LINKAGE ANALYSIS OF 57 MICROSATELLITE LOCI TO BIPOLAR DISORDER

被引:44
作者
GEJMAN, PV
MARTINEZ, M
CAO, QH
FRIEDMAN, E
BERRETTINI, WH
GOLDIN, LR
KOROULAKIS, P
AMES, C
LERMAN, MA
GERSHON, ES
机构
[1] INSERM, F-75005 PARIS, FRANCE
[2] KAROLINSKA HOSP, DEPT CLIN GENET, S-10401 STOCKHOLM 60, SWEDEN
[3] THOMAS JEFFERSON UNIV, JEFFERSON MED COLL, DEPT PSYCHIAT & HUMAN BEHAV, PHILADELPHIA, PA 19107 USA
关键词
MAPPING; BIPOLAR ILLNESS; MICROSATELLITES; GENETIC LINKAGE SIMULATIONS; GNAS1; HUMAN X-LINKED GABA-A RECEPTOR ALPHA-3-SUBUNIT GENE;
D O I
10.1038/npp.1993.40
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The authors' goal was to screen for genetic linkage with highly informative deoxyribonucleic acid (DNA) microsatellite markers on a series of moderately sized North American bipolar disorder (BP) pedigrees. These BP pedigrees were genotyped with 57 short tandem-repeat polymorphic systems (microsatellites) that were enzymatically amplified from genomic DNA. We did not find significant evidence for genetic linkage. We und isolated LOD scores greater than 2 on chromosome 1 at two loci in individual pedigrees. Simulation studies for multiple analyses under the assumptions of linkage and nonlinkage were performed. The simulations show that LOD scores greater than 2 could be expected even when linkage is absent. Significance levels need to be considered carefully in systematic linkage studies.
引用
收藏
页码:31 / 40
页数:10
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