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Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21.
Vitamin D metabolic pathway genes and pancreatic cancer risk.