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(61 - 80 of 97)

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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
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
SNP-SNP interaction analysis of NF-kappa B signaling pathway on breast cancer survival
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
Identification of Novel Genetic Markers of Breast Cancer Survival
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
New genetic loci link adipose and insulin biology to body fat distribution
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
New genetic loci link adipose and insulin biology to body fat distribution

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