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(61 - 80 of 135)

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Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus
Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
RAD51B in Familial Breast Cancer
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
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Genetic predisposition to ductal carcinoma in situ of the breast
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

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