Literature DB >> 20403315

Genetic heterogeneity in human disease.

Jon McClellan1, Mary-Claire King.   

Abstract

Strong evidence suggests that rare mutations of severe effect are responsible for a substantial portion of complex human disease. Evolutionary forces generate vast genetic heterogeneity in human illness by introducing many new variants in each generation. Current sequencing technologies offer the possibility of finding rare disease-causing mutations and the genes that harbor them. Copyright 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20403315     DOI: 10.1016/j.cell.2010.03.032

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  458 in total

Review 1.  Five years of GWAS discovery.

Authors:  Peter M Visscher; Matthew A Brown; Mark I McCarthy; Jian Yang
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

2.  Genomics of human health and aging.

Authors:  Alexander M Kulminski; Irina Culminskaya
Journal:  Age (Dordr)       Date:  2011-12-16

3.  Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis.

Authors:  Elizabeth E Marchani; Ellen M Wijsman
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

4.  The mystery of missing heritability: Genetic interactions create phantom heritability.

Authors:  Or Zuk; Eliana Hechter; Shamil R Sunyaev; Eric S Lander
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-05       Impact factor: 11.205

5.  Candidate pathway based analysis for cleft lip with or without cleft palate.

Authors:  Tian-Xiao Zhang; Terri H Beaty; Ingo Ruczinski
Journal:  Stat Appl Genet Mol Biol       Date:  2012-01-06

6.  Evolutionary meta-analysis of association studies reveals ancient constraints affecting disease marker discovery.

Authors:  Joel T Dudley; Rong Chen; Maxwell Sanderford; Atul J Butte; Sudhir Kumar
Journal:  Mol Biol Evol       Date:  2012-03-01       Impact factor: 16.240

Review 7.  CNVs: harbingers of a rare variant revolution in psychiatric genetics.

Authors:  Dheeraj Malhotra; Jonathan Sebat
Journal:  Cell       Date:  2012-03-16       Impact factor: 41.582

Review 8.  Multiple sclerosis.

Authors:  Alyssa Nylander; David A Hafler
Journal:  J Clin Invest       Date:  2012-04-02       Impact factor: 14.808

Review 9.  Network analysis of GWAS data.

Authors:  Mark D M Leiserson; Jonathan V Eldridge; Sohini Ramachandran; Benjamin J Raphael
Journal:  Curr Opin Genet Dev       Date:  2013-11-26       Impact factor: 5.578

Review 10.  Electrophysiological Endophenotypes for Schizophrenia.

Authors:  Emily M Owens; Peter Bachman; David C Glahn; Carrie E Bearden
Journal:  Harv Rev Psychiatry       Date:  2016 Mar-Apr       Impact factor: 3.732

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.