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Curr Opin Psychiatry DOI:10.1097/YCO.0b013e32835035dd

Genome-wide association studies of schizophrenia: does bigger lead to better results?

Publication TypeJournal Article
Year of Publication2012
AuthorsBergen, SE, Petryshen, TL
JournalCurr Opin Psychiatry
Volume25
Issue2
Pages76-82
Date Published2012 Mar
ISSN1473-6578
KeywordsGenetic Markers, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Sample Size, Schizophrenia
Abstract

PURPOSE OF REVIEW: Numerous genome-wide association studies (GWAS) of schizophrenia have been published in the past 6 years, with a number of key reports published in the last year. The studies have evolved in scale from small individual samples to large collaborative endeavors. This review aims to critically assess whether the results have improved as the sample size and scale of genetic association studies have grown.

RECENT FINDINGS: Genomic genotyping and increasing sample sizes for schizophrenia association studies have led to parallel increases in the number of risk genes discovered with high statistical confidence. Nearly 20 genes or loci have surpassed the genome-wide significance threshold (P = 5 × 10) in a single study, and several have been replicated in more than one GWAS.

SUMMARY: Identifying the genetic underpinnings of complex diseases offers insight into the etiological mechanisms leading to manifestation of the disease. New and more effective treatments for schizophrenia are desperately needed, and the ability to target the relevant biological processes grows with our understanding of the genes involved. As the size of GWAS samples has increased, more genes have been identified with high confidence that have begun to provide insight into the etiological and pathophysiological foundations of this disorder.

URLhttp://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0951-7367&volume=25&issue=2&spage=76
DOI10.1097/YCO.0b013e32835035dd
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/22277805?dopt=Abstract

Alternate JournalCurr Opin Psychiatry
PubMed ID22277805
PubMed Central IDPMC3771358
Grant ListP50 MH080272 / MH / NIMH NIH HHS / United States
MH080272 / MH / NIMH NIH HHS / United States