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
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.
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 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.
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.
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.
Sullivan PF
The psychiatric GWAS consortium: big science comes to psychiatry
Neuron 2010; 68(2):182-186.
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 of the United States of America 2016; 113(19):5418-5423.
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.
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, 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.
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.
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.
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
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arXiv preprint arXiv:1209.2911 2012
Agrawal A, Nurnberger JI Jr, Lynskey MT
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Alliey-Rodriguez N, Zhang D, Badner JA, Lahey BB, Zhang X, Dinwiddie S, Romanos B, Plenys N, Liu C, Gershon ES
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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.
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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.
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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
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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
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Neuron 2011; 72(4):545-58.
Singh KK, DiRienzo G, Drane L, Mao Y, Flood Z, Madison J, Ferreira M, Bergen S, King C, Sklar P, Sive H, Tsai LH
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Neuron 2011; 72(4):545-558.
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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
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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
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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
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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
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Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients
The American journal of psychiatry 2010; 167(12):1499-1507.
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Neuron 2010; 68(2):182-186.
Zhang P, Xiang N, Chen Y, Œliwerska E, McInnis MG, Burmeister M, Zöllner S
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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
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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
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Hoffmann TJ, Lange C, Vansteelandt S, Laird NM
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Genetic epidemiology 2009; 33(8):691-699.
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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
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American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2009; 150B(1):24-32.
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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
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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
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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
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Dialogues in Clinical Neuroscience 2008; 10(2):141-152.
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.
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.
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, 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.
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.
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
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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
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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.
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Linked gene ontology categories are novel and differ from associated gene ontology categories for the bipolar disorders
Psychiatric genetics 2007; 17(1):29-34.
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
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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.
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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.
Howrigan DP, Simonson MA, Keller MC
Detecting autozygosity through runs of homozygosity: A comparison of three autozygosity detection algorithms
BMC Genomics 2011; 12:460.
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.
Gershon ES
Bipolar illness and schizophrenia as oligogenic diseases: implications for the future
Biol Psychiatry 2005; 47:240-244.
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.
Badner JA, Gershon ES
Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7
Mol Psychiatry 2002; 7:56-66.
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.
Kaiser Roselinde H, Chase Henry W, Phillips Mary L, Deckersbach Thilo, Parsey Ramin V, Fava Maurizio, McGrath Patrick J, Weissman Myrna, Oquendo Maria A, McInnis Melvin G, Carmody Thomas, Cooper Crystal M, Trivedi Madhukar H, Pizzagalli Diego A
Dynamic Resting-State Network Biomarkers of Antidepressant Treatment Response.
Biological psychiatry 2022; 92(7):533-542.
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.
Medeiros GC, Rush AJ, Jha M, Carmody T, Furman JL, Czysz AH, Trombello JM, Cooper CM, Trivedi MH
Positive and negative valence systems in major depression have distinct clinical features, response to antidepressants and relationships with immunomarkers
Depression and anxiety 2020; 37(8):771-783.
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.
Jha MK, Minhajuddin A, Gadad BS, Chin Fatt C, Trivedi MH
Higher S100B Levels Predict Persistently Elevated Anhedonia with Escitalopram Monotherapy Versus Antidepressant Combinations: Findings from CO-MED Trial
Pharmaceuticals 2019; 12(4):184.
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.
Graae L, Karlsson R, Paddock S
Significant Association of Estrogen Receptor Binding Site Variation with Bipolar Disorder in Females
PLoS ONE 2012; 7(2):e32304.
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.
Sullivan PF
The psychiatric GWAS consortium: big science comes to psychiatry
Neuron 2010; 68(2):182-186.
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
Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, McDaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, Mulle JG, Duan J
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons
American Journal of Human Genetics 2022; 109(8):1500-1519.
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.
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.
Panchision DM
Progress and challenges in using human stem cells for biological and therapeutics discovery: neuropsychiatric disorders
Stem cells (Dayton, Ohio) 2016; 34(3):523-536.
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-.
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.
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 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.
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.
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
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American Journal of Psychiatry 2011
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GALC Deletions Increase the Risk of Primary Open-Angle Glaucoma: The Role of Mendelian Variants in Complex Disease
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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
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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, 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.
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.
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.
Kohn Y, Lerer B
Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm
Molecular psychiatry 2005; 10(12):1062-1073.
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.
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.
Gershon ES, Badner JA
Incorporation of molecular data and redefinition of phenotype: new approaches to genetic epidemiology of bipolar manic depressive illness and schizophrenia
Dialogues in Clinical Neuroscience 2001; 3(1):63-71.
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.
DeLisi LE
Critical overview of current approaches to genetic mechanisms in schizophrenia research
Brain Research Reviews 2000; 31(2):187-192.
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, 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.
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.
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
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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.
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Uncategorized
Chiêm B, Abbas K, Amico E, Duong-Tran DA, Crevecoeur F, Goñi J
Improving Functional Connectome Fingerprinting with Degree-Normalization
Brain Connectivity 2022; 12(2):180-192.
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 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:.
Ali AT, Boehme L, Carbajosa G, Seitan VC, Small KS, Hodgkinson A
Nuclear genetic regulation of the human mitochondrial transcriptome
eLife 2019; 8:e41927.
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
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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
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Polygenic risk score for schizophrenia is not strongly associated with the expression of specific genes or gene sets.
Psychiatr Genet 2018; 28:4.
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.
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.
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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.
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JAMA Psychiatry 2018; 75:9.
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