Chromosomes 12 and 16 workshop

✍ Scribed by Detera-Wadleigh, Sevilla D.; Barden, N.; Craddock, N.; Ewald, H.; Foroud, T.; Kelsoe, J.; McQuillin, A.

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 24 KB
• Volume: 88
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/(sici)1096-8628(19990618)88:3<255::aid-ajmg8>3.0.co;2-v

✦ Synopsis

Recent linkage results independently derived from a large French Canadian pedigree and Danish kindreds coupled with supportive data from other studies provide compelling evidence for a bipolar disorder susceptibility locus on chromosome 12q23-q24. The idea is further strengthened by the finding that Darier's disease, which maps to this region, has been shown to cosegregate with affective disorder in a family. This linkage finding, however, was not supported in other independent genome scans. On chromosome 16, bipolar families from Denmark exhibited suggestive linkage with D16S510, on 16p13. Multipoint nonparametric analysis on the NIMH Genetics Initiative bipolar pedigrees yielded increased allele sharing that maximized ∼18 cM proximal to the latter locus. In contrast, evidence of linkage was not detected in other panels of bipolar families that were presented. At 16p13, a maximum multipoint lod score of 4 for a latent class-derived phenotype that has aspects of alcohol dependence was found in a genome scan of 105 families from the Collaborative Study of the Genetics of Alcoholism, identifying a potential vulnerability locus. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 88: 255-259, 1999.