An investigation of candidate regions for association with bipolar disorder

NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium, NIMH Genetics Initiative Bipolar Disorder Consortium

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

We performed a case-control study of 1,000 cases and 1,028 controls on 1,509 markers, 1,139 of which were located in a 8Mb region on chromosome 6 (105-113 Mb). This region has shown evidence of involvement in bipolar disorder (BP) in a number of other studies. We find association between BP and two SNPs in the gene LACE1. SNP rs9486880 and rs11153113 (both have P-values of 2×10-5). Both P-values are in the top 5% of the distribution derived from null simulations (P=0.02 and 0.01, respectively). LACE is a good candidate for BP; it is an ATPase. We genotyped 173 other markers in 17 other positional and/or functional loci but found no further evidence of association with BP.

Original languageEnglish (US)
Pages (from-to)1292-1297
Number of pages6
JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume153
Issue number7
DOIs
StatePublished - Oct 1 2010

Funding

Keywords

  • Association
  • Bipolar disorder
  • Genetics

ASJC Scopus subject areas

  • Genetics(clinical)
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

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