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breast cancer
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BRCA1
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Hamann, U.
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Nevanlinna, H.
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Park, S.K.
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Andrulis, I.L.
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a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
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
Gene-environment interactions relevant to estrogen and risk of breast cancer
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Breast cancer risk genes
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
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
Two truncating variants in FANCC and breast cancer risk
Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
Association analysis identifies 65 new breast cancer risk loci
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
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