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PMID: 1632891 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A systematic search for a bipolar predisposing locus on chromosome 5.

Detera-Wadleigh SD, Berrettini WH, Goldin LR, Martinez M, Hsieh WT, Hoehe MR, Encio IJ, Coffman D, Rollins DY, Muniec D

Abstract

Chromosome 5 markers spanning the pter to the qter were used to examine linkage to bipolar illness in 14 pedigrees. Twenty-four loci were examined in 237 individuals, of whom 69 were either bipolars or schizoaffectives. Marker genotypes were determined for each individual and lod scores were calculated under a dominant disease model with a maximum penetrance of 85%, a disease gene frequency of 0.015, a variable age of onset, and a phenocopy rate of 0.001. Under the assumption that bipolar illness is genetically homogeneous, the total lod scores from all pedigrees with each marker were uniformly lower than -2.0, suggesting the absence of linkage to disease at any of these loci. Multipoint analysis allowed exclusion of intervals between markers. When lod scores were calculated allowing for heterogeneity, no subset of linked families was found. These results indicate that in our pedigree series almost the entire mapped region of chromosome 5 can be excluded for linkage to bipolar illness.

MeSH Terms
Bipolar Disorder/diagnosis,genetics Chromosomes, Human, Pair 5 Family Female Genetic Linkage Genetic Markers Genome Genotype Humans Male Nucleic Acid Hybridization
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Detera-Wadleigh S D
Clinical Neurogenetics Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Berrettini W H
Goldin L R
Martinez M
Hsieh W T
Hoehe M R
Encio I J
Coffman D
Rollins D Y
Muniec D
Article Info
Journal
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Abbr.
Neuropsychopharmacology
ISSN
0893-133X
Published
1992-06-00
Pages
219-29
Language
English
Region
England
NLM ID
8904907
Subset
IM
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