Objective. To identify chromosomal regions containing genes involved in the susceptibility to primary Raynaud's phenomenon (RP). Methods. Six extended families with multiple individuals affected with primary RP (n β«Ψβ¬ 37) were examined for linkage in a 2-stage, whole-genome screen, using a total of
A genome-wide screen for nicotine dependence susceptibility loci
β Scribed by Gary E. Swan; Hyman Hops; Kirk C. Wilhelmsen; Christina N. Lessov-Schlaggar; Li S.-C. Cheng; Karen S. Hudmon; Christopher I. Amos; Heidi S. Feiler; Huijun Z. Ring; Judy A. Andrews; Elizabeth Tildesley; Neal Benowitz
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 125 KB
- Volume
- 141B
- Category
- Article
- ISSN
- 1552-4841
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Genomeβwide model free linkage analysis was conducted for nicotine dependence and tobacco use phenotypes in 607 members of 158 nuclear families consisting of at least two ever smokers (100 or more cigarettes smoked in lifetime). DNA from whole blood was genotyped for 739 autosomal microsatellite polymorphisms with an average interβmarker distance of 4.6 cM. A peak LOD score of 2.7 was observed on chromosome 6 for scores for the FagerstrΓΆm Test for Nicotine Dependence. Exploratory analyses were conducted to determine whether sequence variation at other loci affected other measures of dependence or tobacco use. Four additional loci with LOD scores of 2.7 or more were associated with alternative measures of nicotine dependence, one with current frequency of use, and one with smoking cessation. Several of the corresponding support intervals were near putative loci reported previously (on chromosomes 6, 7, and 8) while others appear to be novel (on chromosomes 5, 16, and 19). Β© 2006 WileyβLiss, Inc.
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