2012 (v1)
Publication
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Uploaded on: April 14, 2023
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2013 (v1)Publication
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2007 (v1)Publication
The G101W founder mutation is the most common CDKN2A mutation in Italy, Spain, and France. As the background of modifying genes, environmental exposures, and sun behavior vary across countries, studying G101W carriers from distinct countries offers a unique opportunity to evaluate possible modifying factors in melanoma development. We evaluated...
Uploaded on: October 11, 2023 -
2017 (v1)Publication
Germline mutations in CDKN2A are frequently identified among melanoma kindreds and are associated with increased atypical nevus counts. However, a clear relationship between pathogenic CDKN2A mutation carriage and other nevus phenotypes including counts of common acquired nevi has not yet been established. Using data from GenoMEL, we...
Uploaded on: April 14, 2023