Genome partitioning of genetic variation for complex traits using common SNPs-Reference-Cited by-同舟云学术

Genome partitioning of genetic variation for complex traits using common SNPs

Published:2011-05-08 Issue:6 Volume:43 Page:519-525
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Yang Jian,Manolio Teri A,Pasquale Louis R,Boerwinkle Eric,Caporaso Neil,Cunningham Julie M,de Andrade Mariza,Feenstra Bjarke,Feingold Eleanor,Hayes M Geoffrey,Hill William G,Landi Maria Teresa,Alonso Alvaro,Lettre Guillaume,Lin Peng,Ling Hua,Lowe William,Mathias Rasika A,Melbye Mads,Pugh Elizabeth,Cornelis Marilyn C,Weir Bruce S,Goddard Michael E,Visscher Peter M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.823.pdf

Reference43 articles.

1. Hindorff, L.A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl. Acad. Sci. USA 106, 9362–9367 (2009).

2. Manolio, T.A. et al. Finding the missing heritability of complex diseases. Nature 461, 747–753 (2009).

3. Manolio, T.A. Genomewide association studies and assessment of the risk of disease. N. Engl. J. Med. 363, 166–176 (2010).

4. Yang, J. et al. Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565–569 (2010).

5. Visscher, P.M. et al. Genome partitioning of genetic variation for height from 11,214 sibling pairs. Am. J. Hum. Genet. 81, 1104–1110 (2007).

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