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Now showing items 1-8 of 8
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility
Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size
Understanding cardiovascular disease: a journey through the genome (and what we found there)