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Times Cited: 279
Times Cited: 279
Times Cited
Times Co-cited
Similarity
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
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Geographical variation in the penetrance of CDKN2A mutations for melanoma.
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Germline p16 mutations in familial melanoma.
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TERT promoter mutations in familial and sporadic melanoma.
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Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma.
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POT1 loss-of-function variants predispose to familial melanoma.
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Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families.
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Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations.
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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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Selection criteria for genetic assessment of patients with familial melanoma.
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
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High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
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Germline mutations in BAP1 predispose to melanocytic tumors.
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High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families.
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Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling.
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Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations.
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Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.
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Update in genetic susceptibility in melanoma.
Miriam Potrony, Celia Badenas, Paula Aguilera, Joan Anton Puig-Butille, Cristina Carrera, Josep Malvehy, Susana Puig. Ann Transl Med 2015
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13
Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.
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12
Highly recurrent TERT promoter mutations in human melanoma.
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12
Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors.
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12
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families.
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Identification, genetic testing, and management of hereditary melanoma.
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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
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21
Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers.
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MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis.
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18
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
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42
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study.
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11
A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family.
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10
Germline mutations in shelterin complex genes are associated with familial glioma.
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10
Genome-wide association study identifies three new melanoma susceptibility loci.
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10
Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling.
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12
Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.
Eve Maubec, Valérie Chaudru, Hamida Mohamdi, Christophe Blondel, Patricia Margaritte-Jeannin, Sébastien Forget, Eve Corda, Françoise Boitier, Stéphane Dalle, Pierre Vabres,[...]. J Am Acad Dermatol 2012
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52
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
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10
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.