The usefulness of different density SNP maps for disease association studies of common variants
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/12/23/3145/17240600/ddg337.pdf
Reference19 articles.
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2. Botstein, D. and Risch, N. (2003) Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat. Genet., 33, 228–237.
3. Lohmueller, K.E., Pearce, C.L., Pike, M., Lander, E.S. and Hirschhorn, J.N. (2003) Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat. Genet., 33, 177–182.
4. Kruglyak, L. and Nickerson, D.A. (2001) Variation is the spice of life. Nat. Genet., 27, 234–236.
5. Carlson, C.S., Eberle, M.A., Rieder, M.J., Smith, J.D., Kruglyak, L. and Nickerson, D.A. (2003) Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans. Nat. Genet., 33, 518–521.
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