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Times Cited: 58
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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41
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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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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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
Sara Raimondi, Francesco Sera, Sara Gandini, Simona Iodice, Saverio Caini, Patrick Maisonneuve, Maria Concetta Fargnoli. Int J Cancer 2008
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High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
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Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma.
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MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations.
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Geographical variation in the penetrance of CDKN2A mutations for melanoma.
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Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden.
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TERT promoter mutations in familial and sporadic melanoma.
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Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants.
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Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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Does MC1R genotype convey information about melanoma risk beyond risk phenotypes?
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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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20
POT1 loss-of-function variants predispose to familial melanoma.
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Role of the CDKN2A locus in patients with multiple primary melanomas.
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Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure.
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Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
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Genetics of familial melanoma: 20 years after CDKN2A.
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MC1R germline variants confer risk for BRAF-mutant melanoma.
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15
Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations.
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15
Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles.
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15
Genome-wide association study identifies three loci associated with melanoma risk.
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Selection criteria for genetic assessment of patients with familial melanoma.
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Germline mutations in BAP1 predispose to melanocytic tumors.
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MITF: master regulator of melanocyte development and melanoma oncogene.
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MC1R variation and melanoma risk in the Swedish population in relation to clinical and pathological parameters.
Veronica Höiom, Rainer Tuominen, Max Käller, Diana Lindén, Afshin Ahmadian, Eva Månsson-Brahme, Suzanne Egyhazi, Klas Sjöberg, Joakim Lundeberg, Johan Hansson. Pigment Cell Melanoma Res 2009
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CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
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Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.
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13
Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
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13
MC1R is a potent regulator of PTEN after UV exposure in melanocytes.
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13
High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
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16
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project.
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MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.
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12
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12
Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries.
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MC1R variants increase risk of melanomas harboring BRAF mutations.
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12
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.