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Breast cancer risk genes
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Overlapping genetic architecture between Parkinson disease and melanoma
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Germline TERT promoter mutations are rare in familial melanoma
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
POT1 loss-of-function variants predispose to familial melanoma
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers
Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk
Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor-Positive, Lower Grade Breast Cancer
7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium