Understanding rare and common diseases in the context of human evolution
Author:
Funder
Centre National de la Recherche Scientifique
Institut Pasteur
European Research Council
Publisher
Springer Science and Business Media LLC
Link
http://link.springer.com/content/pdf/10.1186/s13059-016-1093-y.pdf
Reference206 articles.
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3. Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. Finding the missing heritability of complex diseases. Nature. 2009;461:747–53.
4. McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JP, et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet. 2008;9:356–69.
5. Reich DE, Lander ES. On the allelic spectrum of human disease. Trends Genet. 2001;17:502–10.
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