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(1 - 16 of 16)
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Body mass index and breast cancer survival: a Mendelian randomization analysis
PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1
Association analysis identifies 65 new breast cancer risk loci
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation
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
Genetic predisposition to ductal carcinoma in situ of the breast
Identification of Novel Genetic Markers of Breast Cancer Survival
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium