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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Physical activity, sedentary time and breast cancer risk
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
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
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Breast cancer risk genes
Two truncating variants in FANCC and breast cancer risk
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
Combined genetic and splicing analysis of BRCA1 c.[594-2A > C; 641A > G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
RAD51B in Familial Breast Cancer
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
FANCM c.5791C > T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1