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(1 - 18 of 18)
Association analysis identifies 65 new breast cancer risk loci
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for 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
2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
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
Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers
Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
19p13.1 Is a Triple-Negative-Specific Breast Cancer Susceptibility Locus
Genome-wide association analysis identifies three new breast cancer susceptibility loci
Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the breast cancer association consortium studies