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Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study
Genome-wide association study of germline variants and breast cancer-specific mortality
Shared heritability and functional enrichment across six solid cancers
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
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