Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Author:

Bassett Anne S.1,Lowther Chelsea1,Merico Daniele1,Costain Gregory1,Chow Eva W. C.1,van Amelsvoort Therese1,McDonald-McGinn Donna1,Gur Raquel E.1,Swillen Ann1,Van den Bree Marianne1,Murphy Kieran1,Gothelf Doron1,Bearden Carrie E.1,Eliez Stephan1,Kates Wendy1,Philip Nicole1,Sashi Vandana1,Campbell Linda1,Vorstman Jacob1,Cubells Joseph1,Repetto Gabriela M.1,Simon Tony1,Boot Erik1,Heung Tracy1,Evers Rens1,Vingerhoets Claudia1,van Duin Esther1,Zackai Elaine1,Vergaelen Elfi1,Devriendt Koen1,Vermeesch Joris R.1,Owen Michael1,Murphy Clodagh1,Michaelovosky Elena1,Kushan Leila1,Schneider Maude1,Fremont Wanda1,Busa Tiffany1,Hooper Stephen1,McCabe Kathryn1,Duijff Sasja1,Isaev Karin1,Pellecchia Giovanna1,Wei John1,Gazzellone Matthew J.1,Scherer Stephen W.1,Emanuel Beverly S.1,Guo Tingwei1,Morrow Bernice E.1,Marshall Christian R.1,

Affiliation:

1. From the Dalglish Family 22q Clinic, Department of Psychiatry, University Health Network, Toronto; the Department of Psychiatry and Toronto General Research Institute, University Health Network, Toronto; the Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto; the Department of Psychiatry, University of Toronto, Toronto; the Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto; the Centre for Applied Genomics and Program in...

Publisher

American Psychiatric Association Publishing

Subject

Psychiatry and Mental health

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