Genome-wide investigation of rare structural variants identifies VIPR2 as a new candidate gene for schizophrenia.

Abstract:

:Research has shown that structural variation in the human genome, including rare copy number variations (CNVs), contributes to genetic susceptibility to psychiatric diseases, such as schizophrenia, a devastating complex disorder with a high genetic load. The study by Vacic et al. applied a genome-wide approach to detect novel, rare and highly penetrant CNVs. Detailed analysis of microduplications at 7q36.3 revealed that the neuropeptide receptor gene VIPR2 confers a significant risk for schizophrenia. This suggests that altered vasoactive intestinal signaling contributes to the genetic etiology of this disorder. This article recapitulates the findings of this study within the context of current knowledge of CNVs in the field of psychiatric disease.

journal_name

Expert Rev Neurother

authors

Nieratschker V,Meyer-Lindenberg A,Witt SH

doi

10.1586/ern.11.84

subject

Has Abstract

pub_date

2011-07-01 00:00:00

pages

937-41

issue

7

eissn

1473-7175

issn

1744-8360

journal_volume

11

pub_type

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