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(1 - 13 of 13)
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)
Genomic analysis and clinical management of adolescent cutaneous melanoma
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
The European Hematology Association Roadmap for European Hematology Research: a consensus document
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
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
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium