Supplementary Note Acknowledgments by Phenotype Alcohol-Related Problems
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Supplementary Note Acknowledgments by Phenotype Alcohol-Related Problems (Young Adults) – Avon Longitudinal Study of Parents and Children (ALSPAC). We graciously thank Kenneth Kendler, Alexis Edwards, and the Avon Longitudinal Study of Parents and Children, for the generous provision of GWAS summary data. We are extremely grateful to all the families who took part in this study, the midwives for their help in recruiting them, and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses. The UK Medical Research Council and the Wellcome Trust (Grant refs: 092731 and 074268/Z/07/Z) and the University of Bristol provide core support for ALSPAC. GWAS data was generated by Sample Logistics and Genotyping Facilities at the Wellcome Trust Sanger Institute and LabCorp (Laboratory Corporation of America) using support from 23andMe. Alzheimer’s disease – International Genomics of Alzheimer's Project (IGAP) We thank the International Genomics of Alzheimer's Project (IGAP) for providing summary results data for these analyses. The investigators within IGAP contributed to the design and implementation of IGAP and/or provided data but did not participate in analysis or writing of this report. IGAP was made possible by the generous participation of the control subjects, the patients, and their families. The i–Select chips was funded by the French National Foundation on Alzheimer's disease and related disorders. EADI was supported by the LABEX (laboratory of excellence program investment for the future) DISTALZ grant, Inserm, Institut Pasteur de Lille, Université de Lille 2 and the Lille University Hospital. GERAD was supported by the Medical Research Council (Grant n° 503480), Alzheimer's Research UK (Grant n° 503176), the Wellcome Trust (Grant n° 082604/2/07/Z) and German Federal Ministry of Education and Research (BMBF): Competence Network Dementia (CND) grant n° 01GI0102, 01GI0711, 01GI0420. CHARGE was partly supported by the NIH/NIA grant R01 AG033193 and the NIA AG081220 and AGES contract N01–AG–12100, the NHLBI grant R01 HL105756, the Icelandic Heart Association, and the Erasmus Medical Center and Erasmus University. ADGC was supported by the NIH/NIA grants: U01 AG032984, U24 AG021886, U01 AG016976, and the Alzheimer's Association grant ADGC–10–196728. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Lambert JC, Ibrahim-Verbaas CA, Harold D, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat Genet. 2013;45(12):1452-1458. doi:10.1038/ng.2802.
We graciously thank Eric Mick, colleagues, and collaborators for the generous provision of two sets of GWAS summary data related to aspects of angry temperament. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Mick E, McGough J, Deutsch CK, Frazier JA, Kennedy D, Goldberg RJ. Genome-wide association study of proneness to anger. PLoS One. 2014;9(1):e87257. doi:10.1371/journal.pone.0087257.
We graciously thank the Anxiety Neuro Genetics STudy for the generous provision of GWAS meta-analysis summary data, made freely available (https://www.med.unc.edu/pgc/results-and-downloads). This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Otowa T, Hek K, Lee M, et al. Meta-analysis of genome-wide association studies of anxiety disorders. Mol Psychiatry. January 2016. doi:10.1038/mp.2015.197.
We graciously thank the EArly Genetics and Lifecourse Epidemiology (EAGLE) eczema consortium, for their generous contribution of GWAS meta-analysis summary level data. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium, Australian Asthma Genetics Consortium (AAGC), Australian Asthma Genetics Consortium AAGC. Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nat Genet. 2015;47(12):1449-1456. doi:10.1038/ng.3424.
We graciously thank the Attention‐Deficit Hyperactivity Disorder Working Group of the Psychiatric Genomics Consortium for the generous provision of GWAS meta-analysis summary data, made freely available (https://www.med.unc.edu/pgc/results-and-downloads). A full listing of the Working Group authors is provided in the subsequent section. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: 1. Neale BM, Medland SE, Ripke S, et al. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2010;49(9):884-897. doi:10.1016/j.jaac.2010.06.008.
We graciously thank the Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium for the generous provision of GWAS meta-analysis summary data, which are freely available (https://www.med.unc.edu/pgc/results-and-downloads). This study utilized data generated from numerous sites, each with their own unique support mechanisms. Full acknowledgments and support mechanisms for these data have not yet been published, but a full listing of Working Group authors is provided in the subsequent section. Autoimmune Hepatitis – de Boer et al., 2014 We graciously thank Lude Franke, Gerd Bouma, and their colleagues and collaborators for the generous provision of autoimmune hepatitis GWAS meta-analysis summary data. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: De Boer YS, Van Gerven NMF, Zwiers A, et al. Genome-wide association study identifies variants associated with autoimmune hepatitis type 1. Gastroenterology. 2014;147(2). doi:10.1053/j.gastro.2014.04.022.
We graciously thank the Bipolar Disorders Working Group of the Psychiatric Genomics Consortium for the generous provision of GWAS meta-analysis summary data, made freely available (https://www.med.unc.edu/pgc/results-and-downloads). A full listing of the Working Group authors is provided in the subsequent section. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet. 2011;43(10):977-983. doi:10.1038/ng.943.
We graciously thank the Early Growth Genetics Consortium for the generous provision of birth weight and birth length GWAS meta-analysis summary data, which are shared freely (www.egg-consortium.org). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publications: Horikoshi M, Yaghootkar H, Mook-Kanamori DO, et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat Genet. 2013;45(1):76-82. doi:10.1038/ng.2477.
We graciously thank the International Consortium for Blood Pressure Genome-Wide Association Studies for the generous provision of 4 sets of GWAS meta-analysis summary level data. Data were obtained via the Database of Genotypes and Phenotypes (dbGaP; accession phs000585.v1.p1). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publications: Ehret GB, Munroe PB, Rice KM, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011;478(7367):103-109. doi:10.1038/nature10405. Wain L V, Verwoert GC, O’Reilly PF, et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet. 2011;43(10):1005-1011. doi:10.1038/ng.922. Borderline Personality Disorder - Netherlands Twin Register and The Netherlands Study of Depression and Anxiety. We graciously thank Dorret Boomsma, Gitta Lubke, and the Netherlands Twin Register and Study of Depression and Anxiety, for their generous provision of borderline personality disorder GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Lubke GH, Laurin C, Amin N, et al. Genome-wide analyses of borderline personality features. Mol Psychiatry. 2014;19(8):923-929. doi:10.1038/mp.2013.109.
We graciously thank David A. van Heel, colleagues, and collaborators for the generous provision of celiac disease GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Dubois PCA, Trynka G, Franke L, et al. Multiple common variants for celiac disease influencing immune gene expression. Nat Genet. 2010;42(4):295-302. doi:10.1038/ng.543.
We graciously thank Andrew Crawford, Brian Walker, and the CORtisol NETwork Consortium, for the generous provision of morning cortisol GWAS meta-analysis summary data. The consortium coordination is supported by the Scottish Government Chief Scientist Office, British Heart Foundation and Wellcome Trust. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Bolton JL, Hayward C, Direk N, et al. Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. PLoS Genet. 2014;10(7):e1004474. doi:10.1371/journal.pgen.1004474.
We graciously thank the International Inflammatory Bowel Disease Genetics Consortium for the generous provision of Crohn’s disease GWAS meta-analysis summary data, which are freely available (http://www.ibdgenetics.org/downloads.html). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Franke A, McGovern DPB, Barrett JC, et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci. Nat Genet. 2010;42(12):1118-1125. doi:10.1038/ng.717.
We graciously thank the CARDIoGRAM plus C4D for the generous provision of coronary artery disease GWAS meta-analysis summary data. Data on coronary artery disease myocardial infarction have been contributed by CARDIoGRAMplusC4D investigators and have been downloaded from www.CARDIOGRAMPLUSC4D.ORG. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Schunkert H, König IR, Kathiresan S, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011;43(4):333-338. doi:10.1038/ng.784.
We graciously thank Patrick Sleiman, Hakon Hakonarson, and their colleagues and collaborators for the generous provision of eosinophilic esophagitis GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Sleiman PMA, Wang M-L, Cianferoni A, et al. GWAS identifies four novel eosinophilic esophagitis loci. Nat Commun. 2014;5:5593. doi:10.1038/ncomms6593.
We graciously thank Sanjay Sisodiya, colleagues, and collaborators for the generous provision of epilepsy (partial seizures) GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Kasperaviciūte D, Catarino CB, Heinzen EL, et al. Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Brain. 2010;133(Pt 7):2136-2147. doi:10.1093/brain/awq130.
We graciously thank Katherine Siminovitch, collegues, and collaborators for the generous provision of granulomatosis with polyangitis GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Xie G, Roshandel D, Sherva R, et al. Association of granulomatosis with polyangiitis (Wegener’s) with HLA-DPB1*04 and SEMA6A gene variants: Evidence grom genome-wide analysis. Arthritis Rheum. 2013;65(9):2457-2468. doi:10.1002/art.38036.
We graciously thank the Early Growth Genetics Consortium for the generous provision of head circumference GWAS meta-analysis summary data, which are shared freely (www.egg-consortium.org). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Taal HR, St Pourcain B, Thiering E, et al. Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat Genet. 2012;44(5):532-538. doi:10.1038/ng.2238.
We graciously thank Bruce Walker, Paul de Bakker, Paul McLaren, and the members of the consortium that carried out The International HIV Controllers Study, for the generous provision of GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: The International HIV Controllers Study. The Major Genetic Determinants of HIV-1 Control Affect HLA Class I Peptide Presentation. Science (80- ). 2010;330(6010):1551-1557. doi:10.1126/science.1195271.
We graciously thank Andrew Levine for assistance in coordinating permissions and data transfer. We thank the Multicenter AIDS Cohort Study (MACS) for the generous provision of GWAS meta-analysis summary data. Data in this manuscript were collected by the Multicenter AIDS Cohort Study (MACS) with centers at Baltimore (U01-AI35042): The Johns Hopkins University Bloomberg School of Public Health: Joseph B. Margolick (PI), Jay Bream, Todd Brown, Barbara Crain, Adrian Dobs, Michelle Estrella, W. David Hardy, Lisette Johnson-Hill, Sean Leng, Anne Monroe, Cynthia Munro, Michael W. Plankey, Wendy Post, Ned Sacktor, Jennifer Schrack, Chloe Thio; Chicago (U01-AI35039): Feinberg School of Medicine, Northwestern University, and Cook County Bureau of Health Services: Steven M. Wolinsky (PI), John P. Phair, Sheila Badri, Dana Gabuzda, Frank J. Palella, Jr., Sudhir Penugonda, Susheel Reddy, Matthew Stephens, Linda Teplin; Los Angeles (U01-AI35040): University of California, UCLA Schools of Public Health and Medicine: Roger Detels (PI), Otoniel Martínez-Maza (Co-P I), Aaron Aronow, Peter Anton, Robert Bolan, Elizabeth Breen, Anthony Butch, Shehnaz Hussain, Beth Jamieson, Eric N. Miller, John Oishi, Harry Vinters, Dorothy Wiley, Mallory Witt, Otto Yang, Stephen Young, Zuo Feng Zhang; Pittsburgh (U01-AI35041): University of Pittsburgh, Graduate School of Public Health: Charles R. Rinaldo (PI), Lawrence A. Kingsley (Co-PI), James T. Becker, Phalguni Gupta, Kenneth Ho, Susan Koletar, Jeremy J. Martinson, John W. Mellors, Anthony J. Silvestre, Ronald D. Stall; Data Coordinating Center (UM1-AI35043): The Johns Hopkins University Bloomberg School of Public Health: Lisa P. Jacobson (PI), Gypsyamber D’Souza (Co-PI), Alison, Abraham, Keri Althoff, Jennifer Deal, Priya Duggal, Sabina Haberlen, Eithne Keelagan, Alvaro Muñoz , Derek Ng, Eric C. Seaberg, Sol Su, Pamela Surkan. Institute of Allergy and Infectious Diseases: Robin E. Huebner; National Cancer Institute: Geraldina Dominguez. The MACS is funded primarily by the National Institute of Allergy and Infectious Diseases (NIAID), with additional co-funding from the National Cancer Institute (NCI), the National Institute on Drug Abuse (NIDA), and the National Institute of Mental Health (NIMH). Targeted supplemental funding for specific projects was also provided by the National Heart, Lung, and Blood Institute (NHLBI), and the National Institute on Deafness and Communication Disorders (NIDCD). MACS data collection is also supported by UL1-TR001079 (JHU ICTR) from the National Center for Advancing Translational Sciences (NCATS) a component of the National Institutes of Health (NIH), and NIH Roadmap for Medical Research. The contents of this publication are solely the responsibility of the authors and do not represent the official views of the National Institutes of Health (NIH), Johns Hopkins ICTR, or NCATS. The MACS website is located at http://aidscohortstudy.org/. Acknowledgments specific to the study of HIV-associated neurocognitive impairment and dementia can be found in the following publication: Levine AJ, Service S, Miller EN, et al. Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. Am J Med Genet B Neuropsychiatr Genet. 2012;159B(6):669-683. doi:10.1002/ajmg.b.32071. IgA Nephropathy – Kiryluk et al., 2014. We graciously thank Krzysztof Kiryluk, colleagues, and collaborators for the generous provision of IgA nephropathy GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Kiryluk K, Li Y, Scolari F, et al. Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. Nat Genet. 2014;46(11):1187-1196. doi:10.1038/ng.3118.
We graciously thank M. Arfan Ikram, the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, and more specifically, the neuroCHARGE Working Group for the generous provision of intracranial volume GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Ikram MA, Fornage M, Smith A V, et al. Common variants at 6q22 and 17q21 are associated with intracranial volume. Nat Genet. 2012;44(5):539-544. doi:10.1038/ng.2245.
We graciously thank the METASTROKE Consortium of the International Stroke Genetics Consortium, for the provision of 4 sets of stroke GWAS meta-analysis summary statistics. A full listing of METASTROKE authors is provided in the following section. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Traylor M, Farrall M, Holliday EG, et al. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): A meta-analysis of genome-wide association studies. Lancet Neurol. 2012;11(11):951-962. doi:10.1016/S1474-4422(12)70234-X.
We graciously thank the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium for the generous provision of GWAS meta-analysis summary data, made freely available (https://www.med.unc.edu/pgc/results-and-downloads). A full listing of the Working Group authors is provided in the subsequent section. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Ripke S, Wray NR, Lewis CM, et al. A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry. 2013;18(4):497-511. doi:10.1038/mp.2012.21.
We graciously thank Nicholas Cross, colleagues, and collaborators for the generous provision of myeloid neoplasm GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Tapper W, Jones A V., Kralovics R, et al. Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Nat Commun. 2015;6:6691. doi:10.1038/ncomms7691.
We graciously thank the Obsessive Compulsive Disorder and Tourette Syndrome Working Group of the Psychiatric Genomics Consortium for the provision of two sets of GWAS meta-analysis summary data related to these phenotypes. Their study utilized data generated from numerous sites, each with their own unique support mechanisms. Full acknowledgments and support mechanisms for these data have not yet been published, but a full listing of Working Group authors is provided in the subsequent section. Otitis Media (Chronic) - Western Australian Pregnancy Cohort (Raine) Study We graciously thank the Western Australian Pregnancy Cohort (Raine) Study for the generous provision of chronic otitis media GWAS summary statistics. Full acknowledgment and support for this study can be found in the following publication: Rye MS, Warrington NM, Scaman ESH, et al. Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood. PLoS One. 2012;7(10):e48215. doi:10.1371/journal.pone.0048215.
We graciously thank the Genetics of Personality Consortium for the generous provision of 5 sets of GWAS meta-analysis summary statistics related to personality domains, which are provided freely (http://www.tweelingenregister.org/GPC/). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: de Moor MHM, Costa PT, Terracciano A, et al. Meta-analysis of genome-wide association studies for personality. Mol Psychiatry. 2012;17(3):337-349. doi:10.1038/mp.2010.128.
We graciously thank Eva Ellinghaus, colleagues, and collaborators for the generous provision of psoriatic arthritis GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Ellinghaus E, Stuart PE, Ellinghaus D, et al. Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL. J Invest Dermatol. 2012;132(4):1133-1140. doi:10.1038/jid.2011.415.
We graciously thank Jeffrey Gruen, the Avon Longitudinal Study of Parents and Children (ALSPAC), and the Pediatric Imaging, Neurocognition and Genetics Study (PING), for the generous provision of 3 sets of GWAS summary data. We are extremely grateful to all the families who took part in this study, the midwives for their help in recruiting them, and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses. The UK Medical Research Council and the Wellcome Trust (Grant refs: 092731 and 074268/Z/07/Z) and the University of Bristol provide core support for ALSPAC. GWAS data was generated by Sample Logistics and Genotyping Facilities at the Wellcome Trust Sanger Institute and LabCorp (Laboratory Corporation of America) using support from 23andMe. These data used in the present study were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publications: Eicher JD, Powers NR, Miller LL, et al. Genome-wide association study of shared components of reading disability and language impairment. Genes Brain Behav. 2013;12(8):792-801. doi:10.1111/gbb.12085. Jernigan TL, Brown TT, Hagler DJ, et al. The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. Neuroimage. 2016;124(Pt B):1149-1154. doi:10.1016/j.neuroimage.2015.04.057.
We graciously thank Yukinori Okada, colleagues, and collaborators for the generous provision of rheumatoid arthritis GWAS summary data, which are freely available (http://plaza.umin.ac.jp/yokada/datasource/software.htm). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Okada Y, Wu D, Trynka G, et al. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature. 2014;506(7488):376-381. doi:10.1038/nature12873.
We graciously thank Annegret Fischer, colleagues, and collaborators for the generous provision of sarcoidosis GWAS summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Hofmann S, Fischer A, Nothnagel M, et al. Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. Eur Respir J. 2013;41(4):888-900. doi:10.1183/09031936.00033812.
We graciously thank the Schizophrenia Working Group of the Psychiatric Genomics Consortium for the generous provision of GWAS meta-analysis summary data, made freely available (https://www.med.unc.edu/pgc/results-and-downloads). A full listing of the Working Group authors is provided in the subsequent section. This study utilized data generated from numerous sites, each with their own unique support mechanisms, identified in the following publication: Ripke S, Neale BM, Corvin A, et al. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 2014;511(7510):421-427. doi:10.1038/nature13595.
We graciously thank Joel Gelernter, Richard Sherva, and their colleagues and collaborators for the generous provision of 4 sets of GWAS meta-analysis summary statistics related to alcohol, cocaine, and opioid dependence. These data were generated from combined efforts distributed across several sites, each with unique support mechanisms, identified in the following publications: Gelernter J, Kranzler HR, Sherva R, et al. Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. Mol Psychiatry. 2014;19(1):41-49. doi:10.1038/mp.2013.145. Gelernter J, Sherva R, Koesterer R, et al. Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. Mol Psychiatry. 2014;19(6):717-723. doi:10.1038/mp.2013.99. Gelernter J, Kranzler HR, Sherva R, et al. Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways. Biol Psychiatry. 2014;76(1):66-74. doi:10.1016/j.biopsych.2013.08.034.
The data used for the analyses described in this paper were obtained from the database of Genotypes and Phenotypes (dbGaP), at http://www.ncbi.nlm.nih.gov/gap. Genotype and phenotype data for the Whole Genome Association Study of Systemic Lupus Erythematosus (dbGaP accession number phs000122.v1.p1) were provided by Timothy W. Behrens, Peter K. Gregersen, Lindsey Criswell, and Susan Manzi. Funding support for the original study was provided by Genentech, the National Institutes of Health, and other sources as detailed in Hom G, et al. Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. N Engl J Med. 2008. 358(9):900-9. Systemic Sclerosis / Scleroderma – Radstake et al., 2010 We graciously thank Timothy Radstake, Maureeen Mayes, and their colleagues, and collaborators for the generous provision of systemic sclerosis GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Radstake TRDJ, Gorlova O, Rueda B, et al. Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Nat Genet. 2010;42(5):426-429. doi:10.1038/ng.565.
We graciously thank the Tobacco and Genetics Consortium for the generous provision of two sets of GWAS summary data related to smoking behavior; these data are provided freely (https://www.med.unc.edu/pgc/results-and-downloads). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Nat Genet. 2010;42(5):441-447. doi:10.1038/ng.571.
We graciously thank Sergey Nejentsev, Jeffrey Barrett, Doug Speed, and their colleagues and collaborators for the generous provision of pulmonary tuberculosis GWAS summary data. Doug Speed was funded by the Medical Research Council under grant MR/L012561/1. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Curtis J, Luo Y, Zenner HL, et al. Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration. Nat Genet. 2015;47(5):523-527. doi:10.1038/ng.3248.
We graciously thank Jonathan Bradfield, Constantin Polychronakos, Hakon Hakonarson, and their colleagues and collaborators for the generous provision of type 1 diabetes GWAS meta-analysis summary data. These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Bradfield JP, Qu HQ, Wang K, et al. A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. PLoS Genet. 2011;7(9). doi:10.1371/journal.pgen.1002293.
We graciously thank the DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium for the generous provision of type 2 diabetes GWAS meta-analysis summary data (DIAGRAM v3), which are provided freely (http://diagram-consortium.org/downloads.html). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Morris AP, Voight BF, Teslovich TM, et al. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet. 2012;44(9):981-990. doi:10.1038/ng.2383.
We graciously thank the International Inflammatory Bowel Disease Genetics Consortium for the generous provision of ulcerative colitis GWAS meta-analysis summary data, which are freely available (http://www.ibdgenetics.org/downloads.html). These data were generated from combined efforts distributed across numerous sites, each with unique support mechanisms, identified in the following publication: Anderson CA, Boucher G, Lees CW, et al. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet. 2011;43(3):246-252. doi:10.1038/ng.764.
Stephen Faraone, Bru Cormand, Josep Antoni Ramos‐Quiroga, Cristina Sánchez‐Mora, Marta Ribasés, Miguel Casas, Mònica Bayés, Amaia Hervas, Maria Jesús Arranz, Yufeng Wang, Jan Haavik, Tetyana Zayats, Stefan Johansson, Carol A. Mathews, Nigel Williams, Peter Holmans, Joanna Martin, Hakon Hakonarson, Josephine Elia, Tobias J Renner, Nguyen Trang, Benno G Schimmelmann, Anke Hinney, Özgür Albayrak, Anna‐Lena Volckmar, Johannes Hebebrand, André Scherag, Astrid Dempfle, Beate Herpertz‐Dahlmann, Judith Sinzig, Gerd Lehmkuhl, Aribert Rothenberger, Edmund J S Sonuga‐Barke, Hans‐Christoph Steinhausen, Jonna Kuntsi, Philip Asherson, Robert D. Oades, Tobias Banaschewski, Ana Miranda, Fernando Mulas, Herbert Roeyers, Joseph Sergeant, Richard P. Ebstein, Tobias J. Banaschewski, Sarah Hohmann, Tobias J Renner, Helmut Schäfer, Barbara Franke, Jan K. Buitelaar, Lindsey Kent, Alejandro Arias Vasquez, Michael Gill, Nanda Lambregts‐Rommelse, Richard JL Anney, Aisling Mulligan, Joseph Biederman, Stephen V. Faraone, Yanli Zhang‐James, Alysa E. Doyle, Andreas Reif, Klaus‐Peter Lesch, Andreas Warnke, Christine Freitag, Jasmin Romanos, Susanne Walitza, Olga Rivero, Haukur Palmason, Jobst Meyer, Marcel Romanos, Anita Thapar, Kate Langley, Michael C. O’Donovan, Michael J. Owen, Marcella Rietschel , Stephanie H Witt, Soeren Dalsgaard, Preben Bo Mortensen, Anders Børglum, Ditte Demontis, Joel Gelernter, Irwin Waldman, Joel Nigg, Beth Wilmot, Nikolas Molly , McWeeney Shannon , Luis Rhode, Claiton Bau, Mara Hutz, Nina Roth Mota, Alexandre Todorov, Eric Mick, Sarah E. Medland, Benjamin M Neale, Raymond Walters, Mark J. Daly, Stephan Ripke, Alice Charach, Jennifer Crosbie, Russell Schachar, Abel Ickowitz, Jennifer Crosbie, Sandra K. Loo, Stan F. Nelson, Susan L. Smalley and James J. McGough Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium Richard Anney, Stephan Ripke, Verneri Anttila, Peter Holmans, Hailiang Huang, Lambertus Klei, Phil Lee, Sarah Medland, Benjamin Neale, Elise Robinson, Lauren Weiss, Joana Almeida, David Amaral, Evdokia Anagnostou, Elena Bacchelli, Joel Bader, Anthony Bailey, Gillian Baird, Vanessa Bal, Agatino Battaglia, Arthur Beaudet, Raphael Bernier, Catalina Betancur, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, Sean Brennan, Cátia Café, Rita Cantor, Jillian Casey, Patrícia Celestino‐Soper, Andreas Chiocchetti, Ines Conceição, Judith Conroy, Catarina Correia, Michael Cuccaro, Geraldine Dawson, Maretha De Jonge, Silvia De Rubeis, Richard Delorme, Eftichia Duketis, Frederico Duque, Sean Ennis, A. Gulhan Ercan‐Sencicek, M. Daniele Fallin, Bridget Fernandez, Susan Folstein, Eric Fombonne, Christine Freitag, Louise Gallagher, John Gilbert, Christopher Gillberg, Arthur Goldberg, Jonathan Green, Andrew Green, Dorothy Grice, Stephen Guter, Jonathan Haines, Robert Hendren, Irva Hertz‐Picciotto, Christina Hultman, Bozenna Iliadou, Suma Jacob, Sabine Klauck, Alexander Kolevzon, Christine Ladd‐Acosta, Ann Le Couteur, Marion Leboyer, David Ledbetter, Christa Lese Martin, Pat Levitt, Catherine Lord, Jennifer Lowe, Elena Maestrini, Tiago Magalhaes, Pall Magnusson, Shrikant Mane, Donna Martin, Igor Martsenkovsky, Susan McGrew, William McMahon, Alison Merikangas, Nancy Minshew, Anthony Monaco, Daniel Moreno‐De‐Luca, Eric Morrow, Susana Mouga, Michael Murtha, John Nurnberger, Guiomar Oliveira, Alistair Pagnamenta, Jeremy Parr, Andrew Paterson, Milica Pejovic Milovancevic, Margaret Pericak‐Vance, Dalila Pinto, Joseph Piven, Christopher Poultney, Fritz Poustka, Regina Regan, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Wendy Roberts, Kathryn Roeder, Bernadette Rogé, Guy Rouleau, Evald Saemundsen, Stephan Sanders, Sven Sandin, Gerard Schellenberg, Stephen Scherer, Teimuraz Silagadze, Latha Soorya, Matthew State, Hreinn Stefansson, Kari Stefansson, Stacy Steinberg , Oscar Svantesson, Peter Szatmari, Ann Thompson, Kathryn Tsang, Herman van Engeland, Astrid Vicente, Veronica Vieland, Jacob Vorstman, Simon Wallace, Christopher Walsh, Regina Waltes, Thomas Wassink, Ellen Wijsman, A. Jeremy Willsey, Kerstin Wittemeyer, Timothy Yu, Lonnie Zwaigenbaum, Joseph Buxbaum, Aravinda Chakravarti, Edwin Cook, Hilary Coon, Daniel Geschwind, Michael Gill, Hakon Hakonarson, Joachim Hallmayer, Aarno Palotie, Susan Santangelo, James Sutcliffe, Dan Arking, Bernie Devlin and Mark Daly Bipolar Disorders Working Group of the Psychiatric Genomics Consortium René Breuer, Marcella Rietschel, Thomas G Schulze, Jana Strohmaier, Stephanie H Witt, Anne Farmer, Peter McGuffin, John Strauss, Wei Xu, James L Kennedy, John B Vincent, Keith Matthews, Manuel Ferreira, Roy Perlis, Colm O'Dushlaine, Shaun Purcell, Soumya Raychaudhuri, Douglas Ruderfer, Pamela Sklar, Jordan Smoller, Laura J Scott, Matthew Flickinger, Margit Burmeister, Jun Li, Weihua Guan, Devin Absher, Robert C Thompson, Fan Guo Meng, Alan F Schatzberg, William E Bunney, Jack D Barchas, Stanley J Watson, Richard M Myers, Huda Akil, Michael Boehnke, Kim Chambert, Jennifer Moran, Ed Scolnick, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Gunnar Morken, Aiden Corvin, Michael Gill, Derek Morris, Emma Quinn, Adebayo Anjorin, Nick Bass, Hugh Gurling, Radhika Kandaswamy, Jacob Lawrence, Andrew McQuillin, Douglas Blackwood, Kevin McGhee, Andrew McIntosh, Alan W McLean, Walter J Muir, Benjamin S Pickard, René Breuer, Marcella Rietschel, Thomas G Schulze, Jana Strohmaier, Stephanie H Witt, Sarah E Bergen, Kim Chambert, Jennifer Moran, Vishwajit Nimgaonkar, Shaun Purcell, Pamela Sklar, Jordan Smoller, Christina Hultman, Mikael Landén, Paul Lichtenstein, Patrick Sullivan, Martin Schalling, Urban Osby, Lena Backlund, Louise Frisén, Sarah E Bergen, Shaun Purcell, Kim Chambert, Jennifer Moran, Niklas Langstrom, Pamela Sklar, Eli Stahl, Amanda Dobbyn, Laura Huckins, Stéphane Jamain, Marion Leboyer, Bruno Etain, Frank Bellivier, Bertram Müller‐Myhsok, Susanne Lucae, Markus Schwarz, Peter R Schofield, Nick Martin, Grant W Montgomery, Mark Lathrop, Sven Cichon, Thomas W Mühleisen, Franziska Degenhardt, Manuel Mattheisen, Johannes Schumacher, Wolfgang Maier, Michael Steffens, Thomas F Wienker, Peter Propping, Markus M Nöthen, Michael Bauer, Adam Wright, Philip B Mitchell, Martin Hautzinger, Andreas Reif, John R Kelsoe, Tiffany A Greenwood, Caroline M Nievergelt, Paul D Shilling, Nicholas J Schork, Erin N Smith, Cinnamon S Bloss, John I Nurnberger, Howard J Edenberg, Tatiana Foroud, Daniel L Koller, Elliot S Gershon, Chunyu Liu, Judith A Badner, William A Scheftner, William B Lawson, Evaristus A Nwulia, Maria Hipolito, William Coryell, John Rice, William Byerley, Francis J McMahon, Thomas G Schulze, Wade Berrettini, Falk W Lohoff, James B Potash, Peter P Zandi, Pamela B Mahon, Melvin G McInnis, Sebastian Zöllner, Peng Zhang, David W Craig, Szabolcs Szelinger, Gerome Breen, David St. Clair, Sian Caesar, Katherine Gordon‐Smith, Lisa Jones, Christine Fraser, Elaine K Green, Detelina Grozeva, Marian L Hamshere, Peter A Holmans, Ian R Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael C O'Donovan, Michael J Owen, Nick Craddock, David A Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H Young, I Nicol Ferrier, George Kirov, Vihra Milanova, George Kirov, Martin Alda, Pablo Cervantes, Cristiana Cruceanu, Guy A. Rouleau, Gustavo Turecki, Qingqin Li, Sara Paciga, Simon Xi, Ashley Winslow, Maria Grigoroiu‐Serbanescu, Roel Ophoff, Rolf Adolfsson, Annelie Nordin Adolfsson, Jurgen Del‐Favero, Carlos Pato, Joanna M Biernacka, and Mark A Frye CORtisol NETwork (CORNET) Consortium Bolton JL, Hayward CE, Direk N, Lewis JG, Hammond GL, Hill LA, Anderson AJ, Huffman J, Wilson JF, Campbell H, Rudan I, Wright A, Hastie N, Wild SH, Velders FP, Hofman A, Uitterlinden AG, Lati J, Raikonen K, Kajantie E, Widen E, Palotie A, Eriksson JG, Kaakinen M, Jarvelin M-R, Timpson NJ, Davey-Smith G, Ring SM, Evans DM, St Pourcain B, Tanaka T, Milaneschi Y, Bandinelli S, Ferrucci L, van der Harst P, Rosmalen JGM, Bakker SJL, Verweij N, Dullaart RPF, Mahajan A, Lindgren CM, Morris A, Lind L, Ingelsson E, Anderson LN, Pennell CE, Lye SJ, Matthews SG, Eriksson J, Mellstrom D, Ohlsson C, Price JF, Strachan MWJ, Reynolds RM, Tiemeier HW, Walker BR Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium Patrick Sullivan, Stephanie Ripke, Danielle Posthuma, Henning Tiemeier, André G Uitterlinden, Nese Direk, Saira Saeed Mirza, Albert Hofman, Susanne Lucae, Stefan Kloiber, Klaus Berger, Jürgen Wellmann, Bertram Müller‐Myhsok, Qingqin Li, Marcus Ising, Till Andlauer, Marcella Rietschel, Andreas Josef Forstner, Fabian Streit, Jana Strohmaier, Maren Lang, Josef Frank, Stefan Herms, Stephanie Witt, Jens Treutlein, Markus Nöthen, Sven Cichon, Franziska Degenhardt, Per Hoffmann, Thomas G. Schulze, Bernhard Baune, Udo Dannlowski, Tracy Air, Grant Sinnamon, Naomi Wray, Andrew McIntosh, Douglas Blackwood, Toni‐Kim Clarke, Donald MacIntyre, David Porteous, Caroline Hayward, Tonu Esko, Evelin Mihailov, Lili Milani, Andres Metspalu, Hans J Grabe, Henry Völzke, Alexander Teumer, Sandra Van der Auwera, Georg Homuth, Matthias Nauck, Cathryn Lewis, Gerome Breen, Margarita Rivera, Michael Gill, Nick Craddock, John P Rice, Michael Owen, Peter McGuffin, Henriette Buttenschøn, Ole Mors, Anders Børglum, Jakob Grove, Jesper Krogh, Enrico Domenici, Daniel Umbricht, Jorge A Quiroz, Carsten Horn, Enda Byrne, Baptiste Couvy‐Duchesne, Scott Gordon, Andrew C Heath, Anjali Henders, Ian Hickie, Pamela AF Madden, Nicholas Martin, Sarah Medland, Grant Montgomery, Dale Nyholt, Michele Pergadia, Divya Mehta, Martin Preisig, Enrique Castelao, Zoltán Kutalik, Steven Hamilton, Patrick McGrath, Katherine Tansey, Rudolf Uher, Glyn Lewis, Michael O'Donovan, Brenda WJH Penninx, Yuri Milaneschi, Wouter Peyrot, Johannes H Smit, Rick Jansen, Aartjan TF Beekman, Robert A Schoevers, Albert van Hemert, Gerard van Grootheest, Dorret Boomsma, Jouke‐ Jan Hottenga, Christel Middeldorp, Eco de Geus, Abdel Abdellaoui, Gonneke Willemsen, Erin Dunn, Roy Perlis, Jordan Smoller, Patrik Magnusson, Nancy Pedersen, Alexander Viktorin, Erik Pettersson, Thomas Werge, Thomas Folkmann Hansen, Sara Paciga, Hualin Xi, Ashley Winslow, Douglas Levinson, Myrna Weissman, James Potash, Jianxin Shi, and James Knowles METASTROKE consortium of the International Stroke Genetics Consortium. Rainer Malik, Matthew Traylor, Sara Pulit, Steve Bevan, Jemma Hopewell, Elizabeth Holliday, Wei Zhao, Patricia Abrantes, Philippe Amouyel, John Attia, Thomas Battey, Klaus Berger, Giorgio Boncoraglio, Ganesh Chauhan, Yu‐Ching Cheng, Wei‐Min Chen, Robert Clarke, Ioana Cotlarciuc, Stephanie Debette, Guido Falcone, Jose Ferro, Dale Gamble, Andreea Ilinca, Steven Kittner, Christina Kourkoulis, Robin Lemmens, Christopher Levi, Peter Lichtner, Arne Lindgren, James Meschia, Braxton Mitchell, Sofia Oliveira, Joana Pera, Alex Reiner, Peter Rothwell, Pankaj Sharma, Agnieszka Slowik, Cathie Sudlow, Turgut Tatlisumak, Vincent Thijs, Astrid Vicente, Daniel Woo, Sudha Seshadri, Danish Saleheen, Jonathan Rosand, Hugh Markus, Bradford Worrall, and Martin Dichgans. Obsessive Compulsive Disorder and Tourette Syndrome Working Group of the Psychiatric Genomics Consortium John Alexander, Paul Arnold, Harald Aschauer, Gil Atzmon, Cristina Barlassina, Cathy Barr, Csaba Barta, Robert Batterson, Laura Bellodi, Fortu Benarroch, Chester Berlin, Gabriel Berrio, O. Bienvenu, Donald Black, Michael Bloch, Rianne Blom, Julia Bohnenpoll, Helena Brentani, Lawrence W. Brown, Ruth Bruun,Randy Buckner, Cathy Budman, Christie Burton, Beatriz Camarena, Desmond Campbell, Carolina Cappi, Julio Cardona Silgado, Danielle Cath, Maria Cavallini, Keun‐Ah Cheon, Sylvain Chouinard, Barbara J. Coffey, David Conti, Edwin Cook, Giovanni Coppola, Vladimir Coric, Nancy Cox, Bernadette Cullen, Daniele Cusi, Sabrina Darrow, Lea Davis, Dieter Deforce, Richard Delorme, Damiaan Denys, Christel Depienne, Eske Derks, Andrea Dietrich, Yves Dion, Valsamma Eapen, Christopher Edlund, Karin Egberts, Lonneke Elzerman, Lauren Erdman, Patrick Evans, Peter Falkai, Thomas V. Fernandez, Martijn Figee, Nelson Freimer, Odette Fründt, Abby Fyer, Blanca Garcia‐Delgar, Helena Garrido, Daniel Geller, Gloria Gerber, Donald L. Gilbert, Hans Grabe, Marco Grados, Erica Greenberg, Benjamin Greenberg, Dorothy E. Grice, Varda Gross‐Tsur, Edna Grünblatt, Julie Hagstrøm, Gregory Hanna, Andreas Hartmann, Johannes Hebebrand, Tammy Hedderly, Gary A. Heiman, Sian Hemmings, Luis Herrera, Peter Heutink, Isobel Heyman, Matthew Hirschtritt, Pieter J. Hoekstra, Hyun Ju Hong, Ana Hounie, Alden Huang, Chaim Huyser, Laura Ibanez‐Gomez, Cornelia Illmann, Joseph Jankovic, Michael Jenike, Clare Keenan, James Kennedy, Judith Kidd, Kenneth Kidd, Young Key Kim, Young‐Shin Kim, Robert A. King, James Knowles, Yun‐Joo Koh, Anuar Konkashbaev, Anastasios Konstantinidis, Sodahm Kook, Samuel Kuperman, Roger Kurlan, Nuria Lanzagorta, Marion Leboyer, James Leckman, Phil Lee, Leonhard Lennertz, Bennett L. Leventhal, Bingbin Li, Christine Lochner, Thomas Lowe, Andrea G. Ludolph, Claudia Lührs da Silva, Sara Lupoli, Gholson Lyon, Fabio Macciardi, Marcos Madruga‐Garrido, Brion Maher, Wolfgang Maier, Irene Malaty, Paolo Manunta, Athanasios Maras, Maurizio Marconi, Carol A. Mathews, Manuel Mattheisen, James McCracken, Lauren McGrath, William McMahon, Sandra Mesa Restrepo, Euripedes Miguel, Pablo Mir, Rainald Moessner, Astrid Morer, Kirsten Müller‐Vahl, Alexander Münchau, Tara L. Murphy, Dennis Murphy, Allan Naarden, Peter Nagy, Benjamin Neale, Gerald Nestadt, Humberto Nicolini, Markus Noethen, Erika Nurmi, William Ochoa, Michael Okun, Lisa Osiecki, Andrew Pakstis, Peristera Paschou, Michele Pato, Carlos Pato, David Pauls, John Piacentini, Christopher Pittenger, Kerstin J. Plessen, Yehuda Pollak, Danielle Posthuma, Vasily Ramensky, Eliana Ramos, Scott Rauch, Tobias Renner, Victor Reus, Margaret Richter, Mark Riddle, Renata Rizzo, Mary Robertson, Veit Roessner, Josh Roffman, Maria Rosário, David Rosenberg, Guy Rouleau, Stephan Ruhrmann, Andres Ruiz‐Linares, Erika Salvi, Aline Sampaio, Jack Samuels, Paul Sandor, Jeremiah Scharf, Monika Schlögelhofer, Eun‐Young Shin, Yin Shugart, Harvey Singer, Jan Smit, Jordan Smoller, Dong‐Ho Song, Jungeun Song, Mara Stamenkovic, Matthew W. State, Dan J. Stein, S Stewart, Manfred Stuhrmann, Jae‐Hoon Sul, Urszula Szymanska, Zsanett Tarnok, Jay A. Tischfield, Fotis Tsetsos, Jennifer Tübing, Maurizio Turiel, Ana Valencia Duarte, Homero Vallada, Filip Van Nieuwerburgh, Jeremy Veenstra‐VanderWeele, Frank Visscher, Nienke Vulink, Michael Wagner, Susanne Walitza, John Walkup, Sina Wanderer, Ying Wang, Sarah Weatherall, Jens Wendland, Tomasz Wolanczyk, Aaron Wolf, Martin Woods, Yulia Worbe, Dongmei Yu, Ivette Zelaya, and Samuel H. Zinner. Schizophrenia Working Group of the Psychiatric Genomics Consortium Rolf Adolfsson, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Ole Andreassen, Silviu Bacanu, Martin Begemann, Richard Belliveau, Judit Bene, Sarah Bergen, Elizabeth Bevilacqua, Tim Bigdeli, Donald Black, Douglas Blackwood, Anders Børglum, Elvira Bramon, Richard Bruggeman, Nancy Buccola, Randy Buckner, Brendan Bulik‐Sullivan, Joseph Buxbaum, William Byerley, Wiepke Cahn, Guiqing Cai, Murray Cairns, Dominique Campion, Rita Cantor, Vaughan Carr, Noa Carrera, Stanley Catts, Kimberley Chambert, Raymond Chan, Eric Chen, Ronald Chen, Wei Cheng, Eric Cheung, Siow Chong, Sven Cichon, Robert Cloninger, David Cohen, Nadine Cohen, David Collier, Paul Cormican, Aiden Corvin, Nick Craddock, Benedicto Crespo‐Facorro, James Crowley, David Curtis, Mark Daly, Ariel Darvasi, Michael Davidson, Kenneth Davis, Franziska Degenhardt, Jurgen Del Favero, Lynn DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Enrico Domenici, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Hannelore Ehrenreich, Peter Eichhammer, Johan Eriksson, Valentina Escott‐Price, Tõnu Esko, Laurent Essioux, Ayman Fanous, Kai‐How Farh, Martilias Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson Freimer, Joseph Friedman, Menachem Fromer, Pablo Gejman, Giulio Genovese, Lyudmila Georgieva, Elliot Gershon, Ina Giegling, Michael Gill, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline Goldstein, Srihari Gopal, Jacob Gratten, Hugh Gurling, Lieuwe Haan, Christian Hammer, Marian Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette Hartmann, Frans Henskens, Stefan Herms, Joel Hirschhorn, Per Hoffmann, Andrea Hofman, Mads Hollegaard, Peter Holmans, David Hougaard, Hailiang Huang, Christina Hultman, Masashi Ikeda, Nakao Iwata, Assen Jablensky, Inge Joa, Erik Jönsson, Antonio Julià, Anna Kähler, René Kahn, Luba Kalaydjieva, Sena Karachanak‐Yankova, Juha Karjalainen, David Kavanagh, Matthew Keller, Brian Kelly, Kenneth Kendler, James Kennedy, Andrey Khrunin, Yunjung Kim, George Kirov, Janis Klovins, Jo Knight, James Knowles, Bettina Konte, Vaidutis Kucinskas, Zita Kucinskiene, Hana Kuzelova‐Ptackova, Claudine Laurent, Phil Lee, Hong Lee, Jimmy Lee Chee Keong, Sophie Legge, Todd Lencz, Bernard Lerer, Douglas Levinson, Miaoxin Li, Tao Li, Qingqin Li, Kung‐Yee Liang, Jeffrey Lieberman, Svetlana Limborska, Jianjun Liu, Jouko Lönnqvist, Carmel Loughland, Jan Lubinski, Milan Macek, Patrik Magnusson, Brion Maher, Wolfgang Maier, Anil Malhotra, Jacques Mallet, Sara Marsal, Manuel Mattheisen, Morten Mattingsdal, Robert McCarley, Steven McCarroll, Colm McDonald, Andrew McIntosh, Andrew McQuillin, Sandra Meier, Carin Meijer, Bela Melegh, Ingrid Melle, Raquelle Mesholam‐Gately, Andres Metspalu, Patricia Michie, Lili Milani, Vihra Milanova, Younes Mokrab, Jennifer Moran, Derek Morris, Ole Mors, Preben Mortensen, Bryan Mowry, Bertram Müller‐Myhsok, Kieran Murphy, Robin Murray, Inez Myin‐Germeys, Benjamin Neale, Mari Nelis, Igor Nenadic, Deborah Nertney, Gerald Nestadt, Kristin Nicodemus, Liene Nikitina‐Zake, Laura Nisenbaum, Annelie Nordin, Markus Nöthen, Eadbhard O'Callaghan, Michael O'Donovan, Colm O'Dushlaine, F O'Neill, Sang‐Yun Oh, Ann Olincy, Line Olsen, Roel Ophoff, Jim Os, Michael Owen, Sara Paciga, Aarno Palotie, Christos Pantelis, George Papadimitriou, Sergi Papiol, Elena Parkhomenko, Michele Pato, Carlos Pato, Tiina Paunio, Psychosis Endophenotypes International Consortium , Diana Perkins, Tune Pers, Tracey Petryshen, Olli Pietiläinen, Jonathan Pimm, Andrew Pocklington, Danielle Posthuma, John Powell, Alkes Price, Ann Pulver, Shaun Purcell, Digby Quested, Henrik Rasmussen, Abraham Reichenberg, Mark Reimers, Alexander Richards, Marcella Rietschel, Brien Riley, Stephan Ripke, Joshua Roffman, Panos Roussos, Douglas Ruderfer, Dan Rujescu, Veikko Salomaa, Alan Sanders, Ulrich Schall, Thomas Schulze, Sibylle Schwab, Edward Scolnick, Rodney Scott, Larry Seidman, Pak Sham, Jianxin Shi, Jeremy Silverman, Kang Sim, Pamela Sklar, Petr Slominsky, Jordan Smoller, Hon‐Cheong So, Erik Söderman, Chris Spencer, David Clair, Eli Stahl, Elisabeth Stogmann, Richard Straub, Eric Strengman, Jana Strohmaier, Scott Stroup, Mythily Subramaniam, Patrick Sullivan, Jaana Suvisaari, Dragan Svrakic, Jin Szatkiewicz, Srinivas Thirumalai, Draga Toncheva, Paul Tooney, Sarah Tosato, Peter Visscher, John Waddington, Dermot Walsh, James Walters, Dai Wang, Qiang Wang, Bradley Webb, Daniel Weinberger, Mark Weiser, Thomas Werge, Dieter Wildenauer, Nigel Williams, Stephanie Williams, Stephanie Witt, Aaron Wolen, Emily Wong, Brandon Wormley, Naomi Wray, Wellcome Trust Case‐Control Consortium 2 , Jing Wu, Hualin Xi, Clement Zai, Xuebin Zheng, and Fritz Zimp Yüklə 54,56 Kb. 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