott-Price V, Owen MJ, Holmans P, O'Donovan MC, Rees E

Gender differences in CNV burden do not confound schizophrenia CNV associations

Scientific Reports 2016; 6:25986.

Lee M, Aggen SH, Otowa T, Castelao E, Preisig M, Grabe HJ, Hartman CA, Oldehinkel AJ, Middeldorp CM, Tiemeier H, Hettema JM

Assessment and Characterization of Phenotypic Heterogeneity of Anxiety Disorders across Five Large Cohorts

International journal of methods in psychiatric research 2016; 25(4):255-266.

Martin PM, Stanley RE, Ross AP, Freitas AE, Moyer CE, Brumback AC, Iafrati J, Stapornwongkul KS, Dominguez S, Kivimäe S, Mulligan KA, Pirooznia M, McCombie WR, Potash JB, Zandi PP, Purcell SM, Sanders SJ, Zuo Y, Sohal VS, Cheyette BN

DIXDC1 contributes to psychiatric susceptibility by regulating dendritic spine and glutamatergic synapse density via GSK3 and Wnt/β-catenin signaling

Molecular psychiatry 2016; 10.1038/mp.2016.184.

Millard SP, Shofer J, Braff D, Calkins M, Cadenhead K, Freedman R, Green MF, Greenwood TA, Gur R, Gur R, Lazzeroni LC, Light GA, Olincy A, Nuechterlein K, Seidman L, Siever L, Silverman J, Stone W, Sprock J, Sugar CA, Swerdlow NR, Tsuang M, Turetsky B, Radant A, Tsuang DW

Prioritizing Schizophrenia Endophenotypes for Future Genetic Studies: An Example Using Data from the COGS-1 Family Study

Schizophrenia research 2016; 174(1-3):1-9.

Rees E, Kendall K, Pardiñas AF, Legge SE, Pocklington A, Escott-Price V, MacCabe JH, Collier DA, Holmans P, O'Donovan MC, Owen MJ, Walters JT, Kirov G

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

JAMA psychiatry 2016; 73(9):963-969.

Topol Aaron, Zhu Shijia, Hartley Brigham J, English Jane, Hauberg Mads E, Tran Ngoc, Rittenhouse Chelsea Ann, Simone Anthony, Ruderfer Douglas M, Johnson Jessica, Readhead Ben, Hadas Yoav, Gochman Peter A, Wang Ying-Chih, Shah Hardik, Cagney Gerard, Rapoport Judith, Gage Fred H, Dudley Joel T, Sklar Pamela, Mattheisen Manuel, Cotter David, Fang Gang, Brennand Kristen J

Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells.

Cell reports 2016; 15(5):1024-1036.

Zuo L, Tan Y, Li CS, Wang Z, Wang K, Zhang X, Lin X, Chen X, Zhong C, Wang X, Guo X, Wang J, Lu L, Luo X

Associations of rare nicotinic cholinergic receptor gene variants to nicotine and alcohol dependence

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016; 171(8):1057-1071.

Buckley PF, Schooler NR, Goff DC, Hsiao J, Kopelowicz A, Lauriello J, Manschreck T, Mendelowitz AJ, Miller del D, Severe JB, Wilson DR, Ames D, Bustillo J, Mintz J, Kane JR, PROACTIVE Study

Comparison of SGA oral medications and a long-acting injectable SGA: the PROACTIVE study

Schizophr Bull 2015; 41(2):449-459.

Cocchi E, Drago A, Serretti A

Hippocampal Pruning as a New Theory of Schizophrenia Etiopathogenesis

Molecular neurobiology 2015; 1-17.

Crisafulli C, Drago A, Calabrò M, Spina E, Serretti A

A molecular pathway analysis informs the genetic background at risk for schizophrenia

Prog Neuropsychopharmacol 2015; 59:21-30.

Gur RC, Braff DL, Calkins ME, Dobie DJ, Freedman R, Green MF, Greenwood TA, Lazzeroni LC, Light GA, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Sprock J, Stone WS, Sugar CA, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Gur RE

Neurocognitive performance in family-based and case-control studies of schizophrenia

Schizophr Res 2015; 163(1-3):17-23.

Hartley B J, Tran N, Ladran I, Reggio K, Brennand K J

Dopaminergic differentiation of schizophrenia hiPSCs.

Molecular psychiatry 2015; 20(5):549-50.

Huentelman MJ, Muppana L, Corneveaux JJ, Dinu V, Pruzin JJ, Reiman R, Borish CN, De Both M, Ahmed A, Todorov A, Cloninger CR, Zhang R, Ma J, Gallitano AL

Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk

PLoS ONE 2015; 10(10):e0135076.

Johnson EO, Hancock DB, Levy JL, Gaddis NC, Page GP, Glasheen C, Saccone NL, Bierut LJ, Kral AH

KAT2B Polymorphism Identified for Drug Abuse in African Americans with Regulatory Links to Drug Abuse Pathways in Human Prefrontal Cortex

Addiction biology 2015; 21(6):1217-1232.

Kennedy JL, Xiong N, Yu J, Zai CC, Pouget JG, Li J, Liu K, Qing H, Wang T, Martin E, Levy DL, Lin Z

Increased Nigral SLC6A3 Activity in Schizophrenia Patients: Findings From the Toronto-McLean Cohorts

Schizophrenia Bulletin 2015; 42(3):772-781.

Kerner B

Comorbid substance use disorders in schizophrenia: A latent class approach

Psychiatry research 2015; 225(3):395-401.

Lee IS, Carvalho CM, Douvaras P, Ho SM, Hartley BJ, Zuccherato LW, Ladran IG, Siegel AJ, McCarthy S, Malhotra D, Sebat J, Rapoport J, Fossati V, Lupski JR, Levy DL, Brennand KJ

Characterization of molecular and cellular phenotypes associated with a heterozygous CNTNAP2 deletion using patient-derived hiPSC neural cells

NPJ Schizophrenia 2015; 1:15019-.

Lee Inkyu S, Carvalho Claudia M B, Douvaras Panagiotis, Ho Seok-Man, Hartley Brigham J, Zuccherato Luciana W, Ladran Ian G, Siegel Arthur J, McCarthy Shane, Malhotra Dheeraj, Sebat Jonathan, Rapoport Judith, Fossati Valentina, Lupski James R, Levy Deborah L, Brennand Kristen J

null

NPJ schizophrenia 2015; 1:.

Perez-Andreu V, Roberts KG, Xu H, Smith C, Zhang H, Yang W, Harvey RC, Payne-Turner D, Devidas M, Cheng IM, Carroll WL, Heerema NA, Carroll AJ, Raetz EA, Gastier-Foster JM, Marcucci G, Bloomfield CD, Mrózek K, Kohlschmidt J, Stock W, Kornblau SM, Konopleva M, Paietta E, Rowe JM, Luger SM, Tallman MS, Dean M, Burchard EG, Torgerson DG, Yue F, Wang Y, Pui CH, Jeha S, Relling MV, Evans WE, Gerhard DS, Loh ML, Willman CL, Hunger SP, Mullighan CG, Yang JJ

A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults

Blood 2015; 125(4):680-686.

Radant AD, Millard SP, Braff DL, Calkins ME, Dobie DJ, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Lazzeroni LC, Light GA, Meichle SP, Nuechterlein KH, Olincy A, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Sugar CA, Tsuang MT, Turetsky BI, Tsuang DW

Robust differences in antisaccade performance exist between COGS schizophrenia cases and controls regardless of recruitment strategies

Schizophr Res 2015; 163(1-3):47-52.

Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanaugh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Tsuang MT, Glatt SJ, Chen WJ, Hwu HG; Taiwanese Trios Exome Sequencing Consortium, Neale BM, Palotie A, Sklar P, Purcell SM, McCarroll SA, Holmans P, Owen MJ, O'Donovan MC

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

Transl Psychiatry 2015; 5:e607.

Seidman LJ, Hellemann G, Nuechterlein KH, Greenwood TA, Braff DL, Cadenhead KS, Calkins ME, Freedman R, Gur RE, Gur RC

Factor structure and heritability of endophenotypes in schizophrenia: Findings from the Consortium on the Genetics of Schizophrenia (COGS-1)

Schizophrenia research 2015; 163(1):73-79.

Zhao Z, Xu J, Chen J, Kim S, Reimers M, Bacanu SA, Yu H, Liu C, Sun J, Wang Q

Transcriptome sequencing and genome-wide association analyses reveal lysosomal function and actin cytoskeleton remodeling in schizophrenia and bipolar disorder

Molecular psychiatry 2015; 20(5):563-572.

Dickinson D, Straub RE, Trampush JW, Gao Y, Feng N, Xie B, Shin JH, Lim HK, Ursini G, Bigos KL, Kolachana B, Hashimoto R, Takeda M, Baum GL, Rujescu D, Callicott JH, Hyde TM, Berman KF, Kleinman JE, Weinberger DR

Differential effects of common variants in SCN2A on general cognitive ability, brain physiology, and messenger RNA expression in schizophrenia cases and control individuals.

JAMA Psychiatry 2014; 71(6):647-656.

Duan Jubao, Shi Jianxin, Fiorentino Alessia, Leites Catherine, Chen Xiangning, Moy Winton, Chen Jingchun, Alexandrov Boian S, Usheva Anny, He Deli, Freda Jessica, O'Brien Niamh L, McQuillin Andrew, Sanders Alan R, Gershon Elliot S, DeLisi Lynn E, Bishop Alan R, Gurling Hugh M D, Pato Michele T, Levinson Douglas F, Kendler Kenneth S, Pato Carlos N, Gejman Pablo V

A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder.

American journal of human genetics 2014; 95(6):744-53.

Duan J, Shi J, Fiorentino A, Leites C, Chen X, Moy W, Chen J, Alexandrov BS, Usheva A, He D, Freda J, O'Brien NL, McQuillin A, Sanders AR, Gershon ES, DeLisi LE, Bishop AR, Gurling HM, Pato MT, Levinson DF, Kendler KS, Pato CN, Gejman PV

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

American Journal of Human Genetics 2014; 95(6):744-753.

Juraeva D, Haenisch B, Zapatka M, Frank J, Witt SH, Mühleisen TW, Treutlein J, Strohmaier J, Meier S, Degenhardt F, Giegling I, Ripke S, Leber M, Lange C, Schulze TG, Mössner R, Nenadic I, Sauer H, Rujescu D, Maier W, Børglum A, Ophoff R, Cichon S, Nöthen MM, Rietschel M, Mattheisen M, Brors B

Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

PLoS Genetics 2014; 10(6):e1004345.

Liang SG, Greenwood TA

The Impact of Clinical Heterogeneity in Schizophrenia on Genomic Analyses

Schizophrenia research 2014; 161(0):490-495.

McEvoy JP, Byerly M, Hamer RM, Dominik R, Swartz MS, Rosenheck RA, Ray N, Lamberti JS, Buckley PF, Wilkins TM, Stroup TS

Effectiveness of paliperidone palmitate vs haloperidol decanoate for maintenance treatment of schizophrenia: a randomized clinical trial

JAMA 2014; 312(14):1473.

Mulle JG, Pulver AE, McGrath JM, Wolyniec P, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, Gejman PV, Sanders AR, Duan J, Mitchell AA, Peter I, Sklar P, O'Dushlaine CT, Grozeva D, O'Donovan MC, Owen MJ, Hultman CM, Kähler AK, Sullivan PF, Kirov G, Warren ST

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

Biological psychiatry 2014; 75(5):371-377.

Nurnberger JI Jr, Koller DL, Jung J, Edenberg HJ, Foroud T, Guella I, Vawter MP, Kelsoe JR

Identification of Pathways for Bipolar Disorder A Meta-analysis

JAMA psychiatry 2014; 71(6):657-664.

Ripke S, Neale BM, Corvin A, Walters JTR, Farh KH, Holmans PA, Lee P, Bulik-Sullivan B, Collier DA, Huang H

Biological insights from 108 schizophrenia-associated genetic loci

Nature 2014; 511(7510):421-427.

Rodriguez-Murillo L, Xu B, Roos JL, Abecasis GR, Gogos JA, Karayiorgou M

Fine Mapping on Chromosome 13q32-34 and Brain Expression Analysis Implicates MYO16 in Schizophrenia

Neuropsychopharmacology 2014; 39(4):934-943.

Schmeidler J, Lazzeroni LC, Swerdlow NR, Ferreira RP, Braff DL, Calkins ME, Cadenhead KS, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Olincy A, Nuechterlein KH, Radant AD, Seidman LJ, Siever LJ, Stone WS, Sprock J, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Silverman JM

Paternal age of schizophrenia probands and endophenotypic differences from unaffected siblings

Psychiatry Res 2014; 219(1):67-71.

Swerdlow NR, Light GA, Sprock J, Calkins ME, Green MF, Greenwood TA, Gur RE, Gur RC, Lazzeroni LC, Nuechterlein KH, Radant AD, Ray A, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL

Deficient prepulse inhibition in schizophrenia detected by the multi-site COGS

Schizophr Res 2014; 152(2-3):503-512.

Vieland VJ, Walters KA, Lehner T, Azaro M, Tobin K, Huang Y, Brzustowicz LM

Revisiting Schizophrenia Linkage Data in the NIMH Repository: Reanalysis of Regularized Data Across Multiple Studies

The American journal of psychiatry 2014; 171(3):350-359.

Vieland VJ, Walters KA, Azaro M, Brzustowicz LM, Lehner T

The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels

Hum Hered 2014; 78(1):9-16.

Vieland VJ, Walters KA, Azaro M, Brzustowicz LM, Lehner T

The value of regenotyping older linkage data sets with denser marker panels

Human heredity 2014; 78(1):9-16.

Walters KA, Huang Y, Azaro M, Tobin K, Lehner T, Brzustowicz LM, Vieland VJ

Meta-Analysis of Repository Data: Impact of Data Regularization on NIMH Schizophrenia Linkage Results

PLoS ONE 2014; 9(1):e84696.

Wang KS, Zuo L, Owusu D, Pan Y, Luo X

Prostate Cancer Related JAZF1 Gene is Associated with Schizophrenia

Journal of schizophrenia research 2014; 1(1):6.

Agim ZS, Esendal M, Briollais L, Uyan O, Meschian M, Martinez LA, Ding Y, Basak AN, Ozcelik H

Discovery, Validation and Characterization of Erbb4 and Nrg1 Haplotypes Using Data from Three Genome-Wide Association Studies of Schizophrenia

PLoS ONE 2013; 8(1):e53042.

Balan S, Yamada K, Hattori E, Iwayama Y, Toyota T, Ohnishi T, Maekawa M, Toyoshima M, Iwata Y, Suzuki K, Kikuchi M, Yoshikawa T

Population-Specific Haplotype Association of the Postsynaptic Density Gene DLG4 with Schizophrenia, in Family-Based Association Studies

PLoS ONE 2013; 8(7):e70302.

Calkins ME, Ray A, Gur RC, Freedman R, Green MF, Greenwood TA, Light GA, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar C, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL, Lazzeroni LC, Gur RE

Sex differences in familiality effects on neurocognitive performance in schizophrenia

Biol Psychiatry 2013; 73(10):976-984.

Chang SH, Gao L, Li Z, Zhang WN, Du Y, Wang J

BDgene: a genetic database for bipolar disorder and its overlap with schizophrenia and major depressive disorder

Biological psychiatry 2013; 74(10):727-733.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ, Hewitt JK, Goddard ME, O'Donovan MC, Purcell SM, Posthuma D, Visscher PM, Wray NR, Keller MC

Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

American Journal of Human Genetics 2013; 93(3):463-470.

Giegling I, Balzarro B, Porcelli S, Schäfer M, Hartmann AM, Friedl M, Konte B, Krämer P, Möller HJ, De Ronchi D

Influence of ANKK1 and DRD2 polymorphisms in response to haloperidol

European archives of psychiatry and clinical neuroscience 2013; 263(1):65-74.

Goudriaan A, de Leeuw C, Ripke S, Hultman CM, Sklar P, Sullivan PF, Smit AB, Posthuma D, Verheijen MH

Specific Glial Functions Contribute to Schizophrenia Susceptibility

Schizophrenia Bulletin 2013; 40(4):925-935.

Gulsuner S, Walsh T, Watts AC, Lee MK, Thornton AM, Casadei S, Rippey C, Shahin H, Nimgaonkar VL, Go RCP

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

Cell 2013; 154(3):518-529.

Huey ED, Nagy PL, Rodriguez-Murillo L, Manochehri M, Goldman J, Lieberman J, Karayiorgou M, Mayeux R

C9ORF72 repeat expansions not detected in a group of patients with schizophrenia

Neurobiology of aging 2013; 34(4):1309.e9-1309.10.

Jackson KJ, Fanous AH, Chen J, Kendler KS, Chen X

Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder

Psychiatric genetics 2013; 23(1):20-28.

Kirov G, Rees E, Walters JT, Escott-Price V, Georgieva L, Richards AL, Chambert KD, Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ

The penetrance of copy number variations for schizophrenia and developmental delay

Biological psychiatry 2013; 75(5):378-385.

Lencz T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L, Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nöthen MM, Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisanté A, Gregersen PK, Pe'er I, Malhotra AK, Goldman D, Darvasi A

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

Nature Communications 2013; 4:2739.

Lencz T, Knowles E, Davies G, Guha S, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, Lundervold A, Steen VM, John M, Espeseth T, Räikkönen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Ikeda M, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Horan M, Donohoe G, Morris D, Corvin A, Gill M, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Hellard SL, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK

Molecular Genetic Evidence for Genetic Overlap between General Cognitive Ability and Risk for Schizophrenia: A Report from the Cognitive Genomics Consortium (COGENT)

Molecular psychiatry 2013; 19(2):168-174.

Lien YJ, Huang SS, Liu CM, Hwu HG, Faraone SV, Tsuang MT, Chen WJ

A Genome-wide Quantitative Linkage Scan of Niacin Skin Flush Response in Families With Schizophrenia

Schizophrenia Bulletin 2013; 39(1):68-76.

Pato MT, Sobell JL, Medeiros H, Abbott C, Skar B, Buckley PF, Bromet EJ, Escamilla MA, Fanous AH, Lehrer DS, Macciardi F, Malaspina D, McCarroll SA, Marder SR, Moran J, Morley CP, Nicolini H, Perkins DO, Purcell SM, Rapaport MH, Sklar P, Smoller JW, Knowles JA, Pato CN

The Genomic Psychiatry Cohort: Partners in Discovery

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 0(4):306-312.

Perez-Andreu V, Roberts KG, Harvey RC, Yang W, Cheng C, Pei D, Xu H, Gastier-Foster J, Shuyu E, Yew-Suang Lim J, Chen IM, Fan Y, Devidsa M, Borowitz MJ, Smith C, Neale G, Burchard EG, Torgerson DG, Klussmann FA, Villagran CR, Winick NJ, Camitta BM, Raetz E, Wood B, Yue F, Carroll WL, Larsen E, Bowman WP, Loh ML, Dean M, Bhojwani D, Pui CH, Evans WE, Relling MV, Hunger SP, Willman CL, Mullighan CG, Yang JJ

Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse

Nature genetics 2013; 45(12):1494-1498.

Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Human Molecular Genetics 2013; 23(6):1669-1676.

Rippey C, Walsh T, Gulsuner S, Brodsky M, Nord AS, Gasperini M, Pierce S, Spurrell C, Coe BP, Krumm N

Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia

The American Journal of Human Genetics 2013; 93(4):697-710.

Sanders AR, Göring HH, Duan J, Drigalenko EI, Moy W, Freda J, He D, Shi J, Gejman PV

Transcriptome study of differential expression in schizophrenia

Human Molecular Genetics 2013; 22(24):5001-5014.

Sanders AR, Göring HHH, Duan J, Drigalenko EI, Moy W, Freda J, He D, Shi J, Gejman PV

Transcriptome study of differential expression in schizophrenia

Human molecular genetics 2013; ddt350.

Shcheglovitov A, Shcheglovitova O, Yazawa M, Portmann T, Shu R, Sebastiano V, Krawisz A, Froehlich W, Bernstein JA, Hallmayer JF, Dolmetsch RE

SHANK3 and IGF1 restore synaptic deficits in neurons from 11q13 deletion syndrome patients

Nature 2013; 503(7475):267-271.

Sleiman P, Wang D, Glessner J, Hadley D, Gur RE, Cohen N, Li Q, Hakonarson H, Janssen-CHOP Neuropsychiatric Genomics Working Group

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia/Bipolar susceptibility locus

Scientific reports 2013; 3:.

Takahashi S

Heterogeneity of schizophrenia: Genetic and symptomatic factors

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2013; 162(7):648-652.

Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T

A population-specific uncommon variant in GRIN3A associated with schizophrenia

Biological psychiatry 2013; 73(6):532-539.

Timms AE, Dorschner MO, Wechsler J, Choi KY, Kirkwood R, Girirajan S, Baker C, Eichler EE, Korvatska O, Roche KW

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families

JAMA psychiatry 2013; 70(6):582-590.

Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Larach-Walters V, Insel PA, Karayiorgou M, DeLisi LE, Sebat J

Compositions And Methods For The Diagnosis of Schizophrenia

Xu C, Aragam N, Li X, Villla EC, Wang L, Briones D, Petty L, Posada Y, Arana TB, Cruz G, Mao C, Camarillo C, Su BB, Escamilla MA, Wang K

BCL9 and C9orf5 Are Associated with Negative Symptoms in Schizophrenia: Meta-Analysis of Two Genome-Wide Association Studies

PLoS ONE 2013; 8(1):e51674.

Zhao Z, Webb BT, Jia P, Bigdeli TB, Maher BS, van den Oord E, Bergen SE, Amdur RL, O'Neill FA, Walsh D, Thiselton DL, Chen X, Pato CN, Riley BP, Kendler KS, Fanous AH

Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis

PLoS ONE 2013; 8(7):e67776.

Åberg K, Khachane AN, Rudolf G, Nerella S, Fugman DA, Tischfield JA, van den Oord EJ

Methylome-wide comparison of human genomic DNA extracted from whole blood and from EBV-transformed lymphocyte cell lines

European Journal of Human Genetics 2012; 20(9):953-955.

Ambrose-Lanci LM, Vaswani M, Clarke TK, Zeng A, Lohoff FW, Ferraro TN, Berrettini WH

Association study of the β-arrestin 2 gene (ARRB2) with opioid and cocaine dependence in a European American population

Psychiatric genetics 2012; 22(3):141-145.

Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, Salomon D, Schork NJ, Fanous AH, O'Donovan MC, Niculescu AB

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction

Molecular Psychiatry 2012; 17(9):887-905.

Bae JS, Pasaje CFA, Park BL, Cheong HS, Kim JH, Kim JY, Shin JG, Park CS, Kim BJ, Lee CS

Genetic association analysis of ERBB4 polymorphisms with the risk of schizophrenia and SPEM abnormality in a Korean population

Brain research 2012; 1466:146-151.

Chen J, Brunzell DH, Jackson K, van der Vaart A, Ma JZ, Payne TJ, Sherva R, Farrer LA, Gejman P, Levinson DF, Holmans P, Aggen SH, Damaj I, Kuo PH, Webb BT, Anton R, Kranzler HR, Gelernter J, Li MD, Kendler KS, Chen X

Correction: ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure

PLoS ONE 2012; 7(8):10.1371/annotation/071abcbd-6f0c-4c4b-9507-dae42450457e.

Chen C, Cheng L, Grennan K, Pibiri F, Zhang C, Badner JA, Gershon ES, Liu C

Two Gene Co-expression Modules Differentiate Psychotics and Controls

Molecular psychiatry 2012; 18(12):1308-1314.

Coppola G, Chinnathambi S, Lee JJ, Dombroski BA, Baker MC, Soto-Ortolaza AI, Lee SE, Klein E, Huang AY, Sears R, Lane JR, Karydas AM, Kenet RO, Biernat J, Wang LS, Cotman CW, DeCarli CS, Levey AI, Ringman JM, Mendez MF, Chui HC, Le Ber I, Brice A, Lupton MK, Preza E, Lovestone S, Powell J, Graff-Radford N, Petersen RC, Boeve BF, Lippa CF, Bigio EH, Mackenzie I, Finger E, Kertesz A, Caselli RJ, Gearing M, Juncos JL, Ghetti B, Spina S, Bordelon YM, Tourtellotte WW, Frosch MP, Vonsattel JP, Zarow C, Beach TG, Albin RL, Lieberman AP, Lee VM, Trojanowski JQ, Van Deerlin VM, Bird TD, Galasko DR, Masliah E, White CL, Troncoso JC, Hannequin D, Boxer AL, Geschwind MD, Kumar S, Mandelkow EM, Wszolek ZK, Uitti RJ, Dickson DW, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Ross OA, Rademakers R, Schellenberg GD, Miller BL, Mandelkow E, Geschwind DH

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

Human Molecular Genetics 2012; 21(15):3500-3512.

Debono R, Topless R, Markie D, Black MA, Merriman TR

Analysis of the DISC1 translocation partner (11q14.3) in genetic risk of schizophrenia

Genes, brain, and behavior 2012; 11(7):859-863.

Drago A, Giegling I, Schäfer M, Hartmann AM, Möller HJ, De Ronchi D, Stassen HH, Serretti A, Rujescu D

No Association of a Set of Candidate Genes on Haloperidol Side Effects

PLoS ONE 2012; 7(10):e44853.

Epstein MP, Duncan R, Broadaway KA, He M, Allen AS, Satten GA

Stratification Score Matching Improves Correction for Confounding by Population Stratification in Case-Control Association Studies

Genetic epidemiology 2012; 36(3):195-205.

Ferguson JP, Cho JH, Yang C, Zhao H

Empirical Bayes Correction for the Winner's Curse in Genetic Association Studies

Genetic epidemiology 2012; 37(1):60-68.

Gladwin TE, Derks EM, Rietschel M, Mattheisen M, Breuer R, Schulze TG, Nöthen MM, Levinson D, Shi J, Gejman PV, Cichon S, Ophoff RA

Segment-Wise Genome-Wide Association Analysis Identifies a Candidate Region Associated with Schizophrenia in Three Independent Samples

PLoS ONE 2012; 7(6):e38828.

Heinzen EL, Depondt C, Cavalleri GL, Ruzzo EK, Walley NM, Need AC, Ge D, He M, Cirulli ET, Zhao Q, Cronin KD, Gumbs CE, Campbell CR, Hong LK, Maia JM, Shianna KV, McCormick M, Radtke RA, O'Conner GD, Mikati MA, Gallentine WB, Husain AM, Sinha SR, Chinthapalli K, Puranam RS, McNamara JO, Ottman R, Sisodiya SM, Delanty N, Goldstein DB

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

Am J Hum Genet 2012; 91(2):293-302.

Jia P, Wang L, Fanous AH, Pato CN, Edwards TL, Zhao Z

Network-Assisted Investigation of Combined Causal Signals from Genome-Wide Association Studies in Schizophrenia

PLoS Computational Biology 2012; 8(7):e1002587.

Kim S, Millard SP, Yu CE, Leong L, Radant A, Dobie D, Tsuang DW, Wijsman EM

Inheritance Model Introduces Differential Bias in CNV Calls between Parents and Offspring

Genetic epidemiology 2012; 36(5):488-498.

Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S, Dudbridge F, Holmans PA

Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees

The American journal of psychiatry 2012; 169(9):963-973.

Liu Q, Jamba M, Patrick C III, Padmanabhan S, Brennan MD

Targeted pharmacogenetic analysis of antipsychotic response in the CATIE study

Pharmacogenomics 2012; 13(11):1227-1237.

Liu Q, Ramsey TL, Meltzer HY, Massey BW, Padmanabhan S, Brennan MD

Sulfotransferase 4A1 haplotype 1 (SULT4A1-1) is associated with decreased hospitalization events in antipsychotic-treated patients with schizophrenia

The primary care companion to CNS disorders 2012; 14(3):.

McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, Donald JA, Weickert CS, Mitchell PB, Schofield PR, Fullerton JM

Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26

PLoS ONE 2012; 7(5):e38172.

Need AC, McEvoy JP, Gennarelli M, Heinzen EL, Ge D, Maia JM, Shianna KV, He M, Cirulli ET, Gumbs CE, Zhao Q, Campbell CR, Hong L, Rosenquist P, Putkonen A, Hallikainen T, Repo-Tiihonen E, Tiihonen J, Levy DL, Meltzer HY, Goldstein DB

Exome sequencing followed by large-scale genotyping suggests a limited role for moderate rare risk factors of strong effect in schizophrenia

Am J Hum Genet 2012; 91(2):303-312.

Sequeira A, Martin MV, Rollins B, Moon EA, Bunney WE, Macciardi F, Lupoli S, Smith EN, Kelsoe J, Magnan CN, van Oven M, Baldi P, Wallace DC, Vawter MP

Mitochondrial Mutations and Polymorphisms in Psychiatric Disorders

Frontiers in Genetics 2012; 3:103.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E, Hougaard DM, Ørntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Milovancevic MP, Tosevski DL, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K

Common Variant at 16p11.2 Conferring Risk of Psychosis

Molecular psychiatry 2012; 19(1):10.1038/mp.2012.157.

Stephens SH, Franks A, Berger R, Palionyte M, Fingerlin TE, Wagner B, Logel J, Olincy A, Ross RG, Freedman R, Leonard S

Multiple genes in the 15q13-q14 chromosomal region are associated with schizophrenia

Psychiatric genetics 2012; 22(1):10.1097/YPG.0b013e32834c0c33.

Van Dorn RA, Desmarais SL, Young MS, Sellers BG, Swartz MS

Assessing illicit drug use among adults with schizophrenia

Psychiatry research 2012; 200(2-3):228-236.

Wang C, Krishnakumar S, Wilhelmy J, Babrzadeh F, Stepanyan L, Su LF, Levinson D, Fernandez-Viña MA, Davis RW, Davis MM

High-throughput, high-fidelity HLA genotyping with deep sequencing

Proceedings of the National Academy of Sciences 2012; 109(22):8676-8681.

Yamada K, Iwayama Y, Toyota T, Ohnishi T, Ohba H, Maekawa M, Yoshikawa T

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population

Human Genetics 2012; 131(3):443-451.

Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

BMC Pregnancy and Childbirth 2012; 12:61.

Buckley PF, Pillai A, Schooler NR, Miller DD, Goff D, Kopelowicz A, Lauriello J, Manschreck T, Mendelowitz A, Wilson D, Kane JM

Brain Derived Neurotrophic Factor as a Potential Biomarker for Relapse in Schizophrenia: Initial Observations from the PROACTIVE (Preventing Relapse in Schizophrenia: Oral Antipsychotics Compared to Injectables: Evaluating Efficacy) Study

Schizophr Bull 2011; 37:83-83.

Chen X, Lee G, Maher B S, Fanous A H, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan P F, Shi J, Levinson D F, Gejman P V, Sanders A, Duan J, Owen M J, Craddock N J, O'Donovan M C, Blackman J, Lewis D, Kirov G K, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub R E, Weinberger D R, O'Neill F A, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra A K, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen M M, Rietschel M, Cichon S, Djurovic S, Andreassen O A, Cantor R M, Ophoff R, Corvin A, Morris D W, Gill M, Pato C N, Pato M T, Macedo A, Gurling H M D, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell S M, Scolnick E, St Clair D, Blackwood D H R, Kendler K S

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.

Molecular psychiatry 2011; 16(11):1117-29.

Chen J, Lee G, Fanous AH, Zhao Z, Jia P, O'Neill A, Walsh D, Kendler KS, Chen X, International Schizophrenia Consortium

Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia

Schizophrenia research 2011; 131(1):43-51.

Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

Molecular psychiatry 2011; 16(11):1117-1129.

Hermes E, Nasrallah H, Davis V, Meyer J, McEvoy J, Goff D, Davis S, Stroup S, Swartz M, Lieberman J, Rosenheck R

The Association Between Weight Change And Symptom Reduction in the CATIE Schizophrenia Trial

Schizophrenia research 2011; 128(0):166-170.

Jia P, Zhao Z

Network-assisted Causal Gene Detection in Genome-wide Association Studies: An Improved Module Search Algorithm

IEEE International Workshop on Genomic Signal Processing and Statistics : [proceedings]. IEEE International Workshop on Genomic Signal Processing and Statistics 2011; 131-134.

Kendler KS, Kalsi G, Holmans PA, Sanders AR, Aggen SH, Dick DM, Aliev F, Shi J, Levinson DF, Gejman PV

Association Analysis of Symptoms of Alcohol Dependence in the Molecular Genetics of Schizophrenia (MGS2) Control Sample

Alcoholism, clinical and experimental research 2011; 35(5):963-975.

Lee S, Wright FA, Zou AF

Control of population stratification by correlation-selected principal components

Biometrics 2011; 67(3):967-974.

Levinson Douglas F, Duan Jubao, Oh Sang, Wang Kai, Sanders Alan R, Shi Jianxin, Zhang Nancy, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Kendler Kenneth S, Freedman Robert, Dudbridge Frank, Pe'er Itsik, Hakonarson Hakon, Bergen Sarah E, Fanous Ayman H, Holmans Peter A, Gejman Pablo V

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.

The American journal of psychiatry 2011; 168(3):302-16.

Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Kendler KS, Freedman R, Dudbridge F, Pe'er I, Hakonarson H, Bergen SE, Fanous AH, Holmans PA, Gejman PV

Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications

The American journal of psychiatry 2011; 168(3):302-316.

Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

American Journal of Psychiatry 2011

Lien YJ, Hsiao PC, Liu CM, Faraone SV, Tsuang MT, Hwu HG, Chen WJ

A Genome-Wide Linkage Scan for Distinct Subsets of Schizophrenia Characterized by Age at Onset and Neurocognitive Deficits

PLoS ONE 2011; 6(8):e24103.

Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman CM, Holmans PA, O'Donovan MC, Purcell SM, Smit AB, Verhage M, Sullivan PF, Visscher PM, Posthuma D

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

Molecular Psychiatry 2011; 17(10):996-1006.

Liu Y, Gibson J, Wheeler J, Kwee LC, Santiago-Turla CM, Akafo SK, Lichter PR, Gaasterland DE, Moroi SE, Challa P, Herndon LW, Girkin CA, Budenz DL, Richards JE, Allingham RR, Hauser MA

GALC Deletions Increase the Risk of Primary Open-Angle Glaucoma: The Role of Mendelian Variants in Complex Disease

PLoS ONE 2011; 6(11):e27134.

Ramsey Timothy L, Meltzer Herbert Y, Brock Guy N, Mehrotra Bharat, Jayathilake Karu, Bobo William V, Brennan Mark D

Evidence for a SULT4A1 haplotype correlating with baseline psychopathology and atypical antipsychotic response.

Pharmacogenomics 2011; 12(4):471-80.

Salvi E, Orro A, Guffanti G, Lupoli S, Torri F, Barlassina C, Potkin S, Cusi D, Macciardi F, Milanesi L

Population Stratification Analysis in Genome-Wide Association Studies

Steinberg S, de Jong S; Irish Schizophrenia Genomics Consortium, Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, Breuer R, Vassos E, Giegling I, Fraser G, Walker N, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Agartz I, Melle I, Djurovic S, Strengman E; GROUP, Jürgens G, Glenthøj B, Terenius L, Hougaard DM, Ørntoft T, Wiuf C, Didriksen M, Hollegaard MV, Nordentoft M, van Winkel R, Kenis G, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Sperling S, Rossner M, Ribolsi M, Magni V, Siracusano A, Christiansen C, Kiemeney LA, Veldink J, van den Berg L, Ingason A, Muglia P, Murray R, Nöthen MM, Sigurdsson E, Petursson H, Thorsteinsdottir U, Kong A, Rubino IA, De Hert M, Réthelyi JM, Bitter I, Jönsson EG, Golimbet V, Carracedo A, Ehrenreich H, Craddock N, Owen MJ, O'Donovan MC; Wellcome Trust Case Control Consortium 2, Ruggeri M, Tosato S, Peltonen L, Ophoff RA, Collier DA, St Clair D, Rietschel M, Cichon S, Stefansson H, Rujescu D, Stefansson K

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

Hum Mol Genet 2011; 20(20):4076-4081.

Stewart LR, Hall AL, Kang SHL, Shaw CA, Beaudet AL

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

BMC medical genetics 2011; 12(1):154.

Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, Craig D, Kelsoe JR, Gershon ES, Leal SM, Dell Aquila M, Morris DW, Gill M, Corvin A, Insel PA, McClellan J, King MC, Karayiorgou M, Levy DL, DeLisi LE, Sebat J

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.

Nature 2011; 471(7339):499-503.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X

SNP-based pathway enrichment analysis for genome-wide association studies

BMC Bioinformatics 2011; 12:99.

Yamada K, Iwayama Y, Hattori E, Iwamoto K, Toyota T, Ohnishi T, Ohba H, Maekawa M, Kato T, Yoshikawa T

Genome-Wide Association Study of Schizophrenia in Japanese Population

PLoS ONE 2011; 6(6):e20468.

Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, Levy DL, Ballif BC, Platky K, Farber DM, Gowans GC, Wetherbee JJ, Asamoah A, Weaver DD, Mark PR, Dickerson J, Garg BP, Ellingwood SA, Smith R, Banks VC, Smith W, McDonald MT, Hoo JJ, French BN, Hudson C, Johnson JP, Ozmore JR, Moeschler JB, Surti U, Escobar LF, El-Kechen D, Gorski JL, Kussman J, Salbert B, Lacassie Y, Biser A, McDonald-McGinn DM, Zackai EH, Deardorff MA, Shaikh TH, Haan E, Friend KL, Fichera M, Romano C, Gécz J, deLisi LE, Sebat J, King MC, Shaffer LG, Eichler EE

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Nature genetics 2010; 42(3):203-209.

Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PM, Flory JH, Imielinski M, Frackelton EC, Chiavacci R, Thomas KA, Garris M, Otieno FG, Davidson M, Weiser M, Reichenberg A, Davis KL, Friedman JI, Cappola TP, Margulies KB, Rader DJ, Grant SF, Buxbaum JD, Gur RE, Hakonarson H

Strong synaptic transmission impact by copy number variations in schizophrenia

Proceedings of the National Academy of Sciences of the United States of America 2010; 107(23):10584-10589.

Harris M, Gladman B, Hennessy N, Lloyd C, Mowry B, Waghorn G

Reliability of a scale of work-related self-efficacy for people with psychiatric disabilities

International Journal of Rehabilitation Research 2010; 33(2):183-186.

Huang J, Perlis RH, Lee PH, Rush AJ, Fava M, Sachs GS, Lieberman J, Hamilton SP, Sullivan P, Sklar P, Purcell S, Smoller JW

Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression

The American journal of psychiatry 2010; 167(10):10.1176/appi.ajp.2010.09091335.

Jackson K, Chen Q, Chen J, Aggen S, Kendler K, Chen X

Association of the histidine-triad nucleotide-binding protein-1 (HINT1) gene variants with nicotine dependence

The pharmacogenomics journal 2010; 11(4):251-257.

Jiménez-Castro L, Hare E, Medina R, Raventos H, Nicolini H, Mendoza R, Ontiveros A, Jerez A, Muñoz R, Dassori A, Escamilla M

Substance use disorder comorbidity with schizophrenia in families of Mexican and Central American Ancestry

Schizophrenia research 2010; 120(1-3):87-94.

Lien YJ, Liu CM, Faraone SV, Tsuang MT, Hwu HG, Hsiao PC, Chen WJ

A genome-wide quantitative trait loci scan of neurocognitive performances in families with schizophrenia

Genes, Brain and Behavior 2010; 9(7):695-702.

Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST

Microdeletions of 3q29 Confer High Risk for Schizophrenia

American Journal of Human Genetics 2010; 87(2):229-236.

Nicodemus KK, Law AJ, Radulescu E, Luna A, Kolachana B, Vakkalanka R, Rujescu D, Giegling I, Straub RE, McGee K, Gold B, Dean M, Muglia P, Callicott JH, Tan HY, Weinberger DR

NRG1, ERBB4 and AKT1 Epistasis Increases Schizophrenia Risk and is Biologically Validated via Functional Neuroimaging in Healthy Controls

Archives of general psychiatry 2010; 67(10):991-1001.

Olincy A, Braff DL, Adler LE, Cadenhead KS, Calkins ME, Dobie DJ, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Radant AD, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Wagner BD, Freedman R

Inhibition of the P50 cerebral evoked response to repeated auditory stimuli: results from the Consortium on Genetics of Schizophrenia

Schizophr Res 2010; 119(1-3):175-182.

Radant AD, Dobie DJ, Calkins ME, Olincy A, Braff DL, Cadenhead KS, Freedman R, Green MF, Greenwood TA, Gur RE, Gur RC, Light GA, Meichle SP, Millard SP, Mintz J, Nuechterlein KH, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang MT, Turetsky BI, Tsuang DW

Antisaccade performance in schizophrenia patients, their first-degree biological relatives, and community comparison subjects: Data from the COGS study

Psychophysiology 2010; 47(5):846-856.

Sanders AR, Levinson DF, Duan J, Dennis JM, Li R, Kendler KS, Rice JP, Shi J, Mowry BJ, Amin F, Silverman JM, Buccola NG, Byerley WF, Black DW, Freedman R, Cloninger CR, Gejman PV

The internet-based MGS2 control sample: Self report of mental illness

The American journal of psychiatry 2010; 167(7):854-865.

Sanders AR, Levinson DF, Duan J, Dennis JM, Li R, Kendler KS, Rice JP, Shi J, Mowry BJ, Amin F

The Internet-based MGS2 control sample: self report of mental illness

The American journal of psychiatry 2010

Sun J, Jia P, Fanous AH, van den Oord E, Chen X, Riley BP, Amdur RL, Kendler KS, Zhao Z

Schizophrenia Gene Networks and Pathways and Their Applications for Novel Candidate Gene Selection

PLoS ONE 2010; 5(6):e11351.

Talkowski ME, McCann KL, Chen M, McClain L, Bamne M, Wood J, Chowdari KV, Watson A, Prasad KM, Kirov G, Georgieva L, Toncheva D, Mansour H, Lewis DA, Owen M, O'Donovan M, Papasaikas P, Sullivan P, Ruderfer D, Yao JK, Leonard S, Thomas P, Miyajima F, Quinn J, Lopez AJ, Nimgaonkar VL

Fine-mapping reveals novel alternative splicing of the dopamine transporter

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010; 0(8):1434-1447.

Tsai Huei-Ting, Caroff Stanley N, Miller Del D, McEvoy Joseph, Lieberman Jeffrey A, North Kari E, Stroup T Scott, Sullivan Patrick F

A candidate gene study of Tardive dyskinesia in the CATIE schizophrenia trial.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010; 153B(1):336-40.

Tsuang DW, Millard SP, Ely B, Chi P, Wang K, Raskind WH, Kim S, Brkanac Z, Yu CE

The Effect of Algorithms on Copy Number Variant Detection

PLoS ONE 2010; 5(12):e14456.

Wallace C, Smyth DJ, Maisuria-Armer M, Walker NM, Todd JA, Clayton DG

The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes

Nature genetics 2010; 42(1):68-71.

Zou F, Lee S, Knowles MR, Wright FA

Quantification of Population Structure Using Correlated SNPs by Shrinkage Principal Components

Human Heredity 2010; 70(1):9-22.

Alkelai A, Greenbaum L, Rigbi A, Kanyas K, Lerer B

Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients

Psychopharmacology 2009; 206(3):491-499.

Escamilla M, Hare E, Dassori AM, Peralta JM, Ontiveros A, Nicolini H, Raventós H, Medina R, Mendoza R, Jerez A

A schizophrenia gene locus on chromosome 17q21 in a new set of families of Mexican and central american ancestry: evidence from the NIMH Genetics of schizophrenia in latino populations study

American Journal of Psychiatry 2009; 166(4):442-449.

Goes FS, Willour VL, Zandi PP, Belmonte PL, MacKinnon DF, Mondimore FM, Schweizer B, Gershon ES, McMahon FJ, Potash JB

Family-Based Association Study of Neuregulin 1 With Psychotic Bipolar Disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 0(5):693-702.

Holmans P, Riley B, Pulver A, Owen M, Wildenauer D, Gejman P, Mowry B, Laurent C, Kendler K, Nestadt G, Williams N, Schwab S, Sanders A, Nertney D, Mallet J, Wormley B, Lasseter V, O'Donovan M, Duan J, Albus M, Alexander M, Godard S, Ribble R, Liang K, Norton N, Maier W, Papadimitriou G, Walsh D, Jay M, O'Neill A, Lerer F, Dikeos D, Crowe R, Silverman J, Levinson D

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms

Molecular psychiatry 2009; 14(8):786-795.

Huffaker SJ, Chen J, Nicodemus KK, Sambataro F, Yang F, Mattay V, Lipska BK, Hyde TM, Song J, Rujescu D, Giegling I, Mayilyan K, Proust MJ, Soghoyan A, Caforio G, Callicott JH, Bertolino A, Meyer-Lindenberg A, Chang J, Ji Y, Egan MF, Goldberg TE, Kleinman JE, Lu B, Weinberger DR

A novel, primate-specific, brain isoform of KCNH2 impacts cortical physiology, cognition, neuronal repolarization and risk for schizophrenia

Nature medicine 2009; 15(5):509-518.

Mansour HA, Talkowski ME, Wood J, Chowdari KV, McClain L, Prasad K, Montrose D, Fagiolini A, Friedman ES, Allen MH, Bowden CL, Calabrese J, El-Mallakh RS, Escamilla M, Faraone SV, Fossey MD, Gyulai L, Loftis JM, Hauser P, Ketter TA, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel J, Sachs GS, Sklar P, Smoller JW, Laird N, Keshavan M, Thase ME, Axelson D, Birmaher B, Lewis D, Monk T, Frank E, Kupfer DJ, Devlin B, Nimgaonkar VL

Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia

Bipolar Disorders 2009; 11(7):701-710.

Sinkus ML, Lee MJ, Gault J, Logel J, Short M, Freedman R, Christian SL, Lyon J, Leonard S

A 2-Base Pair Deletion Polymorphism in the Partial Duplication of the α7 Nicotinic Acetylcholine Gene (CHRFAM7A) on Chromosome 15q14 is Associated with Schizophrenia

Brain research 2009; 1291:1-11.

Stephens SH, Logel J, Barton A, Franks A, Schultz J, Short M, Dickenson J, James B, Fingerlin TE, Wagner B, Hodgkinson C, Graw S, Ross RG, Freedman R, Leonard S

Association of the 5′-upstream regulatory region of the α7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophrenia

Schizophrenia research 2009; 109(1-3):102-112.

Sun J, Jia P, Fanous AH, Webb BT, van den Oord EJ, Chen X, Bukszar J, Kendler KS, Zhao Z

A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

Bioinformatics 2009; 25(19):2595-6602.

Talkowski ME, McClain L, Allen T, Bradford LD, Calkins M, Edwards N, Georgieva L, Go R, Gur R, Gur R, Kirov G, Chowdari K, Kwentus J, Lyons P, Mansour H, McEvoy J, O' Donovan MC, O'Jile J, Owen MJ, Santos A, Savage R, Toncheva D, Vockley G, Wood J, Devlin B, Nimgaonkar VL

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150B(4):560-569.

van den Oord EJCG, Adkins DE, McClay J, Lieberman J, Sullivan PF

A systematic method for estimating individual responses to treatment with antipsychotics in CATIE

Schizophrenia research 2009; 107(1):13-21.

Washizuka S, Iwamoto K, Kakiuchi C, Bundo M, Kato T

Expression of mitochondrial complex I subunit gene NDUFV2 in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia

Neuroscience research 2009; 63(3):199-204.

Wiener H, Klei L, Dickson M, Perry R, Aliyu M, Allen T, Bradford L, Calkins M, Devlin B, Edwards N, Gur R, Gur R, Kwentus J, Lyons P, McEvoy J, Nasrallah H, Nimgaonkar V, O'Jile J, Santos A, Savage R, Go R

Linkage analysis of schizophrenia in African-American families

Schizophrenia research 2009; 109(1-3):70-79.

Yamada K, Hattori E, Iwayama Y, Toyota T, Ohnishi T, Iwata Y, Tsuchiya KJ, Sugihara G, Kikuchi M, Okazaki Y

Failure to confirm genetic association of the CHI3L1 gene with schizophrenia in Japanese and Chinese populations

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150(4):508-514.

Almasy Laura, Gur Ruben C, Haack Karin, Cole Shelley A, Calkins Monica E, Peralta Juan Manuel, Hare Elizabeth, Prasad Konsale, Pogue-Geile Michael F, Nimgaonkar Vishwajit, Gur Raquel E

A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes.

The American journal of psychiatry 2008; 165(9):1185-92.

Budel S, Shim SO, Feng Z, Zhao H, Hisama F, Strittmatter SM

No association between schizophrenia and polymorphisms of the PlexinA2 gene in Chinese Han Trios

Schizophrenia research 2008; 99(1-3):365-366.

Budel S, Padukkavidana T, Liu BP, Feng Z, Hu F, Johnson S, Lauren J, Park JH, McGee AW, Liao J, Stillman A, Kim JE, Yang BZ, Sodi S, Gelernter J, Zhao H, Hisama F, Arnsten AF, Strittmatter SM

Genetic variants of Nogo-66 Receptor with possible association to schizophrenia block myelin inhibition of axon growth

The Journal of neuroscience : the official journal of the Society for Neuroscience 2008; 28(49):13161-13172.

Campbell Daniel B, Lange Leslie A, Skelly Tara, Lieberman Jeffrey, Levitt Pat, Sullivan Patrick F

Association of RGS2 and RGS5 variants with schizophrenia symptom severity.

Schizophrenia research 2008; 101(1-3):67-75.

Campbell Daniel B, Ebert Philip J, Skelly Tara, Stroup T Scott, Lieberman Jeffrey, Levitt Pat, Sullivan Patrick F

Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia.

Biological psychiatry 2008; 63(1):32-41.

Chao HM, Kao HT, Porton B

BDNF Val66Met variant and age of onset in schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(4):505-506.

Chowdari Kodavali V, Bamne Mikhil, Wood Joel, Talkowski Michael E, Mirnics Karoly, Levitt Pat, Lewis David A, Nimgaonkar Vishwajit L

Linkage disequilibrium patterns and functional analysis of RGS4 polymorphisms in relation to schizophrenia.

Schizophrenia bulletin 2008; 34(1):118-26.

Escamilla M, Lee BD, Ontiveros A, Raventos H, Nicolini H, Mendoza R, Jerez A, Munoz R, Medina R, Figueroa A

The epsin 4 gene is associated with psychotic disorders in families of Latin American origin

Schizophrenia research 2008; 106(2):253-257.

Grossman I, Sullivan PF, Walley N, Liu Y, Dawson JR, Gumbs C, Gaedigk A, Leeder JS, McEvoy JP, Weale ME, Goldstein DB

Genetic Determinants of Variable Metabolism Have Little Impact on the Clinical Use of Leading Antipsychotics in the CATIE study

Genetics in medicine : official journal of the American College of Medical Genetics 2008; 10(10):720-729.

Holliday E, Mowry B, Nyholt D

A reanalysis of 409 European-ancestry and African American families with schizophrenia reveals significant linkage to 8p23.3 with evidence of locus heterogeneity

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147B(7):1080-1088.

Kakiuchi C, Ishiwata M, Nanko S, Ozaki N, Iwata N, Umekage T, Tochigi M, Kohda K, Sasaki T, Imamura A

Up-regulation of ADM and SEPX1 in the lymphoblastoid cells of patients in monozygotic twins discordant for schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2008; 147(5):557-564.

Lohoff FW, Weller AE, Bloch PJ, Buono RJ, Doyle GA, Ferraro TN, Berrettini WH

Association between polymorphisms in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) on chromosome 8p and schizophrenia

Neuropsychobiology 2008; 57(1-2):55-60.

Sanders AR, Duan J, Levinson DF, Shi J, He D, Hou C, Burrell GJ, Rice JP, Nertney DA, Olincy A

No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics

The American journal of psychiatry 2008; 165(4):497-506.

Shi J, Gershon ES, Liu C

Genetic associations with schizophrenia: meta-analyses of 12 "top" genes

Schizophr Res 2008; 104(1-3):96-107.

Sullivan PF, Lin D, Tzeng JY, van den Oord E, Perkins D, Stroup TS, Wagner M, Lee S, Wright FA, Zou F, Liu W, Downing AM, Lieberman J, Close SL

Genomewide Association for Schizophrenia in the CATIE Study: Results of Stage 1

Molecular psychiatry 2008; 13(6):570-584.

Takahashi S, Cui YH, Han YH, Fagerness JA, Galloway B, Shen YC, Kojima T, Uchiyama M, Faraone SV, Tsuang MT

Association of SNPs and Haplotypes in APOL1, 2 and 4 with schizophrenia

Schizophrenia research 2008; 104(0):153-164.

Turetsky BI, Greenwood TA, Olincy A, Radant AD, Braff DL, Cadenhead KS, Dobie DJ, Freedman R, Green MF, Gur RE, Gur RC, Light GA, Mintz J, Nuechterlein KH, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Swerdlow NR, Tsuang DW, Tsuang MT, Calkins ME

Abnormal Auditory N100 Amplitude: A Heritable Endophenotype in First-Degree Relatives of Schizophrenia Probands

Biological psychiatry 2008; 64(12):1051-1059.

van den Oord EJCG, Kuo PH, Hartmann AM, Webb BT, Möller HJ, Hettema JM, Giegling I, Bukszár J, Rujescu D

Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism

Archives of general psychiatry 2008; 65(9):1062-1071.

Weickert CS, Miranda-Angulo AL, Wong J, Perlman WR, Ward SE, Radhakrishna V, Straub RE, Weinberger DR, Kleinman JE

Variants in the estrogen receptor alpha gene and its mRNA contribute to risk for schizophrenia

Human Molecular Genetics 2008; 17(15):2293-2309.

Duan J, Martinez M, Sanders AR, Hou C, Burrell GJ, Krasner AJ, Schwartz DB, Gejman PV

DTNBP1 (Dystrobrevin Binding Protein 1) and Schizophrenia: Association Evidence in the 3′ End of the Gene

Human Heredity 2007; 64(2):97-106.

Greenwood TA, Braff DL, Light GA, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RE, Gur RC

Initial heritability analyses of endophenotypic measures for schizophrenia: the consortium on the genetics of schizophrenia

Archives of general psychiatry 2007; 64(11):1242-1250.

Gur RE, Calkins ME, Gur RC, Horan WP, Nuechterlein KH, Seidman LJ, Stone WS

The Consortium on the Genetics of Schizophrenia: neurocognitive endophenotypes

Schizophr Bull 2007; 33(1):49-68.

Liu C, Shi J, Badner JA, Zou H, Qian Y, Gershon ES

No association of trace amine receptor genes with bipolar disorder

Mol Psychiatry 2007; 12(11):979-981.

Liu C-M, Liu Y-L, Fann S-J, Chen WJ, Yang W-C, Ouyang W-C, Chen C-Y, Jou Y-S, Hsieh M-H, Liu S-K, Hwang T-J, Faraone SV, Tsuang MT, Hwu H-G

Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families

Genes Brain Behav 2007; 6(6):497-502.

Liu C-M, Liu Y-L, Fann S-J, Yang W-C, Wu J-Y, Hung S-I, Chen WJ, Chueh C-M, Liu W-M, Liu C-C, Hsieh M-H, Hwang T-J, Faraone SV, Tsuang MT, Hwu H-G

No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families

Schizophr Res 2007; 93(1-3):391-398.

Liu YL, Fann CSJ, Liu CM, Chang CC, Yang WC, Hung SI, Yu SL, Hwang TJ, Hsieh MH, Liu CC, Tsuang MM, Wu JY, Jou YS, Faraone SV, Tsuang MT, Chen WJ, Hwu H-G

More evidence supports the association of PPP3CC with schizophrenia

Mol Psychiatry 2007; 1-9.

Meyer-Lindenberg A, Straub RE, Lipska BK, Verchinski BA, Goldberg T, Callicott JH, Egan MF, Huffaker SS, Mattay VS, Kolachana B, Kleinman JE, Weinberger DR

Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition

Journal of Clinical Investigation 2007; 117(3):672-682.

Philibert RA, Bohle P, Secrest D, Deaderick J, Sandhu H, Crowe R, Black DW

The association of the HOPA12bp polymorphism with schizophrenia in the NIMH genetics initiative for schizophrenia sample

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(6):743-747.

Radant AD, Dobie DJ, Calkins ME, Olincy A, Braff DL, Cadenhead KS, Freedman R, Green MF, Greenwood TA, Gur RE

Successful multi-site measurement of antisaccade performance deficits in schizophrenia

Schizophrenia research 2007; 89(1):320-329.

Saviouk V, Moreau MP, Tereshchenko IV, Brzustowicz LM

Association of Synapsin 2 with schizophrenia in families of Northern European ancestry

Schizophrenia research 2007; 96(1-3):100-111.

Straub RE, Lipska BK, Egan MF, Goldberg TE, Callicott JH, Mayhew MB, Vakkalanka RK, Kolachana BS, Kleinman JE, Weinberger DR

Allelic variation in GAD1 (GAD67) is associated with schizophrenia and influences cortical function and gene expression

Molecular psychiatry 2007; 12(9):854-869.

Turetsky BI, Calkins ME, Light GA, Olincy A, Radant AD, Swerdlow NR

Neurophysiological endophenotypes of schizophrenia: the viability of selected candidate measures

Schizophr Bull 2007; 33(1):69-94.

Faraone SV, Lasky-Su J, Glatt SJ, Eerdewegh PV, Tsuang MT

Early onset bipolar disorder: possible linkage to chromosome 9q34

Bipolar disorders 2006; 8(2):144-151.

Faraone SV, Hwu H-G, Liu C-M, Chen WJ, Tsuang M-M, Liu S-K, Shieh M-H, Hwang T-J, Ou-Yang W-C, Chen C-Y, Chen C-C, Lin J-J, Chou FH-C, Chueh C-M, Liu W-M, Hall M-H, Su J, Van Eerdewegh P, Tsuang MT

Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3

Am J Psychiatry 2006; 163:1760-1766.

Freedman R, Leonard S, Waldo M, Gault J, Olincy A, Adler LE

Characterization of allelic variants at chromosome 15q14 in schizophrenia

Genes, Brain and Behavior 2006; 5(S1):14-22.

Goldberg TE, Straub RE, Callicott JH, Hariri A, Mattay VS, Bigelow L, Coppola R, Egan MF, Weinberger DR

The G72/G30 gene complex and cognitive abnormalities in schizophrenia

Neuropsychopharmacology 2006; 31(9):2022-2032.

Liu Y-L, Fann CS-J, Liu C-M, Wu J-Y, Hung S-I, Chan H-Y, Chen J-J, Pan C-C, Liu S-K, Hsieh MH, Hwang T-J, OuYang W-C, Chen C-Y, Lin J-J, Chou FH-C, Chueh C-M, Liu W-M, Tsuang M-M, Faraone SV, Tsuang MT, Chen WJ, Hwu H-G

Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population

Psychiatr Genet 2006; 16:39-41.

Liu Y-L, Fann CS-J, Liu C-M, Wu J-Y, Hung S-I, Chan H-Y, Chen J-J, Lin C-Y, Liu S-K, Hsieh MH, Hwang T-J, OuYang W-C, Chen C-Y, Lin J-J, Chou FH-C, Chueh C-M, Liu W-M, Tsuang M-M, Faraone SV, Tsuang MT, Chen WJ, Hwu H-G

Evaluation of RGS4 as a candidate gene for schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2006; 141B:418-420.

Liu Y-L, Fann CS-J, Liu C-M, Chang C-C, Wu J-Y, Hung S-I, Liu S-K, Hsieh MH, Hwang T-J, Chan H-Y, Chen J-J, Faraone SV, Tsuang MT, Chen WJ, Hwu H-G

No association of G72 and D-amino acid oxidase genes with schizophrenia

Schizophr Res 2006; 87(1-3):15-20.

Mah S, Nelson MR, Delisi LE, Reneland RH, Markward N, James MR, Nyholt DR, Hayward N, Handoko H, Mowry B

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia

Molecular psychiatry 2006; 11(5):471-478.

Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV

Genomewide Linkage Scan of 409 European-Ancestry and African American Families with Schizophrenia: Suggestive Evidence of Linkage at 8p23

American Journal of Human Genetics 2006; 78(2):315-333.

Tosic M, Ott J, Barral S, Bovet P, Deppen P, Gheorghita F, Matthey ML, Parnas J, Preisig M, Saraga M

Schizophrenia and oxidative stress: glutamate cysteine ligase modifier as a susceptibility gene

The American Journal of Human Genetics 2006; 79(3):586-592.

Walss-Bass C, Montero AP, Armas R, Dassori A, Contreras SA, Liu W, Medina R, Levinson D, Pereira M, Atmella I

Linkage disequilibrium analyses in the Costa Rican population suggests discrete gene loci for schizophrenia at 8p23. 1 and 8q13. 3

Psychiatric genetics 2006; 16(4):159-168.

Bellivier F

Schizophrenia, antipsychotics and diabetes: genetic aspects

European psychiatry 2005; 20:S335-S339.

Brennan MD, Condra J

Transmission disequilibrium suggests a role for the sulfotransferase-4A1 gene in schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 139(1):69-72.

Corradi JP, Ravyn V, Robbins AK, Hagan KW, Bostwick R, Buono RJ, Berrettini WH, Furlong ST

Alternative transcripts and evidence of imprinting of GNAL on 18p11.2, a region linked to schizophrenia and bipolar disorder displaying parent-of-origin effects

Mol Psychiatry 2005; 10(11):1017-1025.

Duan J, Martinez M, Sanders AR, Hou C, Krasner AJ, Schwartz DB, Gejman PV

Neuregulin 1 (NRG1) and schizophrenia: analysis of a US family sample and the evidence in the balance

Psychological medicine 2005; 35(11):1599.

Holliday E, Mowry B, Chant D, Nyholt D

The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data

Human genetics 2005; 117(2-3):160-167.

Hwu H-G, Faraone SV, Liu C-M, Chen WJ, Liu S-K, Shieh M-H, Hwang T-J, Tsuang M-M, OuYang W-C, Chen C-Y, Chen C-C, Lin J-J, Chou FH-C, Chueh C-M, Liu W-M, Hall M-H, Tsuang MT

Taiwan schizophrenia linkage study: the field study

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2005; 134B:30-36.

Mulle JG, Chowdari KV, Nimgaonkar V, Chakravarti A

No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families

Molecular psychiatry 2005; 10(5):431-433.

Nurnberger JI

Meeting Report for Molecular Psychiatry, 2005

Psychiatric Genetics 2005; 15(4):241-242.

Prasad KM, Chowdari KV, Nimgaonkar VL, Talkowski ME, Lewis DA, Keshavan MS

Genetic polymorphisms of the RGS4 and dorsolateral prefrontal cortex morphometry among first episode schizophrenia patients

Mol Psychiatry 2005; 10:213-219.

Riley B, Kendler KS

Genetics of schizophrenia

Psychiatric genetics 2005; 95.

Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG, Wildenauer DB, Martinez M, Gejman PV

Haplotypic association spanning the 22q11. 21 genes COMT and ARVCF with schizophrenia

Molecular psychiatry 2005; 10(4):353-365.

Stopkova P, Vevera J, Paclt I, Zukov I, Papolos DF, Saito T, Lachman HM

Screening of PIP5K2A promoter region for mutations in bipolar disorder and schizophrenia

Psychiatric genetics 2005; 15(3):223-227.

Takahashi S, Faraone SV, Lasky-Su J, Tsuang MT

Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families

Psychiatry research 2005; 133(2):111-122.

Chen X, Dunham C, Kendler S, Wang X, O'Neill FA, Walsh D, Kendler KS

Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 129(1):23-26.

DeWan A, Ott J

Reanalysis of a genome scan for schizophrenia loci using multigenic methods

Human heredity 2004; 57(4):191-194.

Duan J, Martinez M, Sanders AR, Hou C, Saitou N, Kitano T, Mowry BJ, Crowe RR, Silverman JM, Levinson DF, Gejman PV

Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia

American Journal of Human Genetics 2004; 75(4):624-638.

Emamian ES, Hall D, Birnbaum MJ, Karayiorgou M, Gogos JA

Convergent evidence for impaired AKT1-GSK3β signaling in schizophrenia

Nature genetics 2004; 36(2):131-137.

Faraone SV, Su J, Taylor L, Wilcox M, Van Eerdewegh P, Tsuang MT

A novel permutation testing method implicates sixteen nicotinic acetylcholine receptor genes as risk factors for smoking in schizophrenia families

Human Heredity 2004; 57(2):59-68.

Iwamoto K, Bundo M, Washizuka S, Kakiuchi C, Kato T

Expression of HSPF1 and LIM in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia

Journal of human genetics 2004; 49(5):227-231.

Mowry BJ, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauche S

Multicenter linkage study of schizophrenia loci on chromosome 22q

Molecular psychiatry 2004; 9(8):784-795.

Berry N, Jobanputra V, Pal H

Molecular genetics of schizophrenia: a critical review

Journal of Psychiatry and Neuroscience 2003; 28(6):415-429.

Gault J, Hopkins J, Berger R, Drebing C, Logel J, Walton C, Short M, Vianzon R, Olincy A, Ross RG

Comparison of polymorphisms in the α7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 123(1):39-49.

Leonard S, Freedman R

Recombination in a schizophrenic proband fails to exclude CHRNA7 at chromosome 15q14.

Molecular psychiatry 2003; 8(2):.

Badner JA, Gershon ES

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

Molecular psychiatry 2002; 7(4):405-411.

Chao HM, Richardson MA

Aromatic amino acid hydroxylase genes and schizophrenia

American journal of medical genetics 2002; 114(6):626-630.

Curtis D, North BV, Sham PC

Extension of conditional model-free likelihood-based linkage analysis to additive and other models

Annals of human genetics 2002; 66(2):157-167.

DeLisi LE, Sherrington R, Shaw S, Nanthakumar B, Shields G, Smith AB, Wellman N, Larach NW, Loftus J, Razi K, Stewart J, Vita A, De Hurt M, Crow TJ, Sherrington R

A genome-wide scan of 382 affected sibling-pairs with schizophrenia suggests linkage to chromosomes 2cen and 10p

Am J Psychiatry 2002; 159:803-812.

Freedman R, Adler LE, Olincy A, Waldo MC, Ross RG, Stevens KE, Leonard S

Input dysfunction, schizotypy, and genetic models of schizophrenia

Schizophrenia research 2002; 54(1):25-32.

Leonard S, Gault J, Hopkins J, Logel J, Vianzon R, Short M, Drebing C, Berger R, Venn D, Sirota P, Zerbe G, Olincy A, Ross RG, Adler LE, Freedman R

Association of promoter variants in the α7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia

Arch Gen Psychiatry 2002; 59:1085-1096.

Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV, Schwab SG, Williams NM, Owen MJ, Wildenauer DB, Sanders AR, Nestadt G, Mowry BJ, Wormley B, Bauche S, Soubigou S, Ribble R, Nertney DA, Liang KY, Martinolich L, Maier W, Norton N, Williams H, Albus M, Carpenter EB, deMarchi N, Ewen-White KR, Walsh D, Jay M, Deleuze J-F, O'Neill FA, Papadimitriou G, Weilbaecher A, Lerer B, O'Donovan MC, Dikeos D, Silverman JM, Kendler KS, Mallet J, Crowe RR, Walters M

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

Science 2002; 296:739-741.

Liu H, Heath SC, Sobin C, Roos JL, Galke BL, Blundell ML, Lenane M, Robertson B, Wijsman EM, Rapoport JL, Gogos JA, Karayiorgou M

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Proceedings of the National Academy of Sciences of the United States of America 2002; 99(6):3717-3722.

Sklar P

Linkage analysis in psychiatric disorders: the emerging picture

Annual review of genomics and human genetics 2002; 3(1):371-413.

Waterworth DM, Bassett AS, Brzustowicz LM

Recent advances in the genetics of schizophrenia

Cellular and molecular life sciences : CMLS 2002; 59(2):331-348.

Freedman R, Leonard S, Gault JM, Hopkins J, Cloninger CR, Kaufmann CA, Tsuang MT, Farone SV, Malaspina D, Svrakic DM

Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the α7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

American journal of medical genetics 2001; 105(1):20-22.

Nurnberger Jr JI

Park City, Utah Molecular Psychiatry Meeting, February 2001

Psychiatric genetics 2001; 11(1):1-4.

Sanders AR, Cao Q, Taylor J, Levin TE, Badner JA, Cravchik A, Comeron JM, Naruya S, Del Rosario A, Salvi DA

Genetic diversity of the human serotonin receptor 1B (HTR1B) gene

Genomics 2001; 72(1):1-14.

Freedman R, Adams CE, Adler LE, Bickford PC, Gault J, Harris JG, Nagamoto HT, Olincy A, Ross RG, Stevens KE

Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophrenia

American journal of medical genetics 2000; 97(1):58-64.

Riley BP, McGuffin P

Linkage and associated studies of schizophrenia

American journal of medical genetics 2000; 97(1):23-44.

DeLisi LE

A critical overview of recent investigations into the genetics of schizophrenia

Current opinion in Psychiatry 1999; 12(1):29-39.

Faraone SV, Meyer J, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B, Hampe C, Chan G, Aelony A

Brief Research Communication Suggestive Linkage of Chromosome 10p to Schizophrenia Is Not Due to Transmission Ratio Distortion

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1999; 88(6):607-608.

Freedman R, Adler LE, Leonard S

Alternative phenotypes for the complex genetics of schizophrenia

Biological psychiatry 1999; 45(5):551-558.

Harkavy-Friedman JM, Restifo K, Malaspina D, Kaufmann CA, Amador XF, Yale SA, Gorman JM

Suicidal behavior in schizophrenia: characteristics of individuals who had and had not attempted suicide

American Journal of Psychiatry 1999

Levinson DF, Mowry BJ

4 Genetics of Schizophrenia

Genetic influences on neural and behavioral functions 1999; 47.

Maier W, Rietschel M, Lichtermann D, Wildenauer DB

Family and genetic studies on the relationship of schizophrenia to affective disorders

European archives of psychiatry and clinical neuroscience 1999; 249(4):S57-S61.

Martinez M, Goldin LR, Cao Q, Zhang J, Sanders AR, Nancarrow DJ, Taylor JM, Levinson DF, Kirby A, Crowe RR

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

American journal of medical genetics 1999; 88(4):337-343.

Cloninger CR, Kaufmann CA, Faraone SV, Malaspina D, Syrakic DM, Harkavy-Friedman J, Suarez BK, Matise TC, Shore D, Lee H, Hampe CL, Wynne D, Drain C, Markel PD, Zambuto CT, Schmitt K, Tsuang MT

Genome-wide search for schizophrenia susceptibility loci:The NIMH Genetics Initiative and Millennium Consortium

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:275-281.

Faraone SV, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B, Hampe C, Zambuto CT, Schmitt K, Meyer J, Markel P, Lee H, Harkavy-Friedman J, Kaufmann C, Cloninger CR, Tsuang MT

Genome scan of European-American schizophrenia pedigrees: Results of the NIMH Genetics Initiative and Millennium Consortium

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:290-295.

Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto CT, Schmitt K, Matise TC

NIMH Genetics Initiative Millennium Schizophrenia Consortium: Linkage Analysis of

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:282-289.

Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto CT, Schmitt K, Matise TC, Harkavy-Friedman JM, Hampe C, Lee H, Shore D, Wynne D, Faraone SV, Tsuang MT, Cloninger R, NIMH Genetics Initiative Millennium Schizophrenia Consortium

Linkage analysis of African-American pedigrees

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:282-289.

Leonard S, Gault J, Moore T, Hopkins J, Robinson M, Oliney A, Adler LE, Cloninger CR, Kaufmann CA, Tsuang MT, Faraone SV, Malaspina D, Svrakic DM, Freedman R

Further investigation of a chromosome 15 locus in schizophrenia: Analysis of affected sibpairs from the NIMH Genetics Initiative

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:308-312.

Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D

Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis

American journal of medical genetics 1998; 81(4):302-307.

Shaw S, Sherrington R, Cardon L, Smith A, Shields G, Loftus J, Vita A, Crow TJ, DeLisi LE

A genome-wide screen for linkage to schizophrenia

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81:364-376.

Cao Q, Martinez M, Zhang J, Sanders AR, Badner JA, Cravchik A, Markey CJ, Beshah E, Guroff JJ, Maxwell ME

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

Genomics 1997; 43(1):1-8.

Johnson JE, Cleary J, Ahsan H, Harkavy Friedman J, Malaspina D, Cloninger CR, Faraone SV, Tsuang MT, Kaufmann CA

Anticipation in schizophrenia: biology or bias?

American journal of medical genetics 1997; 74(3):275-280.

Blehar MC, Faraone SV, Zeller PJ, Nurnberger JI, Tsuang MT, Kirch DG, Shore D, Gershefski JMA, Reich T, Cloninger CR, Rau NL, DePaulo JR, Kaufmann CA, Harkavy-Friedman J, Malaspina D, Weise RE

Differentiation of schizoaffective bipolar disorder from bipolar disorder and schizophrenia

Depression 1996; 3(6):309-315.

Faraone SV, Blehar M, Pepple J, Moldin SO, Norton J, Nurnberger JI, Malaspina D, Kaufmann CA, Reich T, Cloninger CR

Diagnostic accuracy and confusability analyses: an application to the Diagnostic Interview for Genetic Studies

Psychological medicine 1996; 26(02):401-410.

Stewart L, Hall AL, Kang SHL, Shaw CA, Beaudet AL

Supplemental Methods

Fear and Anxiety

Lee M, Aggen SH, Otowa T, Castelao E, Preisig M, Grabe HJ, Hartman CA, Oldehinkel AJ, Middeldorp CM, Tiemeier H, Hettema JM

Assessment and Characterization of Phenotypic Heterogeneity of Anxiety Disorders across Five Large Cohorts

International journal of methods in psychiatric research 2016; 25(4):255-266.

Kerner B, Rao AR, Christensen B, Dandekar S, Yourshaw M, Nelson SF

Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways

Frontiers in Psychiatry 2013; 4:154.

Hettema JM, Webb BT, Guo AY, Zhao Z, Maher BS, Chen X, An SS, Sun C, Aggen SH, Kendler KS, Kuo PH, Otowa T, Flint J, van den Oord EJ

Prioritization and Association Analysis of Murine-Derived Candidate Genes in Anxiety-Spectrum Disorders

Biological psychiatry 2011; 70(9):888-896.

Strug LJ, Suresh R, Fyer A, Talati A, Adams PB, Li W, Hodge SE, Gilliam TC, Weissman MM

Panic Disorder is Associated with the Serotonin Transporter Gene (SLC6A4) But Not the Promoter Region (5-HTTLPR)

Molecular psychiatry 2010; 15(2):166-176.

Krishnan KRR

Psychiatric and medical comorbidities of bipolar disorder

Psychosomatic medicine 2005; 67(1):1-8.

Post Traumatic Stress Disorder

Stein Murray B, Chen Chia-Yen, Ursano Robert J, Cai Tianxi, Gelernter Joel, Heeringa Steven G, Jain Sonia, Jensen Kevin P, Maihofer Adam X, Mitchell Colter, Nievergelt Caroline M, Nock Matthew K, Neale Benjamin M, Polimanti Renato, Ripke Stephan, Sun Xiaoying, Thomas Michael L, Wang Qian, Ware Erin B, Borja Susan, Kessler Ronald C, Smoller Jordan W

Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers.

JAMA psychiatry 2016; 73(7):695-704.

Suicide

William N, Reissner C, Sargent R, Darlington TM, DiBlasi E, Li QS, Keeshin B, Callor WB, Ferris E, Jerominski L, Smith KR, Christensen ED, Gray DM, Camp NJ, Missler M, Williams ME, Coon H

Neurexin 1 Variants as Risk Factors for Suicide Death

Molecular psychiatry 2021; 26(12):7436-7445.

Coon H, Darlington TM, DiBlasi E, Callor WB, Ferris E, Fraser A, Yu Z, William N, Das SC, Crowell SE, Chen D, Anderson JS, Klein M, Jerominski L, Cannon D, Shabalin A, Docherty A, Williams M, Smith KR, Keeshin B, Bakian AV, Christensen E, Li QS, Camp NJ, Gray D

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

Molecular psychiatry 2018; 10.1038/s41380-018-0282-3.

Monson ET, Pirooznia M, Parla J, Kramer M, Goes FS, Gaine ME, Gaynor SC, de Klerk K, Jancic D, Karchin R, McCombie WR, Zandi PP, Potash JB, Willour VL

Assessment of Whole-Exome Sequence Data in Attempted Suicide within a Bipolar Disorder Cohort

Molecular Neuropsychiatry 2017; 3(1):1-11.

Breen ME, Gaynor SC, Monson ET, de Klerk K, Parsons MG, Braun TA, DeLuca AP, Zandi PP, Potash JB, Willour VL

Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder

PLoS ONE 2016; 11(12):e0169158.

Mann JJ, Arango VA, Avenevoli S, Brent DA, Champagne FA, Clayton P, Currier D, Dougherty DM, Haghighi F, Hodge SE

Candidate endophenotypes for genetic studies of suicidal behavior

Biological psychiatry 2009; 65(7):556-563.

Lopez VA, Detera-Wadleigh S, Cardona I, Kassem L, McMahon FJ, National Institute of Mental Health Genetics Initiative Bipolar Disorder Consortium

Nested association between genetic variation in tryptophan hydroxylase II, bipolar affective disorder, and suicide attempts

Biological psychiatry 2007; 61(2):181-186.

Velocardiofacial Syndrome

Gokhale A, Hartwig C, Freeman AA, Bassell JL, Zlatic SA, Sapp Savas C, Vadlamudi T, Abudulai F, Pham TT, Crocker A, Werner E, Wen Z, Repetto GM, Gogos JA, Claypool SM, Forsyth JK, Bearden CE, Glausier J, Lewis DA, Seyfried NT, Kwong JQ, Faundez V

Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior

The Journal of Neuroscience 2019; 39(18):3561-3581.

PsychENCODE Consortium

Li S, Li J, Liu J, Wang J, Li X, Huo Y, Li Y, Liu Y, Li M, Xiao X, Luo XJ

Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression

Brain 2021; 145(2):770-786.

Jiang Y, Giase G, Grennan K, Shieh AW, Xia Y, Han L, Wang Q, Wei Q, Chen R, Liu S, White KP, Chen C, Li B, Liu C

DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data

PLoS Computational Biology 2020; 16(4):e1007522.

Li W, Cai X, Li HJ, Song M, Zhang CY, Yang Y, Zhang L, Zhao L, Liu W, Wang L, Shao M, Zhang Y, Zhang C, Cai J, Zhou DS, Li X, Hui L, Jia QF, Qu N, Zhong BL, Zhang SF, Chen J, Xia B, Li Y, Song X, Fan W, Tang W, Tang W, Tang J, Chen X, Yue W, Zhang D, Fang Y, Xiao X, Li M, Lv L, Chang H

Independent replications and integrative analyses confirm TRANK1 as a susceptibility gene for bipolar disorder

Neuropsychopharmacology 2020; 46(6):1103-1112.

Li HJ, Qu N, Hui L, Cai X, Zhang CY, Zhong BL, Zhang SF, Chen J, Xia B, Wang L, Jia QF, Li W, Chang H, Xiao X, Li M, Li Y

Further confirmation of netrin 1 receptor (DCC) as a depression risk gene via integrations of multi-omics data

Translational Psychiatry 2020; 10:98.

Sey NY, Hu B, Mah W, Fauni H, McAfee JC, Rajarajan P, Brennand KJ, Akbarian S, Won H

A computational tool (H-MAGMA) for improved prediction of brain disorder risk genes by incorporating brain chromatin interaction profiles

Nature neuroscience 2020; 23(4):583-593.

Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AM, Tebbenkamp AT, Kaur N, Gulden FO, Breen MS, Liang L, Gilson MC, Zhao X, Dong S, Klei L, Cicek AE, Buxbaum JD, Adle-Biassette H, Thomas JL, Aldinger KA, O'Day DR, Glass IA, Zaitlen NA, Talkowski ME, Roeder K, State MW, Devlin B, Sanders SJ, Sestan N

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

Cell reports 2020; 31(1):107489.

Liu W, Yan H, Zhou D, Cai X, Zhang Y, Li S, Li H, Li S, Zhou DS, Li X, Zhang C, Sun Y, Dai JP, Zhong J, Yao YG, Luo XJ, Fang Y, Zhang D, Ma Y, Yue W, Li M, Xiao X

The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population

Translational Psychiatry 2019; 9:333.

Ning Z, Williams JM, Kumari R, Baranov PV, Moore T

Opposite Expression Patterns of Spry3 and p75NTR in Cerebellar Vermis Suggest a Male-Specific Mechanism of Autism Pathogenesis

Frontiers in Psychiatry 2019; 10:416.

Price AJ, Collado-Torres L, Ivanov NA, Xia W, Burke EE, Shin JH, Tao R, Ma L, Jia Y, Hyde TM, Kleinman JE, Weinberger DR, Jaffe AE

Divergent neuronal DNA methylation patterns across human cortical development reveal critical periods and a unique role of CpH methylation

Genome Biology 2019; 20:196.

Vawter MP, Schulmann A, Alhassen L, Alhassen W, Hamzeh AR, Sakr J, Pauluk L, Yoshimura R, Wang X, Dai Q, Sanathara N, Civelli O, Alachkar A

Melanin Concentrating Hormone Signaling Deficits in Schizophrenia: Association With Memory and Social Impairments and Abnormal Sensorimotor Gating

International Journal of Neuropsychopharmacology 2019; 23(1):53-65.

Walker RL, Ramaswami G, Hartl C, Mancuso N, Gandal MJ, de la Torre-Ubieta L, Pasaniuc B, Stein JL, Geschwind DH

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms

Cell 2019; 179(3):750-771.e22.

Amiri Anahita, Coppola Gianfilippo, Scuderi Soraya, Wu Feinan, Roychowdhury Tanmoy, Liu Fuchen, Pochareddy Sirisha, Shin Yurae, Safi Alexias, Song Lingyun, Zhu Ying, Sousa Andre M. M., Gerstein Mark, Crawford Gregory E., Sestan Nenad, Abyzov Alexej, Vaccarino Flora M.

Transcriptome and epigenome landscape of human cortical development modeled in organoids

Science 2018; 362(6420):.

Amiri A, Coppola G, Scuderi S, Wu F, Roychowdhury T, Liu F, Pochareddy S, Shin Y, Safi A, Song L, Zhu Y, Sousa AM, Gerstein M, Crawford GE, Sestan N, Abyzov A, Vaccarino FM

Transcriptome and epigenome landscape of human cortical development modeled in brain organoids

Science (New York, N.Y.) 2018; 362(6420):eaat6720.

An Joon-Yong, Lin Kevin, Zhu Lingxue, Werling Donna M., Dong Shan, Brand Harrison, Wang Harold Z., Zhao Xuefang, Schwartz Grace B., Collins Ryan L., Currall Benjamin B., Dastmalchi Claudia, Dea Jeanselle, Duhn Clif, Gilson Michael C., Klei Lambertus, Liang Lindsay, Markenscoff-Papadimitriou Eirene, Pochareddy Sirisha, Ahituv Nadav, Buxbaum Joseph D., Coon Hilary, Daly Mark J., Kim Young Shin, Marth Gabor T., Neale Benjamin M., Quinlan Aaron R., Rubenstein John L., Sestan Nenad, State Matthew W., Willsey A. Jeremy, Talkowski Michael E., Devlin Bernie, Roeder Kathryn, Sanders Stephan J.

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Science 2018; 362(6420):.

An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, Klei L, Liang L, Markenscoff-Papadimitriou E, Pochareddy S, Ahituv N, Buxbaum JD, Coon H, Daly MJ, Kim YS, Marth GT, Neale BM, Quinlan AR, Rubenstein JL, Sestan N, State MW, Willsey AJ, Talkowski ME, Devlin B, Roeder K, Sanders SJ

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Science (New York, N.Y.) 2018; 362(6420):eaat6576.

Chen Chao, Meng Qingtuan, Xia Yan, Ding Chaodong, Wang Le, Dai Rujia, Cheng Lijun, Gunaratne Preethi, Gibbs Richard A., Min Shishi, Coarfa Cristian, Reid Jeffrey G., Zhang Chunling, Jiao Chuan, Jiang Yi, Giase Gina, Thomas Amber, Fitzgerald Dominic, Brunetti Tonya, Shieh Annie, Xia Cuihua, Wang Yongjun, Wang Yunpeng, Badner Judith A., Gershon Elliot S., White Kevin P., Liu Chunyu

The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders

Science Translational Medicine 2018

Chen C, Meng Q, Xia Y, Ding C, Wang L, Dai R, Cheng L, Gunaratne P, Gibbs RA, Min S, Coarfa C, Reid JG, Zhang C, Jiao C, Jiang Y, Giase G, Thomas A, Fitzgerald D, Brunetti T, Shieh A, Xia C, Wang Y, Wang Y, Badner JA, Gershon ES, White KP, Liu C

POU3F2 is a regulator of a gene coexpression network in brain tissue from patients with neuropsychiatric disorders

Science translational medicine 2018; 10(472):eaat8178.

de la Torre Ubieta L, Stein JL, Won H, Opland CK, Liang D, Lu D, Geschwind DH

The dynamic landscape of open chromatin during human cortical neurogenesis

Cell 2018; 172(1-2):289-304.e18.

Dong X, Liao Z, Gritsch D, Hadzhiev Y, Bai Y, Locascio JJ, Guennewig B, Liu G, Blauwendraat C, Wang T, Adler CH, Hedreen JC, Faull RL, Frosch MP, Nelson PT, Rizzu P, Cooper AA, Heutink P, Beach TG, Mattick JS, Müller F, Scherzer CR

Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease

Nature neuroscience 2018; 21(10):1482-1492.

Finucane HK, Reshef YA, Anttila V, Slowikowski K, Gusev A, Byrnes A, Gazal S, Loh PR, Lareau C, Shoresh N, Genovese G, Saunders A, Macosko E, Pollack S, Perry JR, Buenrostro JD, Bernstein BE, Raychaudhuri S, McCarroll S, Neale BM, Price AL

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

Nature genetics 2018; 50(4):621-629.

Gandal Michael J., Zhang Pan, Hadjimichael Evi, Walker Rebecca L., Chen Chao, Liu Shuang, Won Hyejung, van Bakel Harm, Varghese Merina, Wang Yongjun, Shieh Annie W., Haney Jillian, Parhami Sepideh, Belmont Judson, Kim Minsoo, Moran Losada Patricia, Khan Zenab, Mleczko Justyna, Xia Yan, Dai Rujia, Wang Daifeng, Yang Yucheng T., Xu Min, Fish Kenneth, Hof Patrick R., Warrell Jonathan, Fitzgerald Dominic, White Kevin, Jaffe Andrew E., Peters Mette A., Gerstein Mark, Liu Chunyu, Iakoucheva Lilia M., Pinto Dalila, Geschwind Daniel H.

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Science 2018; 362(6420):.

Gandal MJ, Zhang P, Hadjimichael E, Walker RL, Chen C, Liu S, Won H, van Bakel H, Varghese M, Wang Y, Shieh AW, Haney J, Parhami S, Belmont J, Kim M, Losada PM, Khan Z, Mleczko J, Xia Y, Dai R, Wang D, Yang YT, Xu M, Fish K, Hof PR, Warrell J, Fitzgerald D, White K, Jaffe AE, Peters MA, Gerstein M, Liu C, Iakoucheva LM, Pinto D, Geschwind DH

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Science (New York, N.Y.) 2018; 362(6420):eaat8127.

Gandal MJ, Haney JR, Parikshak NN, Leppa V, Ramaswami G, Hartl C, Schork AJ, Appadurai V, Buil A, Werge TM, Liu C, White KP, Horvath S, Geschwind DH

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

Science (New York, N.Y.) 2018; 359(6376):693-697.

Girdhar K, Hoffman GE, Jiang Y, Brown L, Kundakovic M, Hauberg ME, Francoeur NJ, Wang YC, Shah H, Kavanagh DH, Zharovsky E, Jacobov R, Wiseman JR, Park R, Johnson JS, Kassim BS, Sloofman L, Mattei E, Weng Z, Sieberts SK, Peters MA, Harris BT, Lipska BK, Sklar P, Roussos P, Akbarian S

Cell-specific histone modification maps link schizophrenia risk to the neuronal epigenome

Nature neuroscience 2018; 21(8):1126-1136.

Gusev A, Mancuso N, Won H, Kousi M, Finucane HK, Reshef Y, Song L, Safi A, McCarroll S, Neale B, Ophoff RA, O'Donovan MC, Crawford GE, Geschwind DH, Katsanis N, Sullivan PF, Pasaniuc B, Price AL

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Nature genetics 2018; 50(4):538-548.

Kozlenkov A, Li J, Apontes P, Hurd YL, Byne WM, Koonin EV, Wegner M, Mukamel EA, Dracheva S

A unique role for DNA (hydroxy)methylation in epigenetic regulation of human inhibitory neurons

Science Advances 2018; 4(9):eaau6190.

Li Mingfeng, Santpere Gabriel, Imamura Kawasawa Yuka, Evgrafov Oleg V., Gulden Forrest O., Pochareddy Sirisha, Sunkin Susan M., Li Zhen, Shin Yurae, Zhu Ying, Sousa Andr'e M. M., Werling Donna M., Kitchen Robert R., Kang Hyo Jung, Pletikos Mihovil, Choi Jinmyung, Muchnik Sydney, Xu Xuming, Wang Daifeng, Lorente-Galdos Belen, Liu Shuang, Giusti-Rodr'iguez Paola, Won Hyejung, de~Leeuw Christiaan A., Pardinas Antonio F., Hu Ming, Jin Fulai, Li Yun, Owen Michael J., O'Donovan Michael C., Walters James T. R., Posthuma Danielle, Levitt Pat, Weinberger Daniel R., Hyde Thomas M., Kleinman Joel E., Geschwind Daniel H., Hawrylycz Michael J., State Matthew W., Sanders Stephan J., Sullivan Patrick F., Gerstein Mark B., Lein Ed S., Knowles James A., Sestan Nenad

Integrative Functional Genomic Analysis of Human Brain Development and Neuropsychiatric Risk

Science 2018; 362(6420):.

Meng Qingtuan, Wang Kangli, Brunetti Tonya, Xia Yan, Jiao Chuan, Dai Rujia, Fitzgerald Dominic, Thomas Amber, Jay Lindsey, Eckart Heather, Grennan Kay, Imamura-Kawasawa Yuka, Li Mingfeng, Sestan Nenad, White Kevin P., Chen Chao, Liu Chunyu

The DGCR5 long noncoding RNA may regulate expression of several schizophrenia-related genes

Science Translational Medicine 2018

Meng Q, Wang K, Brunetti T, Xia Y, Jiao C, Dai R, Fitzgerald D, Thomas A, Jay L, Eckart H, Grennan K, Imamura-Kawasawa Y, Li M, Sestan N, White KP, Chen C, Liu C

A Long Non-coding RNA DGCR5 May Contribute to Regulating Expression of Schizophrenia-Related Genes

Science translational medicine 2018; 10(472):eaat6912.

Rajarajan Prashanth, Borrman Tyler, Liao Will, Schrode Nadine, Flaherty Erin, Casino Charlize, Powell Samuel, Yashaswini Chittampalli, LaMarca Elizabeth A., Kassim Bibi, Javidfar Behnam, Espeso-Gil Sergio, Li Aiqun, Won Hyejung, Geschwind Daniel H., Ho Seok-Man, MacDonald Matthew, Hoffman Gabriel E., Roussos Panos, Zhang Bin, Hahn Chang-Gyu, Weng Zhiping, Brennand Kristen J., Akbarian Schahram

Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk

Science 2018; 362(6420):.

Rhie Suhn K., Schreiner Shannon, Witt Heather, Armoskus Chris, Lay Fides D., Camarena Adrian, Spitsyna Valeria N., Guo Yu, Berman Benjamin P., Evgrafov Oleg V., Knowles James A., Farnham Peggy J.

Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation

Science Advances 2018; 4(12):.

Rhie SK, Schreiner S, Witt H, Armoskus C, Lay FD, Camarena A, Spitsyna VN, Guo Y, Berman BP, Evgrafov OV, Knowles JA, Farnham PJ

Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation

Science Advances 2018; 4(12):eaav8550.

Rhie SK, Schreiner S, Farnham PJ

Defining Regulatory Elements in the Human Genome Using Nucleosome Occupancy and Methylome Sequencing (NOMe-seq)

Methods in molecular biology (Clifton, N.J.) 2018; 1766:209-229.

Toker L, Mancarci BO, Tripathy S, Pavlidis P

Transcriptomic evidence for alterations in astrocytes and parvalbumin interneurons in bipolar disorder and schizophrenia subjects

Biological psychiatry 2018; 84(11):787-796.

Wang Daifeng, Liu Shuang, Warrell Jonathan, Won Hyejung, Shi Xu, Navarro Fabio C. P., Clarke Declan, Gu Mengting, Emani Prashant, Yang Yucheng T., Xu Min, Gandal Michael J., Lou Shaoke, Zhang Jing, Park Jonathan J., Yan Chengfei, Rhie Suhn Kyong, Manakongtreecheep Kasidet, Zhou Holly, Nathan Aparna, Peters Mette, Mattei Eugenio, Fitzgerald Dominic, Brunetti Tonya, Moore Jill, Jiang Yan, Girdhar Kiran, Hoffman Gabriel E., Kalayci Selim, Gumus Zeynep H., Crawford Gregory E., Roussos Panos, Akbarian Schahram, Jaffe Andrew E., White Kevin P., Weng Zhiping, Sestan Nenad, Geschwind Daniel H., Knowles James A., Gerstein Mark B.

Comprehensive functional genomic resource and integrative model for the human brain

Science 2018; 362(6420):.

Wang D, Liu S, Warrell J, Won H, Shi X, Navarro FC, Clarke D, Gu M, Emani P, Yang YT, Xu M, Gandal MJ, Lou S, Zhang J, Park JJ, Yan C, Rhie SK, Manakongtreecheep K, Zhou H, Nathan A, Peters M, Mattei E, Fitzgerald D, Brunetti T, Moore J, Jiang Y, Girdhar K, Hoffman GE, Kalayci S, Gümüş ZH, Crawford GE, Roussos P, Akbarian S, Jaffe AE, White KP, Weng Z, Sestan N, Geschwind DH, Knowles JA, Gerstein MB

Comprehensive functional genomic resource and integrative model for the human brain

Science (New York, N.Y.) 2018; 362(6420):eaat8464.

Zhu Ying, Sousa Andre M. M., Gao Tianliuyun, Skarica Mario, Li Mingfeng, Santpere Gabriel, Esteller-Cucala Paula, Juan David, Ferrandez-Peral Luis, Gulden Forrest O., Yang Mo, Miller Daniel J., Marques-Bonet Tomas, Imamura Kawasawa Yuka, Zhao Hongyu, Sestan Nenad

Spatiotemporal transcriptomic divergence across human and macaque brain development

Science 2018; 362(6420):.

Zhu Y, Sousa AM, Gao T, Skarica M, Li M, Santpere G, Esteller-Cucala P, Juan D, Ferrández-Peral L, Yang M, Miller DJ, Marques-Bonet T, Kawasawa YI, Zhao H, Sestan N

Spatio-temporal transcriptomic divergence across human and macaque brain development

Science (New York, N.Y.) 2018; 362(6420):eaat8077.

Carlyle BC, Kitchen RR, Kanyo JE, Voss EZ, Pletikos M, Sousa AM, Lam TT, Gerstein MB, Sestan N, Nairn AC

A Multiregional Proteomic Survey of the Postnatal Human Brain

Nature neuroscience 2017; 20(12):1787-1795.

Sousa AM, Zhu Y, Raghanti MA, Kitchen RR, Onorati M, Tebbenkamp AT, Stutz B, Meyer KA, Li M, Kawasawa YI, Liu F, Perez RG, Mele M, Carvalho T, Skarica M, Gulden FO, Pletikos M, Shibata A, Stephenson AR, Edler MK, Ely JJ, Elsworth JD, Horvath TL, Hof PR, Hyde TM, Kleinman JE, Weinberger DR, Reimers M, Lifton RP, Mane SM, Noonan JP, State MW, Lein ES, Knowles JA, Marques-Bonet T, Sherwood CC, Gerstein MB, Sestan N

Molecular and Cellular Reorganization of Neural Circuits in the Human Lineage

Science (New York, N.Y.) 2017; 358(6366):1027-1032.

Akbarian S, Liu C, Knowles JA, Vaccarino FM, Farnham PJ, Crawford GE, Jaffe AE, Pinto D, Dracheva S, Geschwind DH

The PsychENCODE project

Nature neuroscience 2015; 18(12):1707-1712.

Tourette Syndrome

Abdulkadir M, Yu D, Osiecki L, King RA, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, Garcia-Delgar B, Gilbert DL, Grice DE, Hagstrøm J, Hedderly T, Heyman I, Hong HJ, Huyser C, Ibanez-Gomez L, Kim YK, Kim YS, Koh YJ, Kook S, Kuperman S, Leventhal B, Madruga-Garrido M, Maras A, Mir P, Morer A, Münchau A, Plessen KJ, Roessner V, Shin EY, Song DH, Song J, Visscher F, Zinner SH, Mathews CA, Scharf JM, Tischfield JA, Heiman GA, Dietrich A, Hoekstra PJ

Investigation of gene-environment interactions in relation to tic severity

Journal of neural transmission (Vienna, Austria : 1996) 2021; 128(11):1757-1765.

Cao X, Zhang Y, Abdulkadir M, Deng L, Fernandez TV, Garcia-Delgar B, Hagstrøm J, Hoekstra PJ, King RA, Koesterich J, Kuperman S, Morer A, Nasello C, Plessen KJ, Thackray JK, Zhou L, Dietrich A, Tischfield JA, Heiman GA, Xing J

Whole exome sequencing identifies genes associated with Tourette's Disorder in multiplex families

Molecular psychiatry 2021; 26(11):6937-6951.

Sun N, Nasello C, Deng L, Wang N, Zhang Y, Xu Z, Song Z, Kwan K, King R A, Pang Z P, Xing J, Heiman G A, Tischfield J A

The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.

Molecular psychiatry 2018; 23(6):1487-1495.

Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, Khalifa N, Dahl N, Huang AY, Neale BM, Coppola G, Mathews CA, Fernandez TV, Buxbaum JD, De Rubeis S, Grice DE, Xing J, Heiman GA, Tischfield JA, Paschou P, Willsey AJ, State MW

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Cell reports 2018; 24(13):3441-3454.e12.

Abdulkadir M, Londono D, Gordon D, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, Elzerman L, Fremer C, Fründt O, Garcia-Delgar B, Gilbert DL, Grice DE, Hedderly T, Heyman I, Hong HJ, Huyser C, Ibanez-Gomez L, Jakubovski E, Kim YK, Kim YS, Koh YJ, Kook S, Kuperman S, Leventhal B, Ludolph AG, Madruga-Garrido M, Maras A, Mir P, Morer A, Müller-Vahl K, Münchau A, Murphy TL, Plessen KJ, Roessner V, Shin EY, Song DH, Song J, Tübing J, van den Ban E, Visscher F, Wanderer S, Woods M, Zinner SH, King RA, Tischfield JA, Heiman GA, Hoekstra PJ, Dietrich A

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

European Archives of Psychiatry and Clinical Neuroscience 2017; 268(3):301-316.

Willsey AJ, Fernandez TV, Yu D, King RA, Dietrich A, Xing J, Sanders SJ, Mandell JD, Huang AY, Richer P, Smith L, Dong S, Samocha KE, Neale BM, Coppola G, Mathews CA, Tischfield JA, Scharf JM, State MW, Heiman GA

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Neuron 2017; 94(3):486-499.e9.

Huertas-Fernández Ismael, Gómez-Garre Pilar, Madruga-Garrido Marcos, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Martín-Rodríguez Juan Francisco, Cáceres-Redondo María Teresa, Vargas-González Laura, Carrillo Fátima, Pascual Alberto, Tischfield Jay A, King Robert A, Heiman Gary A, Mir Pablo

GDNF gene is associated with tourette syndrome in a family study.

Movement disorders : official journal of the Movement Disorder Society 2015; 30(8):1115-20.

Scharf J M, Yu D, Mathews C A, Neale B M, Stewart S E, Fagerness J A, Evans P, Gamazon E, Edlund C K, Service S K, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis L K, Han B, Crane J, Moorjani P, Crenshaw A T, Parkin M A, Reus V I, Lowe T L, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath D C, Smit J H, King R A, Fernandez T V, Leckman J F, Kidd K K, Kidd J R, Pakstis A J, State M W, Herrera L D, Romero R, Fournier E, Sandor P, Barr C L, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman C L, Bruun R D, Erenberg G, Naarden A L, Lee P C, Weiss N, Kremeyer B, Berrío G B, Campbell D D, Cardona Silgado J C, Ochoa W C, Mesa Restrepo S C, Muller H, Valencia Duarte A V, Lyon G J, Leppert M, Morgan J, Weiss R, Grados M A, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield J A, Heiman G A, Gilbert D L, Hoekstra P J, Robertson M M, Kurlan R, Liu C, Gibbs J R, Singleton A, Hardy J, Strengman E, Ophoff R A, Wagner M, Moessner R, Mirel D B, Posthuma D, Sabatti C, Eskin E, Conti D V, Knowles J A, Ruiz-Linares A, Rouleau G A, Purcell S, Heutink P, Oostra B A, McMahon W M, Freimer N B, Cox N J, Pauls D L

Genome-wide association study of Tourette's syndrome.

Molecular psychiatry 2013; 18(6):721-8.

Uncategorized

Konte B, Walters JT, Rujescu D, Legge SE, Pardiñas AF, Cohen D, Pirmohamed M, Tiihonen J, Hartmann AM, Bogers JP, van der Weide J, van der Weide K, Putkonen A, Repo-Tiihonen E, Hallikainen T, Silva E, Ingimarsson O, Sigurdsson E, Kennedy JL, Sullivan PF, Rietschel M, Breen G, Stefansson H, Stefansson K, Collier DA, O'Donovan MC, Giegling I

HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry

Translational Psychiatry 2021; 11:214.

Alexander-Bloch AF, Raznahan A, Vandekar SN, Seidlitz J, Lu Z, Matthias SR, Knowles E, Mollon J, Rodrigue A, Curran JE, Görring HH, Satterthwaite TD, Gur RE, Bassett DS, Hoftman GD, Pearlson G, Shinohara RT, Liu S, Fox PT, Almasy L, Blangero J, Glahn DC

Imaging local genetic influences on cortical folding

Proceedings of the National Academy of Sciences of the United States of America 2020; 117(13):7430-7436.

Bulik CM, Butner JE, Tregarthen J, Thornton LM, Flatt RE, Smith T, Carroll IM, Baucom BR, Deboeck PR

The Binge Eating Genetics Initiative (BEGIN): study protocol

BMC Psychiatry 2020; 20:307.

Guintivano J, Shabalin AA, Chan RF, Rubinow DR, Sullivan PF, Meltzer-Brody S, Aberg KA, van den Oord EJ

Test-statistic inflation in methylome-wide association studies

Epigenetics 2020; 15(11):1163-1166.

Wojta K, Ayer A, Ramos EM, Nguyen PD, Karydas AM, Yokoyama JS, Kramer J, Lee SE, Boxer A, Miller BL, Coppola G

Lack of association between the CCR5-delta32 polymorphism and neurodegenerative disorders

Alzheimer disease and associated disorders 2020; 34(3):244-247.

Ali AT, Boehme L, Carbajosa G, Seitan VC, Small KS, Hodgkinson A

Nuclear genetic regulation of the human mitochondrial transcriptome

eLife 2019; 8:e41927.

Ali Aminah T, Boehme Lena, Carbajosa Guillermo, Seitan Vlad C, Small Kerrin S, Hodgkinson Alan

Nuclear genetic regulation of the human mitochondrial transcriptome.

eLife 2019; 8:.

Demontis Ditte, Walters Raymond K, Martin Joanna, Mattheisen Manuel, Als Thomas D, Agerbo Esben, Baldursson Gísli, Belliveau Rich, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Cerrato Felecia, Chambert Kimberly, Churchhouse Claire, Dumont Ashley, Eriksson Nicholas, Gandal Michael, Goldstein Jacqueline I, Grasby Katrina L, Grove Jakob, Gudmundsson Olafur O, Hansen Christine S, Hauberg Mads Engel, Hollegaard Mads V, Howrigan Daniel P, Huang Hailiang, Maller Julian B, Martin Alicia R, Martin Nicholas G, Moran Jennifer, Pallesen Jonatan, Palmer Duncan S, Pedersen Carsten Bøcker, Pedersen Marianne Giørtz, Poterba Timothy, Poulsen Jesper Buchhave, Ripke Stephan, Robinson Elise B, Satterstrom F Kyle, Stefansson Hreinn, Stevens Christine, Turley Patrick, Walters G Bragi, Won Hyejung, Wright Margaret J, ADHD Working Group of the Psychiatric Genomics Consortium (PGC) undefined, Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium undefined, 23andMe Research Team undefined, Andreassen Ole A, Asherson Philip, Burton Christie L, Boomsma Dorret I, Cormand Bru, Dalsgaard Søren, Franke Barbara, Gelernter Joel, Geschwind Daniel, Hakonarson Hakon, Haavik Jan, Kranzler Henry R, Kuntsi Jonna, Langley Kate, Lesch Klaus-Peter, Middeldorp Christel, Reif Andreas, Rohde Luis Augusto, Roussos Panos, Schachar Russell, Sklar Pamela, Sonuga-Barke Edmund J S, Sullivan Patrick F, Thapar Anita, Tung Joyce Y, Waldman Irwin D, Medland Sarah E, Stefansson Kari, Nordentoft Merete, Hougaard David M, Werge Thomas, Mors Ole, Mortensen Preben Bo, Daly Mark J, Faraone Stephen V, Børglum Anders D, Neale Benjamin M

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Nature genetics 2019; 51:63-75.

Fabbri Chiara, Kasper Siegfried, Kautzky Alexander, Bartova Lucie, Dold Markus, Zohar Joseph, Souery Daniel, Montgomery Stuart, Albani Diego, Raimondi Ilaria, Dikeos Dimitris, Rujescu Dan, Uher Rudolf, Lewis Cathryn M, Mendlewicz Julien, Serretti Alessandro

Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples

The British journal of psychiatry : the journal of mental science 2019; 214:36-41.

Fabbri Chiara, Kasper Siegfried, Kautzky Alexander, Bartova Lucie, Dold Markus, Zohar Joseph, Souery Daniel, Montgomery Stuart, Albani Diego, Raimondi Ilaria, Dikeos Dimitris, Rujescu Dan, Uher Rudolf, Lewis Cathryn M, Mendlewicz Julien, Serretti Alessandro

Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples

The British journal of psychiatry : the journal of mental science 2019; 214:36-41.

Foo Jerome C, Streit Fabian, Frank Josef, Witt Stephanie H, Treutlein Jens, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, Baune Bernhard T, Moebus Susanne, Jöckel Karl-Heinz, Forstner Andreas J, Nöthen Markus M, Rietschel Marcella, Sartorius Alexander, Kranaster Laura

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019; 180:35-45.

Grove Jakob, Ripke Stephan, Als Thomas D, Mattheisen Manuel, Walters Raymond K, Won Hyejung, Pallesen Jonatan, Agerbo Esben, Andreassen Ole A, Anney Richard, Awashti Swapnil, Belliveau Rich, Bettella Francesco, Buxbaum Joseph D, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Cerrato Felecia, Chambert Kimberly, Christensen Jane H, Churchhouse Claire, Dellenvall Karin, Demontis Ditte, De Rubeis Silvia, Devlin Bernie, Djurovic Srdjan, Dumont Ashley L, Goldstein Jacqueline I, Hansen Christine S, Hauberg Mads Engel, Hollegaard Mads V, Hope Sigrun, Howrigan Daniel P, Huang Hailiang, Hultman Christina M, Klei Lambertus, Maller Julian, Martin Joanna, Martin Alicia R, Moran Jennifer L, Nyegaard Mette, Nærland Terje, Palmer Duncan S, Palotie Aarno, Pedersen Carsten Bøcker, Pedersen Marianne Giørtz, dPoterba Timothy, Poulsen Jesper Buchhave, Pourcain Beate St, Qvist Per, Rehnström Karola, Reichenberg Abraham, Reichert Jennifer, Robinson Elise B, Roeder Kathryn, Roussos Panos, Saemundsen Evald, Sandin Sven, Satterstrom F Kyle, Davey Smith George, Stefansson Hreinn, Steinberg Stacy, Stevens Christine R, Sullivan Patrick F, Turley Patrick, Walters G Bragi, Xu Xinyi, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium undefined, BUPGEN undefined, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, 23andMe Research Team undefined, Stefansson Kari, Geschwind Daniel H, Nordentoft Merete, Hougaard David M, Werge Thomas, Mors Ole, Mortensen Preben Bo, Neale Benjamin M, Daly Mark J, Børglum Anders D

Identification of common genetic risk variants for autism spectrum disorder

Nature genetics 2019; 51:431-444.

Howard David M, Adams Mark J, Clarke Toni-Kim, Hafferty Jonathan D, Gibson Jude, Shirali Masoud, Coleman Jonathan R I, Hagenaars Saskia P, Ward Joey, Wigmore Eleanor M, Alloza Clara, Shen Xueyi, Barbu Miruna C, Xu Eileen Y, Whalley Heather C, Marioni Riccardo E, Porteous David J, Davies Gail, Deary Ian J, Hemani Gibran, Berger Klaus, Teismann Henning, Rawal Rajesh, Arolt Volker, Baune Bernhard T, Dannlowski Udo, Domschke Katharina, Tian Chao, Hinds David A, 23andMe Research Team undefined, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, Trzaskowski Maciej, Byrne Enda M, Ripke Stephan, Smith Daniel J, Sullivan Patrick F, Wray Naomi R, Breen Gerome, Lewis Cathryn M, McIntosh Andrew M

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

Nature neuroscience 2019; 22:343-352.

Li Miaoxin, Jiang Lin, Mak Timothy Shin Heng, Kwan Johnny Sheung Him, Xue Chao, Chen Peikai, Leung Henry Chi-Ming, Cui Liqian, Li Tao, Sham Pak Chung

A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia

Bioinformatics (Oxford, England) 2019; 35:628-635.

Pearl JR, Colantuoni C, Bergey DE, Funk CC, Basu B, Casella AM, Oshone RT, Shannon P, Hood L, Price ND, Ament SA

Genome-scale transcriptional regulatory network models of psychiatric and neurodegenerative disorders.

Cell Systems 2019; In press:.

Polimanti Renato, Peterson Roseann E, Ong Jue-Sheng, MacGregor Stuart, Edwards Alexis C, Clarke Toni-Kim, Frank Josef, Gerring Zachary, Gillespie Nathan A, Lind Penelope A, Maes Hermine H, Martin Nicholas G, Mbarek Hamdi, Medland Sarah E, Streit Fabian, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, Agrawal Arpana, Edenberg Howard J, Kendler Kenneth S, Lewis Cathryn M, Sullivan Patrick F, Wray Naomi R, Gelernter Joel, Derks Eske M

Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium

Psychological medicine 2019; 1-9.

Schork Andrew J, Won Hyejung, Appadurai Vivek, Nudel Ron, Gandal Mike, Delaneau Olivier, Revsbech Christiansen Malene, Hougaard David M, Bækved-Hansen Marie, Bybjerg-Grauholm Jonas, Giørtz Pedersen Marianne, Agerbo Esben, Bøcker Pedersen Carsten, Neale Benjamin M, Daly Mark J, Wray Naomi R, Nordentoft Merete, Mors Ole, Børglum Anders D, Bo Mortensen Preben, Buil Alfonso, Thompson Wesley K, Geschwind Daniel H, Werge Thomas

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

Nature neuroscience 2019; 22:353-361.

Trzaskowski Maciej, Mehta Divya, Peyrot Wouter J, Hawkes David, Davies Daniel, Howard David M, Kemper Kathryn E, Sidorenko Julia, Maier Robert, Ripke Stephan, Mattheisen Manuel, Baune Bernhard T, Grabe Hans J, Heath Andrew C, Jones Lisa, Jones Ian, Madden Pamela A F, McIntosh Andrew M, Breen Gerome, Lewis Cathryn M, Børglum Anders D, Sullivan Patrick F, Martin Nicholas G, Kendler Kenneth S, Levinson Douglas F, Wray Naomi R, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined

Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019; 10.1002/ajmg.b.32713.

Wheeler HE, Ploch S, Barbeira AN, Bonazzola R, Andaleon A, Fotuhi Siahpirani A, Saha A, Battle A, Roy S, Im HK

Imputed gene associations identify replicable trans-acting genes enriched in transcription pathways and complex traits

Genetic Epidemiology 2019; 43(6):596-608.

Amare Azmeraw T., Schubert Klaus Oliver, Tekola-Ayele Fasil, Hsu Yi-Hsiang, Sangkuhl Katrin, Jenkins Gregory, Whaley Ryan M., Barman Poulami, Batzler Anthony, Altman Russ B., Arolt Volker, Brockmöller Jürgen, Chen Chia-Hui, Domschke Katharina, Hall-Flavin Daniel K., Hong Chen-Jee, Illi Ari, Ji Yuan, Kampman Olli, Kinoshita Toshihiko, Leinonen Esa, Liou Ying-Jay, Mushiroda Taisei, Nonen Shinpei, Skime Michelle K., Wang Liewei, Kato Masaki, Liu Yu-Li, Praphanphoj Verayuth, Stingl Julia C., Bobo William V., Tsai Shih-Jen, Kubo Michiaki, Klein Teri E., Weinshilboum Richard M., Biernacka Joanna M., Baune Bernhard T.

Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder

Frontiers in Psychiatry 2018; 9:65.

Barbeira AN, Dickinson SP, Bonazzola R, Zheng J, Wheeler HE, Torres JM, Torstenson ES, Shah KP, Garcia T, Edwards TL, Stahl EA, Huckins LM, Nicolae DL, Cox NJ, Im HK

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Nature Communications 2018; 9:1.

Bauer Anna E., Maegbaek Merete L., Liu Xiaoqin, Wray Naomi R., Sullivan Patrick F., Miller William C., Meltzer-Brody Samantha, Munk-Olsen Trine

Familiality of psychiatric disorders and risk of postpartum psychiatric episodes: A population-based cohort study

The American journal of psychiatry 2018; 175:783-791.

Blokland Gabriëlla A M, Del Re Elisabetta C, Mesholam-Gately Raquelle I, Jovicich Jorge, Trampush Joey W, Keshavan Matcheri S, DeLisi Lynn E, Walters James T R, Turner Jessica A, Malhotra Anil K, Lencz Todd, Shenton Martha E, Voineskos Aristotle N, Rujescu Dan, Giegling Ina, Kahn René S, Roffman Joshua L, Holt Daphne J, Ehrlich Stefan, Kikinis Zora, Dazzan Paola, Murray Robin M, Di Forti Marta, Lee Jimmy, Sim Kang, Lam Max, Wolthusen Rick P F, de Zwarte Sonja M C, Walton Esther, Cosgrove Donna, Kelly Sinead, Maleki Nasim, Osiecki Lisa, Picchioni Marco M, Bramon Elvira, Russo Manuela, David Anthony S, Mondelli Valeria, Reinders Antje A T S, Falcone M Aurora, Hartmann Annette M, Konte Bettina, Morris Derek W, Gill Michael, Corvin Aiden P, Cahn Wiepke, Ho New Fei, Liu Jian Jun, Keefe Richard S E, Gollub Randy L, Manoach Dara S, Calhoun Vince D, Schulz S Charles, Sponheim Scott R, Goff Donald C, Buka Stephen L, Cherkerzian Sara, Thermenos Heidi W, Kubicki Marek, Nestor Paul G, Dickie Erin W, Vassos Evangelos, Ciufolini Simone, Reis Marques Tiago, Crossley Nicolas A, Purcell Shaun M, Smoller Jordan W, van Haren Neeltje E M, Toulopoulou Timothea, Donohoe Gary, Goldstein Jill M, Seidman Larry J, McCarley Robert W, Petryshen Tracey L

The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project

Schizophrenia research 2018; 195:306-317.

Byrne Enda M, Ferreira Manuel A R, Xue Angli, Lindström Sara, Jiang Xia, Yang Jian, Easton Douglas F, Wray Naomi R, Chenevix-Trench Georgia

Is Schizophrenia a Risk Factor for Breast Cancer?-Evidence From Genetic Data

Schizophrenia bulletin 2018; Epub:10.1093/schbul/sby162.

Cheng H, Xuan H, Green CD, Han Y, Sun N, Shen H, McDermott J, Bennett DA, Lan F, Han JJ

Repression of human and mouse brain inflammaging transcriptome by broad gene-body histone hyperacetylation

Proc Natl Acad Sci U S A 2018

Cheng H, Xuan H, Green CD, Han Y, Sun N, Shen H, McDermott J, Bennett DA, Lan F, Han JJ

Repression of human and mouse brain inflammaging transcriptome by broad gene-body histone hyperacetylation

Proc Natl Acad Sci U S A 2018

Drago A, Calabro M, Crisafulli C, Rasmussen SK

Genetic Insights from a Molecular Pathway Analysis on Two Independent Samples of Autistic Patients

Journal of Molecular and Genetic Medicine 2018; 12:1.

Eyles Darryl W, Trzaskowski Maciej, Vinkhuyzen Anna A E, Mattheisen Manuel, Meier Sandra, Gooch Helen, Anggono Victor, Cui Xiaoying, Tan Men Chee, Burne Thomas H J, Jang Se Eun, Kvaskoff David, Hougaard David M, Nørgaard-Pedersen Bent, Cohen Arieh, Agerbo Esben, Pedersen Carsten B, Børglum Anders D, Mors Ole, Sah Pankaj, Wray Naomi R, Mortensen Preben B, McGrath John J

The association between neonatal vitamin D status and risk of schizophrenia

Scientific reports 2018; 8:17692.

Fabbri Chiara, Kasper Siegfried, Kautzky Alexander, Bartova Lucie, Dold Markus, Zohar Joseph, Souery Daniel, Montgomery Stuart, Albani Diego, Raimondi Ilaria, Dikeos Dimitris, Rujescu Dan, Uher Rudolf, Lewis Cathryn M, Mendlewicz Julien, Serretti Alessandro

Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples

The British journal of psychiatry 2018

Giacopuzzi Edoardo, Gennarelli Massimo, Sacco Chiara, Filippini Alice, Mingardi Jessica, Magri Chiara, Barbon Alessandro

Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variables.

BMC genomics 2018; 19(1):963.

Giambartolomei C, Zhenli Liu J, Zhang W, Hauberg M, Shi H, Boocock J, Pickrell J, Jaffe AE; CommonMind Consortium, Pasaniuc B, Roussos P

A Bayesian Framework for Multiple Trait Colo-calization from Summary Association Statistics.

Bioinformatics 2018; In Press:.

Glassberg Emily C, Gao Ziyue, Harpak Arbel, Lan Xun, Pritchard Jonathan K

Evidence for Weak Selective Constraint on Human Gene Expression

Genetics 2018; genetics.301833.2018.

Gonçalves Vanessa F, Cappi Carolina, Hagen Christian M, Sequeira Adolfo, Vawter Marquis P, Derkach Andriy, Zai Clement C, Hedley Paula L, Bybjerg-Grauholm Jonas, Pouget Jennie G, Cuperfain Ari B, Sullivan Patrick F, Christiansen Michael, Kennedy James L, Sun Lei

A Comprehensive Analysis of Nuclear-Encoded Mitochondrial Genes in Schizophrenia

Biological psychiatry 2018; 83:780-789.

Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X.

A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

American Journal of Human Genetics 2018; 102:6.

Marceau R, Lu W, Yilmaz Z, Bulik C, Crowley J, Mattheisen M, Sullivan P, PGC-ED, PGC-OCD, The Swedish Schizophrenia Study, Szatkiewicz J, Tzeng JY

Variance Component Test for Cross-Disorder Pathway Analysis

Abstract of World Congress of Psychiatric Genetics 2018 2018

Martin Joanna, Walters Raymond K., Demontis Ditte, Mattheisen Manuel, Lee S. Hong, Robinson Elise, Brikell Isabell, Ghirardi Laura, Larsson Henrik, Lichtenstein Paul, Eriksson Nicholas, 23andMe Research TeamAgeeMichelleAlipanahiBabakAutonAdamBellRobert K.BrycKatarzynaElsonSarah L.FontanillasPierreFurlotteNicholas A.HindsDavid A.HromatkaBethann S.HuberKaren E.KleinmanAaronLittermanNadia K.McIntyreMatthew H.MountainJoanna L.NorthoverCarrie A.M.PittsSteven J.SathirapongsasutiJ. FahSazonovaOlga V.SheltonJanie F.ShringarpureSuyashTianChaoTungJoyce Y.VacicVladimirWilsonCatherine H. undefined, Agee Michelle, Alipanahi Babak, Auton Adam, Bell Robert K., Bryc Katarzyna, Elson Sarah L., Fontanillas Pierre, Furlotte Nicholas A., Hinds David A., Hromatka Bethann S., Huber Karen E., Kleinman Aaron, Litterman Nadia K., McIntyre Matthew H., Mountain Joanna L., Northover Carrie A.M., Pitts Steven J., Sathirapongsasuti J. Fah, Sazonova Olga V., Shelton Janie F., Shringarpure Suyash, Tian Chao, Tung Joyce Y., Vacic Vladimir, W

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

Biological Psychiatry 2018; 83:1044-1053.

Middeldorp Christel M., Wray Naomi R.

The value of polygenic analyses in psychiatry

World Psychiatry 2018; 17:26-28.

Minică Camelia C, Verweij Karin J H, van der Most Peter J, Mbarek Hamdi, Bernard Manon, van Eijk Kristel R, Lind Penelope A, Liu Meng Zhen, Maciejewski Dominique F, Palviainen Teemu, Sánchez-Mora Cristina, Sherva Richard, Taylor Michelle, Walters Raymond K, Abdellaoui Abdel, Bigdeli Timothy B, Branje Susan J T, Brown Sandra A, Casas Miguel, Corley Robin P, Davey-Smith George, Davies Gareth E, Ehli Erik A, Farrer Lindsay, Fedko Iryna O, Garcia-Martínez Iris, Gordon Scott D, Hartman Catharina A, Heath Andrew C, Hickie Ian B, Hickman Matthew, Hopfer Christian J, Hottenga Jouke Jan, Kahn René S, Kaprio Jaakko, Korhonen Tellervo, Kranzler Henry R, Krauter Ken, van Lier Pol A C, Madden Pamela A F, Medland Sarah E, Neale Michael C, Meeus Wim H J, Montgomery Grant W, Nolte Ilja M, Oldehinkel Albertine J, Pausova Zdenka, Ramos-Quiroga Josep A, Richarte Vanesa, Rose Richard J, Shin Jean, Stallings Michael C, Wall Tamara L, Ware Jennifer J, Wright Margaret J, Zhao Hongyu, Koot Hans M, Paus Tomas, Hewitt John K, Ribasés Marta, Loukola Anu, Boks Marco P, Snieder Harold, Munafò Marcus R, Gelernter Joel, Boomsma Dorret I, Martin Nicholas G, Gillespie Nathan A, Vink Jacqueline M, Derks Eske M

Genome-wide association meta-analysis of age at first cannabis use.

Addiction (Abingdon, England) 2018; 113(11):2073-2086.

Ni G, Gratten J, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Scientific Reports 2018; 1:10.

Niarchou M, Chawner SJRA, Fiksinski A, Vorstman JAS, Maeder J, Schneider M, Eliez S, Armando M, Pontillo M, Vicari S, McDonald-McGinn DM, Emanuel BS, Zackai EH, Bearden CE, Shashi V, Hooper SR, Owen MJ, Gur RE, Wray NR, van den Bree MBM, Thapar A; International 22q11.2 Deletion Syndrome Brain and Behavior Consortium.

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome.

Schizophrenia Research 2018; Online only:Online only.

Reinbold Céline S., Forstner Andreas J., Hecker Julian, Fullerton Janice M., Hoffmann Per, Hou Liping, Heilbronner Urs, Degenhardt Franziska, Adli Mazda, Akiyama Kazufumi, Akula Nirmala, Ardau Raffaella, Arias Bárbara, Backlund Lena, Benabarre Antonio, Bengesser Susanne, Bhattacharjee Abesh K., Biernacka Joanna M., Birner Armin, Marie-Claire Cynthia, Cervantes Pablo, Chen Guo-Bo, Chen Hsi-Chung, Chillotti Caterina, Clark Scott R., Colom Francesc, Cousins David A., Cruceanu Cristiana, Czerski Piotr M., Dayer Alexandre, Étain Bruno, Falkai Peter, Frisén Louise, Gard Sébastien, Garnham Julie S., Goes Fernando S., Grof Paul, Gruber Oliver, Hashimoto Ryota, Hauser Joanna, Herms Stefan, Jamain Stéphane, Jiménez Esther, Kahn Jean-Pierre, Kassem Layla, Kittel-Schneider Sarah, Kliwicki Sebastian, König Barbara, Kusumi Ichiro, Lackner Nina, Laje Gonzalo, Landén Mikael, Lavebratt Catharina, Leboyer Marion, Leckband Susan G., López Jaramillo Carlos A., MacQueen Glenda, Manchia Mirko, Martinsson Lina, Mattheisen Manuel, McCarthy Michael J., McElroy Susan L., Mitjans Marina, Mondimore Francis M., Monteleone Palmiero, Nievergelt Caroline M., Ösby Urban, Ozaki Norio, Perlis Roy H., Pfennig Andrea, Reich-Erkelenz Daniela, Rouleau Guy A., Schofield Peter R., Schubert K. Oliver, Schweizer Barbara W., Seemüller Florian, Severino Giovanni, Shekhtman Tatyana, Shilling Paul D., Shimoda Kazutaka, Simhandl Christian, Slaney Claire M., Smoller Jordan W., Squassina Alessio, Stamm Thomas J., Stopkova Pavla, Tighe Sarah K., Tortorella Alfonso, Turecki Gustavo, Volkert Julia, Witt Stephanie H., Wright Adam J., Young L. Trevor, Zandi Peter P., Potash James B., DePaulo J. Raymond, Bauer Michael, Reininghaus Eva, Novák Tomáš, Aubry Jean-Michel, Maj Mario, Baune Bernhard T., Mitchell Philip B., Vieta Eduard, Frye Mark A., Rybakowski Janusz K., Kuo Po-Hsiu, Kato Tadafumi, Grigoroiu-Serbanescu Maria, Reif Andreas, Del Zompo Maria, Bellivier Frank, Schalling Martin, Wray Naomi R., Kelsoe John R., Alda Martin, McMahon Francis J., Schulze Thomas G., Rietschel Marcella, Nöthen Markus M., Cichon Sven

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder

Frontiers in Psychiatry 2018; 9:207.

Roessler Reinhard, Goldmann Johanna, Shivalila Chikdu, Jaenisch Rudolf

JIP2 haploinsufficiency contributes to neurodevelopmental abnormalities in human pluripotent stem cell-derived neural progenitors and cortical neurons.

Life science alliance 2018; 1(4):e201800094.

Story Jovanova O, Nedeljkovic I, Derek S, Walker RM, Liu C, Luciano M, Bressler J, Brody J, Drake AJ, Evans KL, Gondalia R, Kunze S, Kuhnel B, Lahti J, Lemaitre RN, Marioni RE, Swenson B, Himali JJ, Wu H, Li Y, McRae AF, Russ TC, Stewart J, Wang Z, Zhang G, Ladwig KH, Uitterlinden AG, Guo X, Peters A, Räikkönen K, Starr JM, Waldenberger M, Wray NR, Whitsel EA, Sotoodehnia N, Seshadri S, Porteous DJ, van Meurs J, Mosley TH, McIntosh AM, Mendelson MM, Levy D, Hou L, Eriksson JG, Fornage M, Deary IJ, Baccarelli A, Tiemeier H, Amin N.

DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide Studies.

JAMA Psychiatry 2018; 75:9.

The childhood trauma working-group of PGC-MDD undefined, Van der Auwera S, Peyrot WJ, Milaneschi Y, Hertel J, Baune BT, Breen G, Byrne EM, Dunn EC, Fisher HL, Homuth G, Levinson DF, Lewis CM, Mills N, Mullins N, Nauck M, Pistis G, Preisig M, Rietschel M, Ripke S, Sullivan PF, Teumer A, Völzke H, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, Boomsma DI, Wray NR, Penninx BWJH, Grabe HJ

GENOME-WIDE GENE-ENVIRONMENT INTERACTION IN DEPRESSION: A SYSTEMATIC EVALUATION OF CANDIDATE GENES

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018; 177:40-49.

Wray Naomi R, Ripke Stephan, Mattheisen Manuel, Trzaskowski Maciej, Byrne Enda M, Abdellaoui Abdel, Adams Mark J, Agerbo Esben, Air Tracy M, Andlauer Till F M, Bacanu Silviu-Alin, Bækvad-Hansen Marie, Beekman Aartjan T F, Bigdeli Tim B, Binder Elisabeth B, Blackwood Douglas H R, Bryois Julien, Buttenschøn Henriette N, Bybjerg-Grauholm Jonas, Cai Na, Castelao Enrique, Christensen Jane Hvarregaard, Clarke Toni-Kim, Coleman Jonathan R I, Colodro-Conde Lucía, Couvy-Duchesne Baptiste, Craddock Nick, Crawford Gregory E, Crowley Cheynna A, Dashti Hassan S, Davies Gail, Deary Ian J, Degenhardt Franziska, Derks Eske M, Direk Nese, Dolan Conor V, Dunn Erin C, Eley Thalia C, Eriksson Nicholas, Escott-Price Valentina, Kiadeh Farnush Farhadi Hassan, Finucane Hilary K, Forstner Andreas J, Frank Josef, Gaspar Héléna A, Gill Michael, Giusti-Rodríguez Paola, Goes Fernando S, Gordon Scott D, Grove Jakob, Hall Lynsey S, Hannon Eilis, Hansen Christine Søholm, Hansen Thomas F, Herms Stefan, Hickie Ian B, Hoffmann Per, Homuth Georg, Horn Carsten, Hottenga Jouke-Jan, Hougaard David M, Hu Ming, Hyde Craig L, Ising Marcus, Jansen Rick, Jin Fulai, Jorgenson Eric, Knowles James A, Kohane Isaac S, Kraft Julia, Kretzschmar Warren W., Krogh Jesper, Kutalik Zoltán, Lane Jacqueline M, Li Yihan, Li Yun, Lind Penelope A, Liu Xiaoxiao, Lu Leina, MacIntyre Donald J, MacKinnon Dean F, Maier Robert M, Maier Wolfgang, Marchini Jonathan, Mbarek Hamdi, McGrath Patrick, McGuffin Peter, Medland Sarah E, Mehta Divya, Middeldorp Christel M, Mihailov Evelin, Milaneschi Yuri, Milani Lili, Mill Jonathan, Mondimore Francis M, Montgomery Grant W, Mostafavi Sara, Mullins Niamh, Nauck Matthias, Ng Bernard, Nivard Michel G, Nyholt Dale R, O’Reilly Paul F, Oskarsson Hogni, Owen Michael J, Painter Jodie N, Pedersen Carsten Bøcker, Pedersen Marianne Giørtz, Peterson Roseann E., Pettersson Erik, Peyrot Wouter J, Pistis Giorgio, Posthuma Danielle, Purcell Shaun M, Quiroz Jorge A, Qvist Per, Rice John P, Riley Brien P., Rivera Margarita, Mirza Saira Saeed, Saxena Richa, Schoevers Robert, Schulte Eva C, Shen Ling, Shi Jianxin, Shyn Stanley I, Sigurdsson Engilbert, Sinnamon Grant C B, Smit Johannes H, Smith Daniel J, Stefansson Hreinn, Steinberg Stacy, Stockmeier Craig A, Streit Fabian, Strohmaier Jana, Tansey Katherine E, Teismann Henning, Teumer Alexander, Thompson Wesley, Thomson Pippa A, Thorgeirsson Thorgeir E, Tian Chao, Traylor Matthew, Treutlein Jens, Trubetskoy Vassily, Uitterlinden André G, Umbricht Daniel, Van der Auwera Sandra, van Hemert Albert M, Viktorin Alexander, Visscher Peter M, Wang Yunpeng, Webb Bradley T., Weinsheimer Shantel Marie, Wellmann Jürgen, Willemsen Gonneke, Witt Stephanie H, Wu Yang, Xi Hualin S, Yang Jian, Zhang Futao, eQTLGen Consortium undefined, 23andMe Research Team undefined, Arolt Volker, Baune Bernhard T, Berger Klaus, Boomsma Dorret I, Cichon Sven, Dannlowski Udo, de Geus EJC, DePaulo J Raymond, Domenici Enrico, Domschke Katharina, Esko Tõnu, Grabe Hans J, Hamilton Steven P, Hayward Caroline, Heath Andrew C, Hinds David A, Kendler Kenneth S, Kloiber Stefan, Lewis Glyn, Li Qingqin S, Lucae Susanne, Madden Pamela AF, Magnusson Patrik K, Martin Nicholas G, McIntosh Andrew M, Metspalu Andres, Mors Ole, Mortensen Preben Bo, Müller-Myhsok Bertram, Nordentoft Merete, Nöthen Markus M, O’Donovan Michael C, Paciga Sara A, Pedersen Nancy L, Penninx Brenda WJH, Perlis Roy H, Porteous David J, Potash James B, Preisig Martin, Rietschel Marcella, Schaefer Catherine, Schulze Thomas G, Smoller Jordan W, Stefansson Kari, Tiemeier Henning, Uher Rudolf, Völzke Henry, Weissman Myrna M, Werge Thomas, Winslow Ashley R, Lewis Cathryn M, Levinson Douglas F, Breen Gerome, Børglum Anders D, Sullivan Patrick F

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Nature genetics 2018; 50:668-681.

Wu Y, Zeng J, Zhang F, Zhu Z, Qi T, Zheng Z, Lloyd-Jones LR, Marioni RE, Martin NG, Montgomery GW, Deary IJ, Wray NR, Visscher PM, McRae AF & Yang J

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

Nature Communications 2018; 9:918.

Zhang S, Moy W, Zhang H, Leites C, McGowan H, Shi J, Sanders AR, Pang Z, Gejman PV, Duan J.

Open Chromatin Dynamics Reveals Stage-specific Transcriptional Networks in hiPSC-based neurodevelopmental model

Stem Cell Res. 2018; 29:.

DeMichele-Sweet MAA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, Lopez OL, Sibille EL, Kamboh MI, Devlin B, Sweet RA.

Genetic risk for schizophrenia and psychosis in Alzheimer disease.

Mol Psychiatry 2017

Fabbri C, Crisafulli C, Calati R, Albani D, Forloni G, Calabrò M, Martines R,4, Kasper S, Zohar J, Juven-Wetzler A, Souery D, Montgomery S, Mendlewicz J, Serretti A

Neuroplasticity and second messenger pathways in antidepressant efficacy: pharmacogenetic results from a prospective trial investigating treatment resistance.

Eur Arch Psychiatry Clin Neurosci 2017; Epub ahead of print:.

Fabbri C, Boriani G, Diemberger I, Filippi MG, Ravegnini G, Hrelia P, Minarini A, Albani D, Forloni G, Angelini S, Serretti A

Electrocardiogram Alterations Associated With Psychotropic Drug Use and CACNA1C Gene Variants in Three Independent Samples

Basic Clin Pharmacol Toxicol 2017; 120:5.

Fabbri C, Corponi F, Albani D, Raimondi I, Forloni G, Schruers K, Kasper S, Kautzky A, Zohar J, Souery D, Montgomery S, Cristalli CP, Mantovani V, Mendlewicz J, Serretti A

Pleiotropic genes in psychiatry: Calcium channels and the stress-related FKBP5 gene in antidepressant resistance

Prog Neuropsychopharmacol Biol Psychiatry 2017; 81:2.

Forrest Marc P., Zhang Hanwen, Moy Winton, McGowan Heather, Leites Catherine, Dionisio Leonardo E., Xu Zihui, Shi Jianxin, Sanders Alan R., Greenleaf William J., Cowan Chad A., Pang Zhiping P., Gejman Pablo V., Penzes Peter, Duan Jubao

Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci

Cell stem cell 2017; 21:305-318.e8.

Hauberg ME, Zhang W, Giambartolomei C, Franzén O, Morris DL, Vyse TJ, Ruusalepp A; CommonMind Consortium, Sklar P, Schadt EE, Björkegren JLM, Roussos P.

Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression.

Am J Hum Genet 2017; 100:6.

Lee BS, McIntyre RS, Gentle JE, Park NS, Chiriboga DA, Lee Y, Singh S, McPherson MA

A computational algorithm for personalized medicine in schizophrenia

Schizophrenia Research 2017

Lim K, Lam M, Liu JJ, Lee J.

Genome-wide association of tardive dyskinesia

Abstract accepted by the World Congress of Psychiatric Genetic 2017 2017

Palmer Rohan H. C., Beevers Christopher G., McGeary John E., Brick Leslie A, Knopik Valerie S

A Preliminary Study of Genetic Variation in the Dopaminergic and Serotonergic Systems and Genome-wide Additive Genetic Effects on Depression Severity and Treatment Response

Clinical psychological science : a journal of the Association for Psychological Science 2017; 5:158-165.

Peyrot Wouter J, Van der Auwera Sandra, Milaneschi Yuri, Dolan Conor V, Madden Pamela AF, Sullivan Patrick F, Strohmaier Jana, Ripke Stephan, Rietschel Marcella, Nivard Michel G, Mullins Niamh, Montgomery Grant W, Henders Anjali K, Heat Andrew C, Fisher Helen L, Dunn Erin C, Byrne Enda M, Air Tracy A, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium undefined, Baune Bernhard T, Breen Gerome, Levinson Douglas F, Lewis Cathryn M, Martin Nick G, Nelson Elliot N, Boomsma Dorret I, Grabe Hans J, Wray Naomi R, Penninx Brenda WJH

Does childhood trauma moderate polygenic risk for depression? A meta-analysis of 5,765 subjects from the Psychiatric Genomics Consortium

Biological psychiatry 2017; S0006-3223(17)31993-5.

Qi Y, Zheng Y, Li Z, Xiong L

Progress in Genetic Studies of Tourette's Syndrome

Brain Sciences 2017; 7(10):134.

Yengo Loic, Zhu Zhihong, Wray Naomi R., Weir Bruce S., Yang Jian, Robinson Matthew R., Visscher Peter M.

Detection and quantification of inbreeding depression for complex traits from SNP data

Proceedings of the National Academy of Sciences of the United States of America 2017; 114:8602-8607.

Zhu L, Lei J, Devlin B, Roeder K.

TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES.

Annals of Applied Statistics 2017; 11:3.

Cocchi E, Fabbri C, Han C, Lee SJ, Patkar AA, Masand PS, Pae CU, Serretti A

Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway

BMC Psychiatry 2016; 16:.

Ellis SE, Panitch R, West AB, Arking DE

Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia

Translational Psychiatry 2016; 6(5):e817-.

Fabbri C, Boriani G, Diemberger I, Filippi MG, Ravegnini G, Hrelia P, Minarini A, Albani D, Forloni G, Angelini S, Serretti A

Electrocardiogram Alterations Associated With Psychotropic Drug Use and CACNA1C Gene Variants in Three Independent Samples.

Basic Clin Pharmacol Toxicol. 2016; Epub ahead of print:.

Kao Chung-Feng, Chen Hui-Wen, Chen Hsi-Chung, Yang Jenn-Hwai, Huang Ming-Chyi, Chiu Yi-Hang, Lin Shih-Ku, Lee Ya-Chin, Liu Chih-Min, Chuang Li-Chung, Chen Chien-Hsiun, Wu Jer-Yuarn, Lu Ru-Band, Kuo Po-Hsiu

Identification of Susceptible Loci and Enriched Pathways for Bipolar II Disorder Using Genome-Wide Association Studies

International Journal of Neuropsychopharmacology 2016; 19:pyw064.

Li M, Jaffe AE, Straub RE, Tao R, Shin JH, Wang Y, Chen Q, Li C, Jia Y, Ohi K, Maher BJ, Brandon NJ, Cross A, Chenoweth JG, Hoeppner DJ, Wei H, Hyde TM, McKay R, Kleinman JE, Weinberger DR

A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.

Nature Medicine 2016; 22:.

Pandey JP, Namboodiri AM, Elston RC

Immunoglobulin G genotypes and the risk of schizophrenia.

Human Genetics 2016; 135:10.

Pearson Rahel, Palmer Rohan H. C., Brick Leslie A., McGeary John E., Knopik Valerie S., Beevers Christopher G.

Additive Genetic Contribution to Symptom Dimensions in Major Depressive Disorder

Journal of abnormal psychology 2016; 125:495-501.

Sakurai K, Kurtz A, Stacey G, Sheldon M, Fujibuchi W

First Proposal of Minimum Information About a Cellular Assay for Regenerative Medicine

Stem Cells Translational Medicine 2016; sctm. 2015-0393.

Sharon Eilon, Sibener Leah V., Battle Alexis, Fraser Hunter B., Garcia K. Christopher, Pritchard Jonathan K.

Genetic variation in MHC proteins is associated with T cell receptor expression biases

Nature genetics 2016; 48:995-1002.

Vervier Kévin, Michaelson Jacob J.

SLINGER: large-scale learning for predicting gene expression

Scientific Reports 2016; 6:39360.

Wheeler HE, Shah KP, Brenner J, Garcia T, Aquino-Michaels K; GTEx Consortium, Cox NJ, Nicolae DL, Im HK

Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.

PLoS Genet. 2016; 12:11.

Drago A, Monti B, De Ronchi D, Serretti A

CRY1 Variations Impacts on the Depressive Relapse Rate in a Sample of Bipolar Patients

Psychiatry Investig 2015; 12:118-24.

Fabbri C, Crisafulli C, Gurwitz D, Stingl J, Calati R, Albani D, Forloni G, Calabrò M, Martines R, Kasper S, Zohar J, Juven-Wetzler A, Souery D, Montgomery S, Mendlewicz J, Girolamo GD, Serretti A

Neuronal cell adhesion genes and antidepressant response in three independent samples

Pharmacogenomics J. 2015; 15:538-48.

Gamazon ER, Wheeler HE, Shah KP, Mozaffari SV, Aquino-Michaels K, Carroll RJ, Eyler AE, Denny JC; GTEx Consortium, Nicolae DL, Cox NJ, Im HK.

A gene-based association method for mapping traits using reference transcriptome data.

Nat Genet. 2015; 47:9.

Lehner T, Senthil G, Addington AM

Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics

Biological psychiatry 2015; 77(1):6-14.

Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D

Loss of [dgr]-catenin function in severe autism

Nature 2015; 520(7545):51-56.

Antypa N, Drago A, Serretti A

Genomewide interaction and enrichment analysis on antidepressant response

Psychol Med 2014; 44:753-65.

Battle A, Mostafavi S, Zhu X, Potash JB, Weissman MM, McCormick C, Haudenschild CD, Beckman KB, Shi J, Mei R

Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals

Genome research 2014; 24(1):14-24.

Doyle GA, Chou AD, Saung WT, Lai AT, Lohoff FW, Berrettini WH

Identification of CHRNA5 rare variants in African-American heavy smokers

Psychiatric genetics 2014; 24(3):102-109.

Evangelou M, Smyth DJ, Fortune MD, Burren OS, Walker NM, Guo H, Onengut-Gumuscu S, Chen WM, Concannon P, Rich SS, Todd JA, Wallace C

A Method for Gene-Based Pathway Analysis Using Genomewide Association Study Summary Statistics Reveals Nine New Type 1 Diabetes Associations

Genetic Epidemiology 2014; 38(8):661-670.

Lohoff FW, Hodge R, Narasimhan S, Nall A, Ferraro TN, Mickey BJ, Heitzeg MM, Langenecker SA, Zubieta JK, Bogdan R, Nikolova YS, Drabant E, Hariri AR, Bevilacqua L, Goldman D, Doyle GA

Functional genetic variants in the vesicular monoamine transporter 1 (VMAT1) modulate emotion processing

Molecular psychiatry 2014; 19(1):129-139.

Berndt Sonja I., Gustafsson Stefan, Mägi Reedik, Ganna Andrea, Wheeler Eleanor, Feitosa Mary F., Justice Anne E., Monda Keri L., Croteau-Chonka Damien C., Day Felix R., Esko Tõnu, Fall Tove, Ferreira Teresa, Gentilini Davide, Jackson Anne U., Luan Jian’an, Randall Joshua C., Vedantam Sailaja, Willer Cristen J., Winkler Thomas W., Wood Andrew R., Workalemahu Tsegaselassie, Hu Yi-Juan, Lee Sang Hong, Liang Liming, Lin Dan-Yu, Min Josine L., Neale Benjamin M., Thorleifsson Gudmar, Yang Jian, Albrecht Eva, Amin Najaf, Bragg-Gresham Jennifer L., Cadby Gemma, den Heijer Martin, Eklund Niina, Fischer Krista, Goel Anuj, Hottenga Jouke-Jan, Huffman Jennifer E., Jarick Ivonne, Johansson Åsa, Johnson Toby, Kanoni Stavroula, Kleber Marcus E., König Inke R., Kristiansson Kati, Kutalik Zoltán, Lamina Claudia, Lecoeur Cecile, Li Guo, Mangino Massimo, McArdle Wendy L., Medina-Gomez Carolina, Müller-Nurasyid Martina, Ngwa Julius S., Nolte Ilja M., Paternoster Lavinia, Pechlivanis Sonali, Perola Markus, Peters Marjolein J., Preuss Michael, Rose Lynda M., Shi Jianxin, Shungin Dmitry, Smith Albert Vernon, Strawbridge Rona J., Surakka Ida, Teumer Alexander, Trip Mieke D., Tyrer Jonathan, Van Vliet-Ostaptchouk Jana V., Vandenput Liesbeth, Waite Lindsay L., Zhao Jing Hua, Absher Devin, Asselbergs Folkert W., Atalay Mustafa, Attwood Antony P., Balmforth Anthony J., Basart Hanneke, Beilby John, Bonnycastle Lori L., Brambilla Paolo, Bruinenberg Marcel, Campbell Harry, Chasman Daniel I., Chines Peter S., Collins Francis S., Connell John M., Cookson William, de Faire Ulf, de Vegt Femmie, Dei Mariano, Dimitriou Maria, Edkins Sarah, Estrada Karol, Evans David M., Farrall Martin, Ferrario Marco M., Ferrières Jean, Franke Lude, Frau Francesca, Gejman Pablo V., Grallert Harald, Grönberg Henrik, Gudnason Vilmundur, Hall Alistair S., Hall Per, Hartikainen Anna-Liisa, Hayward Caroline, Heard-Costa Nancy L., Heath Andrew C., Hebebrand Johannes, Homuth Georg, Hu Frank B., Hunt Sarah E., Hyppönen Elina, Iribarren Carlos, Jacobs Kevin B., Jansson John-Olov, Jula Antti, Kähönen Mika, Kathiresan Sekar, Kee Frank, Khaw Kay-Tee, Kivimaki Mika, Koenig Wolfgang, Kraja Aldi T., Kumari Meena, Kuulasmaa Kari, Kuusisto Johanna, Laitinen Jaana H., Lakka Timo A., Langenberg Claudia, Launer Lenore J., Lind Lars, Lindström Jaana, Liu Jianjun, Liuzzi Antonio, Lokki Marja-Liisa, Lorentzon Mattias, Madden Pamela A., Magnusson Patrik K., Manunta Paolo, Marek Diana, März Winfried, Mateo Leach Irene, McKnight Barbara, Medland Sarah E., Mihailov Evelin, Milani Lili, Montgomery Grant W., Mooser Vincent, Mühleisen Thomas W., Munroe Patricia B., Musk Arthur W., Narisu Narisu, Navis Gerjan, Nicholson George, Nohr Ellen A., Ong Ken K., Oostra Ben A., Palmer Colin N.A., Palotie Aarno, Peden John F., Pedersen Nancy, Peters Annette, Polasek Ozren, Pouta Anneli, Pramstaller Peter P., Prokopenko Inga, Pütter Carolin, Radhakrishnan Aparna, Raitakari Olli, Rendon Augusto, Rivadeneira Fernando, Rudan Igor, Saaristo Timo E., Sambrook Jennifer G., Sanders Alan R., Sanna Serena, Saramies Jouko, Schipf Sabine, Schreiber Stefan, Schunkert Heribert, Shin So-Youn, Signorini Stefano, Sinisalo Juha, Skrobek Boris, Soranzo Nicole, Stan?áková Alena, Stark Klaus, Stephens Jonathan C., Stirrups Kathleen, Stolk Ronald P., Stumvoll Michael, Swift Amy J., Theodoraki Eirini V., Thorand Barbara, Tregouet David-Alexandre, Tremoli Elena, Van der Klauw Melanie M., van Meurs Joyce B.J., Vermeulen Sita H., Viikari Jorma, Virtamo Jarmo, Vitart Veronique, Waeber Gérard, Wang Zhaoming, Widén Elisabeth, Wild Sarah H., Willemsen Gonneke, Winkelmann Bernhard R., Witteman Jacqueline C.M., Wolffenbuttel Bruce H.R., Wong Andrew, Wright Alan F., Zillikens M. Carola, Amouyel Philippe, Boehm Bernhard O., Boerwinkle Eric, Boomsma Dorret I., Caulfield Mark J., Chanock Stephen J., Cupples L. Adrienne, Cusi Daniele, Dedoussis George V., Erdmann Jeanette, Eriksson Johan G., Franks Paul W., Froguel Philippe, Gieger Christian, Gyllensten Ulf, Hamsten Anders, Harris Tamara B., Hengstenberg Christian, Hicks Andrew A., Hingorani Aroon, Hinney Anke, Hofman Albert, Hovingh Kees G., Hveem Kristian, Illig Thomas, Jarvelin Marjo-Riitta, Jöckel Karl-Heinz, Keinanen-Kiukaanniemi Sirkka M., Kiemeney Lambertus A., Kuh Diana, Laakso Markku, Lehtimäki Terho, Levinson Douglas F., Martin Nicholas G., Metspalu Andres, Morris Andrew D., Nieminen Markku S., Njølstad Inger, Ohlsson Claes, Oldehinkel Albertine J., Ouwehand Willem H., Palmer Lyle J., Penninx Brenda, Power Chris, Province Michael A., Psaty Bruce M., Qi Lu, Rauramaa Rainer, Ridker Paul M., Ripatti Samuli, Salomaa Veikko, Samani Nilesh J., Snieder Harold, Sørensen Thorkild I.A., Spector Timothy D., Stefansson Kari, Tönjes Anke, Tuomilehto Jaakko, Uitterlinden André G., Uusitupa Matti, van der Harst Pim, Vollenweider Peter, Wallaschofski Henri, Wareham Nicholas J., Watkins Hugh, Wichmann H.-Erich, Wilson James F., Abecasis Goncalo R., Assimes Themistocles L., Barroso Inês, Boehnke Michael, Borecki Ingrid B., Deloukas Panos, Fox Caroline S., Frayling Timothy, Groop Leif C., Haritunian Talin, Heid Iris M., Hunter David, Kaplan Robert C., Karpe Fredrik, Moffatt Miriam, Mohlke Karen L., O’Connell Jeffrey R., Pawitan Yudi, Schadt Eric E., Schlessinger David, Steinthorsdottir Valgerdur, Strachan David P., Thorsteinsdottir Unnur, van Duijn Cornelia M., Visscher Peter M., Di Blasio Anna Maria, Hirschhorn Joel N., Lindgren Cecilia M., Morris Andrew P., Meyre David, Scherag André, McCarthy Mark I., Speliotes Elizabeth K., North Kari E., Loos Ruth J.F., Ingelsson Erik

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Nature genetics 2013; 45:501-512.

Crist RC, Ambrose-Lanci LM, Vaswani M, Clarke TK, Zeng A, Yuan C, Ferraro TN, Hakonarson H, Kampman KM, Dackis CA, Pettinati HM, O'Brien CP, Oslin DW, Doyle GA, Lohoff FW, Berrettini WH

Case-control association analysis of polymorphisms in the delta-opioid receptor, OPRD1, with cocaine and opioid addicted populations

Drug and alcohol dependence 2013; 127(1-3):122-128.

Kochunov P, Charlesworth J, Winkler A, Hong L E, Nichols T E, Curran J E, Sprooten E, Jahanshad N, Thompson P M, Johnson M P, Kent J W, Landman B A, Mitchell B, Cole S A, Dyer T D, Moses E K, Goring H H H, Almasy L, Duggirala R, Olvera R L, Glahn D C, Blangero J

Transcriptomics of cortical gray matter thickness decline during normal aging.

NeuroImage 2013; 82:273-83.

Kochunov P, Charlesworth J, Winkler A, Hong L, Nichols T, Curran J, Sprooten E, Jahanshad N, Thompson P, Johnson M, Kent J Jr, Landman B, Mitchell B, Cole S, Dyer T, Moses E, Goring H, Almasy L, Duggirala R, Olvera R, Glahn D, Blangero J

Transcriptomics of cortical gray matter thickness decline during normal aging

NeuroImage 2013; 0:273-283.

Lieber DS, Calvo SE, Shanahan K, Slate NG, Liu S, Hershman SG, Gold NB, Chapman BA, Thorburn DR, Berry GT, Schmahmann JD, Borowsky ML, Mueller DM, Sims KB, Mootha VK

Targeted exome sequencing of suspected mitochondrial disorders

Neurology 2013; 80(19):1762-1770.

Ramsey TL, Liu Q, Massey BW, Brennan MD

Genotypic variation in the SV2C gene impacts response to atypical antipsychotics the CATIE Study

Schizophrenia research 2013; 149(0):10.1016/j.schres.2013.07.008.

Ramsey Timothy L, Liu Qian, Massey Bill W, Brennan Mark D

Genotypic variation in the SV2C gene impacts response to atypical antipsychotics the CATIE study.

Schizophrenia research 2013; 149(1-3):21-5.

Talati A, Wickramaratne PJ, Keyes KM, Hasin DS, Levin FR, Weissman MM

Smoking and psychopathology increasingly associated in recent birth cohorts

Drug and alcohol dependence 2013; 133(2):10.1016/j.drugalcdep.2013.08.025.

Wang Jen-Chyong, Spiegel Noah, Bertelsen Sarah, Le Nhung, McKenna Nicholas, Budde John P, Harari Oscar, Kapoor Manav, Brooks Andrew, Hancock Dana, Tischfield Jay, Foroud Tatiana, Bierut Laura J, Steinbach Joe Henry, Edenberg Howard J, Traynor Bryan J, Goate Alison M

Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry.

PloS one 2013; 8(11):e80204.

Zuo L, Wang KS, Zhang XY, Li CS, Zhang F, Wang X, Chen W, Gao G, Zhang H, Krystal JH, Luo X

Rare SERINC2 variants are specific for alcohol dependence in subjects of European descent

Pharmacogenetics and genomics 2013; 23(8):395-402.

Zuo L, Zhang H, Malison RT, Li CS, Zhang XY, Wang F, Lu L, Lu L, Wang X, Krystal JH, Zhang F, Deng HW, Luo X

Rare ADH Variant Constellations are Specific for Alcohol Dependence

Alcohol and Alcoholism (Oxford, Oxfordshire) 2013; 48(1):9-14.

Calvo SE, Compton AG, Hershman SG, Lim SC, Lieber DS, Tucker EJ, Laskowski A, Garone C, Liu S, Jaffe DB, Christodoulou J, Fletcher JM, Bruno DL, Goldblatt J, DiMauro S, Thorburn DR, Mootha VK

Molecular Diagnosis of Infantile Mitochondrial Disease with Targeted Next-Generation Sequencing

Science translational medicine 2012; 4(118):118ra10.

Contreras J, Hare E, Escamilla M, Raventos H

Principal domains of quantitative anxiety trait in subjects with lifetime history of mania

Journal of affective disorders 2012; 136(0):e69-e75.

Dennis MY, Nuttle X, Sudmant PH, Antonacci F, Graves TA, Nefedov M, Rosenfeld JA, Sajjadian S, Malig M, Kotkiewicz H

Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication

Cell 2012; 149(4):912-922.

Karlsson R, Graae L, Lekman M, Wang D, Favis R, Axelsson T, Galter D, Belin AC, Paddock S

MAGI1 copy number variation in bipolar affective disorder and schizophrenia

Biological psychiatry 2012; 71(10):922-930.

Multani PK, Clarke TK, Narasimhan S, Ambrose-Lanci L, Kampman KM, Pettinati HM, Oslin DW, O'Brien CP, Berrettini WH, Lohoff FW

Neuronal calcium sensor-1 and cocaine addiction: A genetic association study in African-Americans and European Americans

Neuroscience letters 2012; 531(1):46-51.

Nissen S, Liang S, Shehktman T, Kelsoe JR

Evidence for Association of Bipolar Disorder to Haplotypes in the 22q12.3 Region Near the Genes Stargazin, IFT27 and Parvalbumin

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2012; 0(8):941-950.

Pasaniuc B, Rohland N, McLaren PJ, Garimella K, Zaitlen N, Li H, Gupta N, Neale BM, Daly MJ, Sklar P

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Nature genetics 2012; 44(6):631-635.

Sabunciyan S, Aryee MJ, Irizarry RA, Rongione M, Webster MJ, Kaufman WE, Murakami P, Lessard A, Yolken RH, Feinberg AP, Potash JB, Consortium G

Genome-Wide DNA Methylation Scan in Major Depressive Disorder

PLoS ONE 2012; 7(4):e34451.

Willour VL, Seifuddin F, Mahon PB, Jancic D, Pirooznia M, Steele J, Schweizer B, Goes FS, Mondimore FM, MacKinnon DF, Perlis RH, Lee PH, Huang J, Kelsoe JR, Shilling PD, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, DePaulo JR Jr, Schulze TG, McMahon FJ, Zandi PP, Potash JB

A genome-wide association study of attempted suicide

Molecular psychiatry 2012; 17(4):433-444.

Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH, Macdonald RL, Sutcliffe JS

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

Molecular psychiatry 2011; 16(1):86-96.

Hartz SM, Lin P, Edenberg HJ, Xuei X, Rochberg N, Saccone S, Berrettini W, Nelson E, Nurnberger J, Bierut LJ, Rice JP

Genetic association of bipolar disorder with the β3 nicotinic receptor subunit gene

Psychiatric genetics 2011; 21(2):77-84.

Ladouceur Roger

Devrions-nous prescrire des opioïdes pour la douleur chronique non cancéreuse?

Canadian Family Physician 2011; 57:865.

Narasimhan S, Hodge R, Doyle GA, Kraemer DJM, Prabhakaran R, Rickels K, Richardson T, Bloch PJ, Lohoff FW

Association analysis between the 5-HTTLPR polymorphism in the SLC6A4 gene and generalized anxiety disorder

Psychiatric genetics 2011; 21(5):267-268.

Peterson Roseann E, Maes Hermine H, Holmans Peter, Sanders Alan R, Levinson Douglas F, Shi Jianxin, Kendler Kenneth S, Gejman Pablo V, Webb Bradley T

Genetic risk sum score comprised of common polygenic variation is associated with body mass index.

Human genetics 2011; 129(2):221-30.

Bierut Laura J, Agrawal Arpana, Bucholz Kathleen K, Doheny Kimberly F, Laurie Cathy, Pugh Elizabeth, Fisher Sherri, Fox Louis, Howells William, Bertelsen Sarah, Hinrichs Anthony L, Almasy Laura, Breslau Naomi, Culverhouse Robert C, Dick Danielle M, Edenberg Howard J, Foroud Tatiana, Grucza Richard A, Hatsukami Dorothy, Hesselbrock Victor, Johnson Eric O, Kramer John, Krueger Robert F, Kuperman Samuel, Lynskey Michael, Mann Karl, Neuman Rosalind J, Nöthen Markus M, Nurnberger John I, Porjesz Bernice, Ridinger Monika, Saccone Nancy L, Saccone Scott F, Schuckit Marc A, Tischfield Jay A, Wang Jen C, Rietschel Marcella, Goate Alison M, Rice John P

A genome-wide association study of alcohol dependence.

Proceedings of the National Academy of Sciences of the United States of America 2010; 107(11):5082-7.

Dao DT, Mahon PB, Cai X, Kovacsics CE, Blackwell RA, Arad M, Shi J, Zandi PP, O'Donnell P, Knowles JA, Weissman MM, Coryell W, Scheftner WA, Lawson WB, Levinson DF, Thompson SM, Potash JB, Gould TD

Mood disorder susceptibility gene CACNA1C modifies mood-related behaviors in mice and interacts with sex to influence behavior in mice and diagnosis in humans

Biological psychiatry 2010; 68(9):801-810.

Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, Allen MH, Bowden CL, Calabrese JR, Fossey MD, Friedman ES, Gyulai L, Hauser P, Ketter TB, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel JK, Sachs GS, Thase ME, Molay FB, Escamilla MA, Nimgaonkar VL, Sklar P, Laird NM, Smoller JW

Linkage Disequilibrium Mapping of the Chromosome 6q21-22.31 Bipolar I Disorder Susceptibility Locus

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2010; 0(1):29-37.

Freiberg MS, Chang YF, Kraemer KL, Robinson JG, Adams-Campbell LL, Kuller LL

Liebert Librarian Resource Center

Journal of Women's Health 2010; 19(2):355-359.

Lin P, Hartz SM, Zhang Z, Saccone SF, Wang J, Tischfield JA, Edenberg HJ, Kramer JR, Goate AM, Bierut LJ

A new statistic to evaluate imputation reliability

PloS one 2010; 5(3):e9697.

Lohoff FW, Bloch PJ, Hodge R, Nall AH, Ferraro TN, Kampman KM, Dackis CA, O'Brien CP, Pettinati HM, Oslin DW

Association analysis between polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes with cocaine dependence

Neuroscience letters 2010; 473(2):87-91.

Peterson RE, Maes HH, Holmans P, Sanders AR, Levinson DF, Shi J, Kendler KS, Gejman PV, Webb BT

Genetic risk sum score comprised of common polygenic variation is associated with body mass index

Human Genetics 2010; 129(2):221-230.

Saccone N L, Schwantes-An T-H, Wang J C, Grucza R A, Breslau N, Hatsukami D, Johnson E O, Rice J P, Goate A M, Bierut L J

Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans.

Genes, brain, and behavior 2010; 9(7):741-50.

Bates JS, Lessard CJ, Leon JM, Nguyen T, Battiest LJ, Rodgers J, Kaufman KM, James JA, Gilkeson GS, Kelly JA, Humphrey MB, Harley JB, Gray-McGuire C, Moser KL, Gaffney PM

Meta-analysis and Imputation Identifies a 109 kb Risk Haplotype Spanning TNFAIP3 Associated with Lupus Nephritis and Hematologic Manifestations

Genes and immunity 2009; 10(5):470-477.

Bloch PJ, Nall AH, Weller AE, Ferraro TN, Berrettini WH, Kampman KM, Pettinati HM, Dackis CA, O'Brien CP, Oslin DW, Lohoff FW

Association analysis between polymorphisms in the dopamine D3 receptor (DRD3) gene and cocaine dependence

Psychiatric genetics 2009; 19(5):275-276.

Bukszár J, McClay JL, van den Oord EJ

Estimating the posterior probability that genome-wide association findings are true or false

Bioinformatics 2009; 25(14):1807-1813.

Le-Niculescu H, Patel SD, Bhat M, Kuczenski R, Faraone SV, Tsuang MT, McMahon FJ, Schork NJ, Nurnberger JI, Niculescu AB

Convergent functional genomics of genome-wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150(2):155-181.

Lohoff FW, Bloch PJ, Ferraro TN, Berrettini WH, Pettinati HM, Dackis CA, O'Brien CP, Kampman KM, Oslin DW

Association analysis between polymorphisms in the conserved dopamine neurotrophic factor (CDNF) gene and cocaine dependence

Neuroscience letters 2009; 453(3):199-203.

Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, KaraMohamed S, Badner JA, Matsui S, Conroy J, McQuaid D, Gergel J, Hatchwell E, Gilliam TC, Gershon ES, Nowak NJ, Dobyns WB, Cook EH Jr

Novel Submicroscopic chromosomal abnormalities detected in Autism Spectrum Disorder

Biological psychiatry 2008; 63(12):1111-1117.

Cooper JD, Smyth DJ, Smiles AM, Plagnol V, Walker NM, Allen J, Downes K, Barrett JC, Healy B, Mychaleckyj JC, Warram JH, Todd JA

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes loci

Nature genetics 2008; 40(12):1399-1401.

Foster CE, Webster MC, Weissman MM, Pilowsky DJ, Wickramaratne PJ, Talati A, Rush AJ, Hughes CW, Garber J, Malloy E, Cerda G, Kornstein SG, Alpert JE, Wisniewski SR, Trivedi MH, Fava M, King CA

Remission of Maternal Depression: Relations to Family Functioning and Youth Internalizing and Externalizing Symptoms

Journal of clinical child and adolescent psychology : the official journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53 2008; 37(4):714-724.

Liu L, Foroud T, Xuei X, Berrettini W, Byerley W, Coryell W, El-Mallakh R, Gershon ES, Kelsoe JR, Lawson WB, MacKinnon DF, McInnis M, McMahon FJ, Murphy DL, Rice J, Scheftner W, Zandi PP, Lohoff F, Niculescu AB, Meyer ET, Edenberg HJ, Nurnberger JI Jr

Evidence of association between brain-derived neurotrophic factor (BDNF) gene and bipolar disorder

Psychiatric genetics 2008; 18(6):267-274.

Takeshita M, Yamada K, Hattori E, Iwayama Y, Toyota T, Iwata Y, Tsuchiya KJ, Sugihara G, Hashimoto K, Watanabe H

Genetic examination of the PLXNA2 gene in Japanese and Chinese people with schizophrenia

Schizophrenia research 2008; 99(1):359-364.

Uhl GR, Drgon T, Johnson C, Li CY, Contoreggi C, Hess J, Naiman D, Liu QR

Molecular genetics of addiction and related heritable phenotypes: genome wide association approaches identify “connectivity constellation” and drug target genes with pleiotropic effects

Annals of the New York Academy of Sciences 2008; 1141(1):318-381.

Verma R, Holmans P, Knowles JA, Grover D, Evgrafov OV, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR Jr, Potash JB, Levinson DF

Linkage Disequilibrium Mapping of a Chromosome 15q25-26 Major Depression Linkage Region and Sequencing of NTRK3

Biological psychiatry 2008; 63(12):1185-1189.

Condra JA, Neibergs H, Wei W, Brennan MD

Evidence for two schizophrenia susceptibility genes on chromosome 22q13

Psychiatric genetics 2007; 17(5):292-298.

Francks C, Maegawa S, Laurén J, Abrahams B, Velayos-Baeza A, Medland S, Colella S, Groszer M, McAuley E, Caffrey T, Timmusk T, Pruunsild P, Koppel I, Lind P, Matsumoto-Itaba N, Nicod J, Xiong L, Joober R, Enard W, Krinsky B, Nanba E, Richardson A, Riley B, Martin N, Strittmatter S, Möller HJ, Rujescu D, St Clair D, Muglia P, Roos J, Fisher S, Wade-Martins R, Rouleau G, Stein J, Karayiorgou M, Geschwind D, Ragoussis J, Kendler K, Airaksinen M, Oshimura M, DeLisi L, Monaco A

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Molecular psychiatry 2007; 12(12):1129-1057.

Iwata Y, Nakajima M, Yamada K, Nakamura K, Sekine Y, Tsuchiya KJ, Sugihara G, Matsuzaki H, Suda S, Suzuki K

Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia

Neuroscience research 2007; 57(2):194-202.

Kerner B, Brugman DL, Freimer NB

Evidence of linkage to psychosis on chromosome 5q33-34 in pedigrees ascertained for bipolar disorder

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007; 144(1):74-78.

Nurnberger Jr JI, Kuperman S, Flury-Wetherill L, Meyer ET, Lawson WB, MacKinnon DF

Genetics of comorbid mood disorder and alcohol dependence

Journal of dual diagnosis 2007; 3(2):31-46.

Leonard S, Freedman R

Genetics of chromosome 15q13-q14 in schizophrenia

Biological psychiatry 2006; 60(2):115-122.

Schwab SG, Knapp M, Sklar P, Eckstein GN, Sewekow C, Borrmann-Hassenbach M, Albus M, Becker T, Hallmayer JF, Lerer B

Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia

Molecular psychiatry 2006; 11(9):837-846.

Mansour HA, Wood J, Chowdari KV, Dayal M, Thase ME, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL

Circadian phase variation in bipolar I disorder

Chronobiology international 2005; 22(3):571-584.

Goddard KAB, Olson JM, Payami H, van der Voet M, Kuivaniemi H, Tromp G

Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease

Neurogenetics 2004; 5(2):121-128.

Stassen HH, Bridler R, Hell D, Weisbrod M, Scharfetter C

Ethnicity-independent genetic basis of functional psychoses: A genotype-to-phenotype approach

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 124(1):101-112.

Stone WS, Faraone SV, Su J, Tarbox SI, Van Eerdewegh P, Tsuang MT

Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2004; 127(1):5-10.

Barrett TB, Hauger RL, Kennedy JL, Sadovnick AD, Remick RA, Keck PE, McElroy SL, Alexander M, Shaw SH, Kelsoe JR

Evidence that a single nucleotide polymorphism in the promoter of the G protein receptor kinase 3 gene is associated with bipolar disorder

Molecular psychiatry 2003; 8(5):546-557.

Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24

Molecular psychiatry 2003; 8(5):488-498.

Stopkova P, Saito T, Fann CSJ, Papolos DF, Vevera J, Paclt I, Zukov I, Stryjer R, Strous RD, Lachman HM

Polymorphism Screening of PIP5K2A: A Candidate Gene for Chromosome 10p-Linked Psychiatric Disorders

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 123(1):50-58.

Willour VL, Zandi PP, Huo Y, Diggs TL, Chellis JL, MacKinnon DF, Simpson SG, McMahon FJ, Potash JB, Gershon ES

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 121(1):21-27.

Zandi PP, Willour VL, Huo Y, Chellis J, Potash JB, MacKinnon DF, Simpson SG, McMahon FJ, Gershon E, Reich T

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2003; 119(1):69-76.

Bassett SS, Avramopoulos D, Fallin D

Evidence for parent of origin effect in late-onset Alzheimer disease

American journal of medical genetics 2002; 114(6):679-686.

Chowdari KV, Mirnics K, Semwal P, Wood J, Lawrence E, Bhatia T, Deshpande SN, Thelma BK, Ferrell RE, Middleton FA

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

Human molecular genetics 2002; 11(12):1373-1380.

Ohtsuki T, Ishiguro H, Detera-Wadleigh SD, Toyota T, Shimizu H, Yamada K, Yoshitsugu K, Hattori E, Yoshikawa T, Arinami T

Association between serotonin 4 receptor gene polymorphisms and bipolar disorder in Japanese case-control samples and the NIMH Genetics Initiative Bipolar Pedigrees

Molecular psychiatry 2002; 7(9):954-961.

Olson JM

Mixture models for linkage analysis of affected sibling pairs with covariates

Genetic epidemiology 2002; 23(4):444-448.

Wilcox MA, Faraone SV, Su J, Van Eerdewegh P, Tsuang MT

Genome scan of three quantitative traits in schizophrenia pedigrees

Biological psychiatry 2002; 52(9):847-854.

Torres R, Leroy E, Hu X, Katrivanou A, Gourzis P, Papachatzopoulou A, Athanassiadou A, Beratis S, Collier D, Polymeropoulos MH

Mutation screening of the Wolfram syndrome gene in psychiatric patients

Molecular psychiatry 2001; 6(1):39-43.

Bertram L, Blacker D, Mullin K, Keeney D, Jones J, Basu S, Yhu S, McInnis MG, Go RCP, Vekrellis K

Evidence for genetic linkage of Alzheimer's disease to chromosome 10q

Science 2000; 290(5500):2302-2303.

Adler LE, Freedman R, Ross RG, Olincy A, Waldo MC

Elementary phenotypes in the neurobiological and genetic study of schizophrenia

Biological psychiatry 1999; 46(1):8-18.

Austin CP, Holder DJ, Ma L, Mixson LA, Caskey CT

Mapping of hKCa3 to chromosome 1q21 and investigation of linkage of CAG repeat polymorphism to schizophrenia

Molecular psychiatry 1999; 4(3):261-266.

Nurnberger JI, Trofatter J, Mayeda A, Tarricone B, Hofstetter J, Simon J, Grahame N, Lahiri DK, Belknap J, Hingtgen J

Quantitative trait loci for traits related to affective disorder in inbred strains of mice

American Journal of Medical Genetics Part B Neuropsychiatric Genetics 1998; 81(6):472.