Authors
Danielle M Dick, Tatiana Foroud, Leah Flury, Elizabeth S Bowman, Marvin J Miller, N Leela Rau, P Ryan Moe, Nalini Samavedy, Rif El-Mallakh, Husseini Manji, Debra A Glitz, Eric T Meyer, Carrie Smiley, Rhoda Hahn, Clifford Widmark, Rebecca McKinney, Laura Sutton
Publication date
2003/7/31
Journal
The American Journal of Human Genetics
Volume
73
Issue
1
Pages
107-114
Publisher
Cell Press
Description
We conducted genomewide linkage analyses on 1,152 individuals from 250 families segregating for bipolar disorder and related affective illnesses. These pedigrees were ascertained at 10 sites in the United States, through a proband with bipolar I affective disorder and a sibling with bipolar I or schizoaffective disorder, bipolar type. Uniform methods of ascertainment and assessment were used at all sites. A 9-cM screen was performed by use of 391 markers, with an average heterozygosity of 0.76. Multipoint, nonparametric linkage analyses were conducted in affected relative pairs. Additionally, simulation analyses were performed to determine genomewide significance levels for this study. Three hierarchical models of affection were analyzed. Significant evidence for linkage (genomewide P<.05) was found on chromosome 17q, with a peak maximum LOD score of 3.63, at the marker D17S928, and on …
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