Literature DB >> 14962646

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

Kevin G Becker1.   

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.

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Year:  2004        PMID: 14962646     DOI: 10.1016/S0306-9877(03)00332-3

Source DB:  PubMed          Journal:  Med Hypotheses        ISSN: 0306-9877            Impact factor:   1.538


  39 in total

1.  Meta-analysis of TYK2 gene polymorphisms association with susceptibility to autoimmune and inflammatory diseases.

Authors:  Jin-Hui Tao; Yan-Feng Zou; Xiao-Liang Feng; Jing Li; Fang Wang; Fan-Ming Pan; Dong-Qing Ye
Journal:  Mol Biol Rep       Date:  2010-12-08       Impact factor: 2.316

Review 2.  Detecting shared pathogenesis from the shared genetics of immune-related diseases.

Authors:  Alexandra Zhernakova; Cleo C van Diemen; Cisca Wijmenga
Journal:  Nat Rev Genet       Date:  2009-01       Impact factor: 53.242

3.  Effects of common atopy-associated amino acid substitutions in the IL-4 receptor alpha chain on IL-4 induced phenotypes.

Authors:  Izolda Franjkovic; Andre Gessner; Inke König; Karin Kissel; Anette Bohnert; Anne Hartung; Astrid Ohly; Andreas Ziegler; Holger Hackstein; Gregor Bein
Journal:  Immunogenetics       Date:  2005-01-27       Impact factor: 2.846

4.  Cigarette smoking associates inversely with a cluster of two autoimmune diseases: ulcerative colitis and pemphigus.

Authors:  Khalaf Kridin; Hadas Zamir; Arnon D Cohen
Journal:  Immunol Res       Date:  2018-08       Impact factor: 2.829

5.  Rasmussen encephalitis and comorbid autoimmune diseases: A window into disease mechanism?

Authors:  Dina Amrom; Demet Kinay; Yvonne Hart; Samuel F Berkovic; Ken Laxer; Frederick Andermann; Eva Andermann; Amit Bar-Or
Journal:  Neurology       Date:  2014-08-20       Impact factor: 9.910

6.  Associations between the FAS -670 A/G and -1,377 G/A polymorphisms and susceptibility to autoimmune rheumatic diseases: a meta-analysis.

Authors:  Young Ho Lee; Sang-Cheol Bae; Sung Jae Choi; Jong Dae Ji; Gwan Gyu Song
Journal:  Mol Biol Rep       Date:  2012-10-05       Impact factor: 2.316

Review 7.  Morphomechanic phenotypic variability of sarcomeric cardiomyopathies: A multifactorial polygenic perspective.

Authors:  Ares Pasipoularides
Journal:  J Mol Cell Cardiol       Date:  2018-11-10       Impact factor: 5.000

8.  Common genetic determinants of uveitis shared with other autoimmune disorders.

Authors:  Mary J Mattapallil; Azize Sahin; Phyllis B Silver; Shu-Hui Sun; Chi-Chao Chan; Elaine F Remmers; J Fielding Hejtmancik; Rachel R Caspi
Journal:  J Immunol       Date:  2008-05-15       Impact factor: 5.422

Review 9.  The contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitis.

Authors:  Lisa C Willcocks; Paul A Lyons; Andrew J Rees; Kenneth G C Smith
Journal:  Arthritis Res Ther       Date:  2010-02-15       Impact factor: 5.156

10.  Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information.

Authors:  Yonqing Zhang; Supriyo De; John R Garner; Kirstin Smith; S Alex Wang; Kevin G Becker
Journal:  BMC Med Genomics       Date:  2010-01-21       Impact factor: 3.063

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