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Nature Research, Nature Genetics, 9(40), p. 1056-1058, 2008

DOI: 10.1038/ng.209

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.

Journal article published in 2008 by Michael C. O'Donovan ORCID, Michael C. O’Donovan, Manuel A. R. Ferreira, Yan A. Meng, Ian R. Jones, Douglas M. Ruderfer ORCID, Lisa Jones, Jinbo Fan, George Kirov, Roy H. Perlis, Elaine K. Green, Jordan W. Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov and other authors.
This paper is available in a repository.
This paper is available in a repository.

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Data provided by SHERPA/RoMEO

Abstract

To identify susceptibility loci for bipolar disorder, we tested 1.8 million variants in 4,387 cases and 6,209 controls and identified a region of strong association (rs10994336, P = 9.1 10-9) in ANK3 (ankyrin G). We also found further support for the previously reported CACNA1C (alpha 1C subunit of the L-type voltage-gated calcium channel; combined P = 7.0 10-8, rs1006737). Our results suggest that ion channelopathies may be involved in the pathogenesis of bipolar disorder. ; PUBLISHED