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  • (-) = Chenevix-Trench, G.

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(1 - 20 of 133)

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PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
The impact of coding germline variants on contralateral breast cancer risk and survival
FANCM missense variants and breast cancer riskn
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Pathology of tumors associated with pathogenic germline variants in 9 breast cancer susceptibility genes
Rare germline copy number variants (CNVs) and breast cancer risk
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Genetic insights into biological mechanisms governing human ovarian ageing
Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores
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
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Breast cancer risk genes
CYP3A7*1C allele
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

Pages