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Times Cited: 65
Times Cited: 65
Times Cited
Times Co-cited
Similarity
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Hamida Mohamdi, Audrey Remenieras,[...]. Nature 2011
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Satoru Yokoyama, Susan L Woods, Glen M Boyle, Lauren G Aoude, Stuart MacGregor, Victoria Zismann, Michael Gartside, Anne E Cust, Rizwan Haq, Mark Harland,[...]. Nature 2011
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Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients.
Richard A Sturm, Carly Fox, Phil McClenahan, Kasturee Jagirdar, Maider Ibarrola-Villava, Parastoo Banan, Nicola C Abbott, Gloria Ribas, Brian Gabrielli, David L Duffy,[...]. J Invest Dermatol 2014
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40
TERT promoter mutations in familial and sporadic melanoma.
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MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Jianxin Shi, Xiaohong R Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-de Paillerets, Eduardo Nagore, Marie Francoise Avril,[...]. Nat Genet 2014
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POT1 loss-of-function variants predispose to familial melanoma.
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Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants.
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Hanne Eknes Puntervoll, Xiaohong R Yang, Hildegunn Høberg Vetti, Ingeborg M Bachmann, Marie Françoise Avril, Meriem Benfodda, Caterina Catricalà, Stéphane Dalle, Anne B Duval-Modeste, Paola Ghiorzo,[...]. J Med Genet 2013
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High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
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Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
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Germline mutations in BAP1 predispose to melanocytic tumors.
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Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma.
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
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Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations.
Miriam Potrony, Joan Anton Puig-Butille, Paula Aguilera, Celia Badenas, Gemma Tell-Marti, Cristina Carrera, Luis Javier Del Pozo, Julian Conejo-Mir, Josep Malvehy, Susana Puig. JAMA Dermatol 2016
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Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.
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Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma.
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BAP1 and cancer.
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Fifteen-year quest for microphthalmia-associated transcription factor target genes.
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MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis.
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Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
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High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
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Clinical genetic testing for familial melanoma in Italy: a cooperative study.
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Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma.
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25
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
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13
Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors.
Sara Gandini, Francesco Sera, Maria Sofia Cattaruzza, Paolo Pasquini, Roberto Zanetti, Cinzia Masini, Peter Boyle, Carmelo Francesco Melchi. Eur J Cancer 2005
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13
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
Mohamed H Abdel-Rahman, Robert Pilarski, Colleen M Cebulla, James B Massengill, Benjamin N Christopher, Getachew Boru, Peter Hovland, Frederick H Davidorf. J Med Genet 2011
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13
Selection criteria for genetic assessment of patients with familial melanoma.
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13
Highly recurrent TERT promoter mutations in human melanoma.
Franklin W Huang, Eran Hodis, Mary Jue Xu, Gregory V Kryukov, Lynda Chin, Levi A Garraway. Science 2013
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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
Miriam Potrony, Celia Badenas, Paula Aguilera, Joan Anton Puig-Butille, Cristina Carrera, Josep Malvehy, Susana Puig. Ann Transl Med 2015
13
Clinicopathological features of and risk factors for multiple primary melanomas.
Cristina R Ferrone, Leah Ben Porat, Katherine S Panageas, Marianne Berwick, Allan C Halpern, Ami Patel, Daniel G Coit. JAMA 2005
Cristina R Ferrone, Leah Ben Porat, Katherine S Panageas, Marianne Berwick, Allan C Halpern, Ami Patel, Daniel G Coit. JAMA 2005
12
Role of the CDKN2A locus in patients with multiple primary melanomas.
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CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
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Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.
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12
Germline BAP1 mutations predispose to renal cell carcinomas.
Tatiana Popova, Lucie Hebert, Virginie Jacquemin, Sophie Gad, Virginie Caux-Moncoutier, Catherine Dubois-d'Enghien, Bénédicte Richaudeau, Xavier Renaudin, Jason Sellers, André Nicolas,[...]. Am J Hum Genet 2013
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12
MC1R variants, melanoma and red hair color phenotype: a meta-analysis.
Sara Raimondi, Francesco Sera, Sara Gandini, Simona Iodice, Saverio Caini, Patrick Maisonneuve, Maria Concetta Fargnoli. Int J Cancer 2008
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12
Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases.
K Rai, R Pilarski, C M Cebulla, M H Abdel-Rahman. Clin Genet 2016
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Hereditary melanoma: Update on syndromes and management: Emerging melanoma cancer complexes and genetic counseling.
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Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF.
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MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations.
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10
Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma.
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10
Sumoylation modulates transcriptional activity of MITF in a promoter-specific manner.
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Microphthalmia-associated transcription factor controls the DNA damage response and a lineage-specific senescence program in melanomas.
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10
Germline BAP1 mutations predispose to malignant mesothelioma.
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10
Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure.
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10
Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.
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Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study.
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CDKN2A is the main susceptibility gene in Italian pancreatic cancer families.
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14
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.