Deletion of Rapgef6, a candidate schizophrenia susceptibility gene, disrupts amygdala function in mice-Reference-Cited by-同舟云学术

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Deletion of Rapgef6, a candidate schizophrenia susceptibility gene, disrupts amygdala function in mice

Published:2015-06 Issue:6 Volume:5 Page:e577-e577
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Levy R J,Kvajo M,Li Y,Tsvetkov E,Dong W,Yoshikawa Y,Kataoka T,Bolshakov V Y,Karayiorgou M,Gogos J A

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

Link

http://www.nature.com/articles/tp201575.pdf

Reference87 articles.

1. Cross-Disorder Group of the Psychiatric Genomics C. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet 2013; 381: 1371–1379.

2. Xu B, Ionita-Laza I, Roos JL, Boone B, Woodrick S, Sun Y et al. De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia. Nat Genet 2012; 44: 1365–1369.

3. Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M . Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet 2008; 40: 880–885.

4. Xu B, Woodroffe A, Rodriguez-Murillo L, Roos JL, van Rensburg EJ, Abecasis GR et al. Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans. Proc Natl Acad Sci USA 2009; 106: 16746–16751.

5. Bennett RL, Karayiorgou M, Sobin CA, Norwood TH, Kay MA . Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1. Am J Hum Genet 1997; 61: 1450–1454.

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