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- Journal Article
- A1
- open access
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
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- Journal Article
- A1
- open access
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
- open access
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative 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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- Journal Article
- A1
- open access
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer