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Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.Nature Genetics|March 14, 2023
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populationsDongjing Liu, Dara Meyer, Brian Fennessy, et al.Nature Genetics|August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingAlejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.Pageof 4