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Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
Body mass index and breast cancer survival: a Mendelian randomization analysis
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Identification of Novel Genetic Markers of Breast Cancer Survival
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
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
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
MicroRNA Related Polymorphisms and Breast Cancer Risk
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
Rare Mutations in RINT1 Predispose Carriers to Breast and Lynch Syndrome-Spectrum Cancers
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
Genome-wide association analysis identifies three new breast cancer susceptibility loci

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