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Avril, M.F. 1 Azizi, E. 1 Bergman, W. 1 Bianchi-Scarra, G. 1 Bishop, D.T. 1 Bressac-de Paillerets, B. 1 Calista, D. 1 Carrera, C. 1 Chaudru, V. 1 Demenais, F. 1 Elder, D.E. 1 GenoMEL, 1 Gillanders, E. 1 Goldstein, A.M. 1 Gruis, N. 1 Hansson, J. 1 Harland, M. 1 Hayward, N.K. 1 Hogg, D. 1 Hoiom, V. 1 Holland, E.A. 1 Ingvar, C. 1 Kanetsky, P.A. 1 Landi, M.T. 1 Lang, J. 1 Mackie, R. 1 Mann, G.J. 1 Ming, M.E. 1 Mohamdi, H. 1 Newton Bishop, J.A. 1 Njauw, C.J. 1 Olsson, H. 1 Palmer, J. 1 Pastorino, L. 1 Puig, S. 1 Randerson-Moor, J. 1 Stark, M. 1 Tsao, H. 1 Tucker, M.A. 1 Yang, X.R. 1
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Association of MC1R Variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study
Demenais, F.; Mohamdi, H.; Chaudru, V.; Goldstein, A.M.; … - 2010
Background Carrying the cyclin-dependent kinase inhibitor 2A (CDKN2A) germline mutations is associated with a high risk for melanoma. Penetrance of CDKN2A mutations is modified by pigmentation characteristics, nevus phenotypes, and some variants of the melanocortin-1 receptor gene (MC1R), which...
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