Finding the missing heritability of complex diseases-Reference-Cited by-同舟云学术

Finding the missing heritability of complex diseases

Published:2009-10 Issue:7265 Volume:461 Page:747-753
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Manolio Teri A.,Collins Francis S.,Cox Nancy J.,Goldstein David B.,Hindorff Lucia A.,Hunter David J.,McCarthy Mark I.,Ramos Erin M.,Cardon Lon R.,Chakravarti Aravinda,Cho Judy H.,Guttmacher Alan E.,Kong Augustine,Kruglyak Leonid,Mardis Elaine,Rotimi Charles N.,Slatkin Montgomery,Valle David,Whittemore Alice S.,Boehnke Michael,Clark Andrew G.,Eichler Evan E.,Gibson Greg,Haines Jonathan L.,Mackay Trudy F. C.,McCarroll Steven A.,Visscher Peter M.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature08494.pdf

Reference84 articles.

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3. Hindorff, L. A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. 106, 9362–9367 (2009)Comprehensive analysis of genomic annotations for disease-associated SNPs defined by GWAS, showing great majority of associated loci in intronic or intergenic regions of unknown function.

4. Hindorff, L. A., Junkins, H. A., Mehta, J. P. & Manolio, T. A. A catalog of published genome-wide association studies. Available at 〈 http://www.genome.gov/26525384 〉 (accessed, 18 September 2009)

5. Hirschhorn, J. N., Lohmueller, K., Byrne, E. & Hirschhorn, K. A comprehensive review of genetic association studies. Genet. Med. 4, 45–61 (2002)

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