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Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
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- Journal Article
- A1
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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
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- Journal Article
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Shared heritability and functional enrichment across six solid cancers
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- Journal Article
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
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BRCA2 hypomorphic missense variants confer moderate risks of breast cancer
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- Journal Article
- A1
- open access
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
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BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers