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(1 - 20 of 20)
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
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
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
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
FANCM c.5791C > T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk