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Paper Details

Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
273
2022
AMPA, GRIA3, GRIN2A, N-methyl-D-aspartate, NMDA, NMDA (N-methyl-D-aspartate) receptor subunit, URVs, associated genes, autism spectrum disorders, central nervous system neurons, dysfunction, epilepsy, exomes, genes, neurodevelopmental disorders, risk genes, schizophrenia, ultra-rare coding variants
Author NameAffiliation
Tarjinder SinghMassachusetts General Hospital
Tarjinder SinghBroad Institute of Harvard and MIT
Tarjinder SinghStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
David CurtisUCL Genetics Institute, University College London
David CurtisQueen Mary University London
Huda AkilMichigan Neuroscience Institute, University of Michigan ann arbor
Nicholas J BassUniversity College London
Gerome BreenInstitute of Psychiatry, King's College London
Gerome BreenInstitute of Psychiatry, King's College London
Jonas Bybjerg-GrauholmLundbeck Foundation Initiative for Integrative Psychiatric Research
Jonas Bybjerg-GrauholmCenter for Neonatal Screening, Statens Serum Institut
William ByerleyUniversity of California san francisco
Claire ChurchhouseMassachusetts General Hospital
Claire ChurchhouseStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Nick CraddockNational Centre for Mental Health, Cardiff University
Stephen V FaraoneSUNY Upstate Medical University
Stephen V FaraoneSUNY Upstate Medical University
Stacey GabrielBroad Institute of MIT and Harvard
Stacey GabrielBroad Institute of MIT and Harvard
Diane GageStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Andrea GannaMassachusetts General Hospital
Andrea GannaInstitute for Molecular Medicine Finland, University of Helsinki
Andrea GannaMassachusetts General Hospital
Andrea GannaInstitute for Molecular Medicine Finland, University of Helsinki
Giulio GenoveseStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
David C GlahnBoston Children's Hospital
Eija HämäläinenInstitute for Molecular Medicine Finland, University of Helsinki
David M HougaardLundbeck Foundation Initiative for Integrative Psychiatric Research
David M HougaardCenter for Neonatal Screening, Statens Serum Institut
Daniel P HowriganMassachusetts General Hospital
Daniel P HowriganStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Hailiang HuangMassachusetts General Hospital
Hailiang HuangStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Hyun Min KangDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
George KirovDivision of Psychological Medicine and Clinical Neurosciences, Cardiff University
James A KnowlesSUNY Downstate Medical Center
Francesco LescaiLundbeck Foundation Initiative for Integrative Psychiatric Research
Francesco LescaiAarhus University
Steven A McCarrollStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Steven A McCarrollHarvard Medical School
Lili MilaniInstitute of Genomics, University of Tartu
Derek W MorrisNational University of Ireland
Preben Bo MortensenAarhus University
Richard M MyersHudsonAlpha Institute for Biotechnology
Richard M MyersHudsonAlpha Institute for Biotechnology
Merete NordentoftLundbeck Foundation Initiative for Integrative Psychiatric Research
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