Whole-exome sequencing identifies ten risk genes for schizophrenia implicated by rare protein-coding variants, a subset of which overlap with risk genes in other neurodevelopmental disorders.
We would like to thank the patients and families who participated in our studies during the past two decades, without whom our research and findings would not be possible. The research reported in this publication was supported by the National Institute of Mental Health and the National Human Genome Research Institute of the National Institutes of Health under award numbers U01 MH105641, U01 MH105578, U01 MH105666, U01 MH109539, R01 MH085548, R01 MH085521, R01 MH124851 and U54 HG003067.
Tarjinder Singh, Timothy Poterba, Claire Churchhouse, Laurent Francioli, Andrea Ganna, Henrike O. Heyne, Daniel P. Howrigan, Hailiang Huang, Konrad J. Karczewski, Duncan S. Palmer, F. Kyle Satterstrom, Aarno Palotie, Benjamin M. Neale & Mark J. DalyTarjinder Singh, Timothy Poterba, Sinéad B. Chapman, Claire Churchhouse, Caroline M. Cusick, Diane Gage, Giulio Genovese, Henrike O. Heyne, Daniel P. Howrigan, Hailiang Huang, Konrad J. Karczewski, Steven A.
Center for Neonatal Screening, Department for Congenital Disorders, Statens Serum Institut, Copenhagen, DenmarkDepartment of Psychiatry, University of California, San Francisco, San Francisco, CA, USAWei J. ChenDepartment of Psychiatry, Cambridge Health Alliance, Cambridge Hospital, Cambridge, MA, USASheila Dodge & Stacey B.
Tarjinder Singh, Laurent Francioli, Matthew Solomonson, Christine R. Stevens, Grace Tiao, Nicholas A. Watts, Aarno Palotie, Benjamin M. Neale & Mark J. DalyMontréal Heart Institute, Montreal, Quebec, CanadaInstitute for Molecular Medicine Finland, University of Helsinki, Helsinki, FinlandDepartment of Psychiatry, Boston Children’s Hospital, Boston, MA, USADepartment of Biomedicine and Center for Integrative Sequencing, Aarhus University, Aarhus, DenmarkJakob Grove & Anders D.
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