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Melanoma Research|July 16, 2014
Blood DNA methylation, nevi number, and the risk of melanomaLaura Pergoli, Chiara Favero, Ruth M Pfeiffer, et al.Journal of the National Cancer Institute|July 7, 2005
MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean populationMaria Teresa Landi, Peter A Kanetsky, Shirley Tsang, et al.Plos Genetics|November 16, 2019
Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing StudiesAndrew Schlafly, Ruth M Pfeiffer, Eduardo Nagore, et al.Pigment Cell & Melanoma Research|January 10, 2012
Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone familyXiaohong R Yang, Kevin Brown, Maria T Landi, et al.Journal of the American Academy of Dermatology|April 14, 2020
Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and SpainMichael R Sargen, Donato Calista, David E Elder, et al.The Journal of Investigative Dermatology|March 28, 2008
MC1R variants increase risk of melanomas harboring BRAF mutationsMaria Concetta Fargnoli, Maria Concetia Fargnoli, Kris Pike, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|August 12, 2018
MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortiumAlexander J Stratigos, Maria Concetta Fargnoli, Arcangela De Nicolo, et al.The Journal of Investigative Dermatology|July 30, 2013
Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone familiesXueying Liang, Ruth M Pfeiffer, Wen-Qing Li, et al.Plos One|January 10, 2013
On the interplay of telomeres, nevi and the risk of melanomaClara Bodelon, Ruth M Pfeiffer, Valentina Bollati, et al.Familial Cancer|July 3, 2021
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone familyKevin M Brown, Mai Xu, Michael Sargen, et al.Pageof 4