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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
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)
Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes
Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148
Germline TERT promoter mutations are rare in familial melanoma
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
Identification of a melanoma susceptibility locus and somatic mutation in TET2
POT1 loss-of-function variants predispose to familial melanoma
A variant in FTO shows association with melanoma risk not due to BMI
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
Genome-wide association study identifies three new melanoma susceptibility loci