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PMID: 14962646 Published · ppublish English Journal Article

The common variants/multiple disease hypothesis of common complex genetic disorders.

Medical hypotheses ·Vol. 62 ·No. 2 ·2004-00-00 ·Pages 309-17

Becker KG

Abstract

Unlike simple rare Mendelian disorders, the genetic basis for common disorders is unclear. A general model of the genetics of common complex disorders is proposed which emphasizes the shared nature of common alleles in related common disorders, such as schizophrenia and bipolar disorder, Type II diabetes and obesity, and among autoimmune diseases. This model, the common variants/multiple disease hypothesis, emphasizes that many disease genes may not be disease specific. Common deleterious alleles, found at a relatively high frequency in the population may play a role in related clinical phenotypes in the context of different genetic backgrounds and under different environmental conditions.

MeSH Terms
Chromosome Mapping/methods Environment Gene Frequency/genetics Genetic Diseases, Inborn/genetics Genetic Predisposition to Disease/genetics Genetic Testing/methods Genetic Variation/genetics Humans Linkage Disequilibrium/genetics Models, Genetic Polymorphism, Single Nucleotide/genetics
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Becker Kevin G
Gene Expression and Genomics Unit, TRIAD Technology Center, National Institute on Aging, National Institutes on Health, Room 208, 333 Cassell Drive, Baltimore, MD 21224, USA. beckerk@grc.nia.nih.gov
Article Info
Journal
Medical hypotheses
Abbr.
Med Hypotheses
ISSN
0306-9877
Published
2004-00-00
Pages
309-17
Language
English
Region
United States
NLM ID
7505668
Subset
IM
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