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Now showing items 1-12 of 12
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk
CSVS, a crowdsourcing database of the Spanish population genetic variability.
Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.
Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21.
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility
Genomic characterization of individuals presenting extreme phenotypes of high and low risk to develop tobacco-induced lung cancer
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk