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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)
ILLUMINATE 301: A randomized phase III comparison of IMO-2125 with ipilimumab (ipi) versus ipi alone in subjects with anti PD 1 refractory melanoma
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
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project
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
Inherited variation in the PARP1 gene and survival from melanoma
An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study
Somatic BRAF and NRAS Mutations in Familial Melanomas with Known Germline CDKN2A Status: A GenoMEL Study
A variant in FTO shows association with melanoma risk not due to BMI
Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies
Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
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
IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma