@article{3102881,
    title = "MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M-SKIP project",
    author = "Stefanaki, I. and Stratigos, A.J. and Kypreou, K.P. and Evangelou, E. and Gandini, S. and Maisonneuve, P. and Polsky, D. and Lazovich, D. and Newton-Bishop, J. and Kanetsky, P.A. and Puig, S. and Gruis, N.A. and Ghiorzo, P. and Pellegrini, C. and De Nicolo, A. and Ribas, G. and Guida, G. and Garcia-Borron, J.C. and Fargnoli, M.C. and Nan, H. and Landi, M.T. and Little, J. and Sera, F. and Raimondi, S. and for the M-SKIP Study Group",
    journal = "Journal of the European Academy of Dermatology and Venereology",
    year = "2021",
    volume = "35",
    number = "2",
    pages = "e135-e138",
    publisher = "Wiley-Blackwell Publishing Ltd",
    issn = "0926-9959, 1468-3083",
    doi = "10.1111/jdv.16869",
    keywords = "melanocortin 1 receptor;  melanocortin 1 receptor, allele;  cancer risk;  cutaneous melanoma;  dysplastic nevus;  genetic association;  genetic variability;  human;  hyperpigmentation;  Letter;  MC1R gene;  melanoma;  nevus;  sun exposure;  case control study;  genetics;  meta analysis;  pigmented nevus;  risk factor;  skin tumor, Case-Control Studies;  Humans;  Melanoma;  Nevus, Pigmented;  Receptor, Melanocortin, Type 1;  Risk Factors;  Skin Neoplasms"
}