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

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

Journal
American Journal of Psychiatry
ISSN
0002-953X
1535-7228
Date Issued
2017
Author(s)
Anne S. Bassett
Chelsea Lowther
Daniele Merico
Gregory Costain
Eva W. C. Chow
Therese van Amelsvoort
Donna McDonald-McGinn
Raquel E. Gur
Ann Swillen
Marianne Van den Bree
Kieran Murphy
Doron Gothelf
Carrie E. Bearden
Stephan Eliez
Wendy Kates
Nicole Philip
Vandana Sashi
Linda Campbell
Jacob Vorstman
Joseph Cubells
Gabriela M. Repetto  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Tony Simon
Erik Boot
Tracy Heung
Rens Evers
Claudia Vingerhoets
Esther van Duin
Elaine Zackai
Elfi Vergaelen
Koen Devriendt
Joris R. Vermeesch
Michael Owen
Clodagh Murphy
Elena Michaelovosky
Leila Kushan
Maude Schneider
Wanda Fremont
Tiffany Busa
Stephen Hooper
Kathryn McCabe
Sasja Duijff
Karin Isaev
Giovanna Pellecchia
John Wei
Matthew J. Gazzellone
Stephen W. Scherer
Beverly S. Emanuel
Tingwei Guo
Bernice E. Morrow
Christian R. Marshall
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85032969720
WoS ID
WOS:000414240700007
DOI
10.1176/appi.ajp.2017.16121417
URL
https://investigadores.udd.cl/handle/123456789/9321
URL Institutional Repository
http://hdl.handle.net/11447/1869
Subjects
chromosomal microarray

; 

risk

; 

variants

; 

disorders

; 

microduplications

; 

integration

; 

mechanisms

; 

childhood

; 

mutations

; 

burden
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