Schizophrenia genetics: advancing on two fronts.

Abstract:

:Recent studies have supported the hypothesis that the high heritability of schizophrenia reflects a combination of relatively common alleles of small effect and some rare alleles with relatively large effects. Genome-wide association studies have identified at least one common allele of small effect at ZNF804a, which encodes a putative zinc finger binding protein, as well as possible roles for other loci. The genome-wide studies of at least one class of relatively uncommon variant, submicroscopic chromosomal abnormalities often referred to as copy number variations (CNVs), suggest that these confer high risk of schizophrenia. There is evidence both for an increased burden of CNVs in schizophrenia and that risk is conferred by specific large deletions at 1q21.1 and at 15q13.2 and by deletions of NRXN1 which encodes the synaptic scaffolding protein neurexin 1.

journal_name

Curr Opin Genet Dev

authors

Owen MJ,Williams HJ,O'Donovan MC

doi

10.1016/j.gde.2009.02.008

subject

Has Abstract

pub_date

2009-06-01 00:00:00

pages

266-70

issue

3

eissn

0959-437X

issn

1879-0380

pii

S0959-437X(09)00049-5

journal_volume

19

pub_type

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