Guidelines for association studies in Human Molecular Genetics
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/14/17/2481/1522817/ddi251.pdf
Reference18 articles.
1. Freimer, N. and Sabatti, C. (2004) The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology (review). Nat. Genet., 36(10), 1045–1051.
2. Sabatti, C., Service, S. and Freimer, N. (2003) False discovery rate in linkage and association genome screens for complex disorders. Genetics, 164, 829–833.
3. Storey, J.D. and Tibshirani, R. (2003) Statistical significance for genomewide studies. Proc. Natl Acad. Sci. USA, 100, 9440–9445.
4. Wacholder, S., Chanock, S., Garcia-Closas, M., El Ghormli, L. and Rothman, N. (2004) Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. J. Natl Cancer Inst., 96, 434–442.
5. McPeek, M.S. and Strahs, A. (1999) Assessment of linkage disequilibrium by the decay of haplotype sharing, with application to fine-scale genetic mapping. Am. J. Hum. Genet., 65(3), 858–875.
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