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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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- Journal Article
- A1
- open access
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
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- Journal Article
- A1
- open access
Shared heritability and functional enrichment across six solid cancers
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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 12 new susceptibility loci for different histotypes of epithelial ovarian 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
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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
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- Journal Article
- A1
- open access
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers