Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

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

Published:2017-11 Issue:11 Volume:174 Page:1054-1063
ISSN:0002-953X
Container-title:American Journal of Psychiatry
language:en
Short-container-title:AJP

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

Cited by 77 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Polygenic risk for triglyceride levels in the presence of a high impact rare variant;BMC Medical Genomics;2023-11-08

2. A review of 22q11.2 microdeletion syndrome: clinical and diagnostic perspective;The Journal of Medical Laboratory Science and Technology of South Africa;2023-05

3. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia;Molecular Psychiatry;2023-03-03

4. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

5. The contribution of copy number variants to psychiatric symptoms and cognitive ability;Molecular Psychiatry;2023-02-03