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PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
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
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
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)
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Shared heritability and functional enrichment across six solid cancers
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension