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Genome-wide Association Study identifies ALDH7A1 as a Novel Susceptibility Gene for Osteoporosis
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
Genetic variability in the MTHFR gene and colorectal cancer risk using the colorectal cancer family registry
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene
Common variants at 19p13 are associated with susceptibility to ovarian cancer
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
Germline mutations in breast and ovarian cancer pedigrees established RAD51C as a human cancer susceptibility gene