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Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide association study of germline variants and breast cancer-specific mortality
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Association analysis identifies 65 new breast cancer risk loci
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
Identification of Novel Genetic Markers of Breast Cancer Survival
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