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a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
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
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
Breast cancer risk genes
Contribution of mRNA splicing to mismatch repair gene sequence variant interpretation
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
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
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Shared heritability and functional enrichment across six solid cancers
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2
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