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Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families
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
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Development and Validation of a Melanoma Risk Score Based on Pooled Data from 16 Case-Control Studies
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
Primary Melanoma Tumors from CDKN2A Mutation Carriers Do Not Belong to a Distinct Molecular Subclass
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
A variant in FTO shows association with melanoma risk not due to BMI
Perceptions of genetic research and testing among members of families with an increased risk of malignant melanoma
Genome-wide association study identifies three new melanoma susceptibility loci
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study