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Nature Genetics|April 20, 2010
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility geneAlfons Meindl, Heide Hellebrand, Constanze Wiek, et al.Nature Genetics|September 26, 2006
A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degenerationAnne E Hughes, Nick Orr, Hossein Esfandiary, et al.Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.Nature Genetics|October 31, 2006
Diversity of microRNAs in human and chimpanzee brainEugene Berezikov, Fritz Thuemmler, Linda W van Laake, et al.Nature Genetics|March 6, 2007
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndromeHiba Risheg, John M Graham, Robin D Clark, et al.Nature Genetics|March 6, 2007
Genetic basis of individual differences in the response to small-molecule drugs in yeastEthan O Perlstein, Douglas M Ruderfer, David C Roberts, et al.Nature Genetics|March 6, 2007
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genomeMichael Weber, Ines Hellmann, Michael B Stadler, et al.Nature Genetics|December 19, 2006
Integrative molecular concept modeling of prostate cancer progressionScott A Tomlins, Rohit Mehra, Daniel R Rhodes, et al.Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.Nature Genetics|June 8, 2007
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetesJohn A Todd, Neil M Walker, Jason D Cooper, et al.Pageof 744