A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Edward I. Ginns, Jurg Ott, Janice A. Egeland, Cleona R. Allen, Cathy S.J. Fann, David L. Pauls, Jean Weissenbach, John P. Carulli, Kathleen M. Falls, Tim P. Keith, Steven M. Paul

Research output: Contribution to journalArticlepeer-review

153 Scopus citations


The most characteristic features of bipolar affective disorder (manic- depressive illness) are episodes of mania (bipolar I, BPI) or hypomania (bipolar II, BPII) interspersed with periods of depression. Manic-depressive illness afflicts about one percent of the population, and if untreated, is associated with an approximately 20% risk of suicide. Twin, family and adoption studies provide compelling evidence for a partial genetic aetiology, but the mode(s) of inheritance has not been identified. Nonetheless, the majority of genetic linkage studies have assumed classical mendelian inheritance attributable to a single major gene. Although segregation analyses have yielded inconsistent results (with most studies rejecting a single locus inheritance model), the best single gene model is dominant inheritance if only BPI is considered. Reported linkages of bipolar affective disorder on chromosomes 11, 18, 21 and X have been difficult to substantiate, and additional studies are required for replication or exclusion of these regions. We now present the results of our genome-wide linkage analyses that provide evidence that regions on chromosomes 6, 13 and 15 harbour susceptibility loci for bipolar affective disorder, suggesting that bipolar affective disorder in the Old Order Amish is inherited as a complex trait.

Original languageEnglish (US)
Pages (from-to)431-435
Number of pages5
JournalNature genetics
Issue number4
StatePublished - Apr 1996

ASJC Scopus subject areas

  • Genetics


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