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Meta-analysis of genetic association studies on bipolar disorder.


ABSTRACT: Numerous candidate gene association studies of bipolar disorder (BP) have been carried out, but the results have been inconsistent. Individual studies are typically underpowered to detect associations with genes of small effect sizes. We conducted a meta-analysis of published candidate gene studies to evaluate the cumulative evidence. We systematically searched for all published candidate gene association studies of BP. We then carried out a random-effects meta-analysis on all polymorphisms that were reported on by three or more case-control studies. The results from meta-analyses of these genes were compared with the findings from a recent mega-analysis of eleven genome-wide association studies (GWAS) in BP performed by the Psychiatric GWAS Consortium (PGC). A total of 487 articles were included in our review. Among these, 33 polymorphisms in 18 genes were reported on by three or more case-control studies and included in the random-effects meta-analysis. Polymorphisms in BDNF, DRD4, DAOA, and TPH1, were found to be nominally significant with a P-value?

SUBMITTER: Seifuddin F 

PROVIDER: S-EPMC3582382 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

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Meta-analysis of genetic association studies on bipolar disorder.

Seifuddin Fayaz F   Mahon Pamela Belmonte PB   Judy Jennifer J   Pirooznia Mehdi M   Jancic Dubravka D   Taylor Jacob J   Goes Fernando S FS   Potash James B JB   Zandi Peter P PP  

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 20120509 5


Numerous candidate gene association studies of bipolar disorder (BP) have been carried out, but the results have been inconsistent. Individual studies are typically underpowered to detect associations with genes of small effect sizes. We conducted a meta-analysis of published candidate gene studies to evaluate the cumulative evidence. We systematically searched for all published candidate gene association studies of BP. We then carried out a random-effects meta-analysis on all polymorphisms that  ...[more]

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