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Times Co-cited
Similarity
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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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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25
Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
Ching-Ni Jenny Njauw, Ivana Kim, Adriano Piris, Michele Gabree, Michael Taylor, Anne Marie Lane, Margaret M DeAngelis, Evangelos Gragoudas, Lyn M Duncan, Hensin Tsao. PLoS One 2012
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Selection criteria for genetic assessment of patients with familial melanoma.
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Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors.
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Highly recurrent TERT promoter mutations in human melanoma.
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MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis.
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Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma.
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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers.
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Genome-wide association study identifies three new melanoma susceptibility loci.
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Update in genetic susceptibility in 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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Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.
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A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation.
Anders Molven, Magne B Grimstvedt, Solrun J Steine, Mark Harland, Marie-Françoise Avril, Nicholas K Hayward, Lars A Akslen. Genes Chromosomes Cancer 2005
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Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.
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15
Frequent mutation of BAP1 in metastasizing uveal melanomas.
J William Harbour, Michael D Onken, Elisha D O Roberson, Shenghui Duan, Li Cao, Lori A Worley, M Laurin Council, Katie A Matatall, Cynthia Helms, Anne M Bowcock. Science 2010
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15
High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
Hildur Helgadottir, Veronica Höiom, Göran Jönsson, Rainer Tuominen, Christian Ingvar, Ake Borg, Håkan Olsson, Johan Hansson. J Med Genet 2014
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Genetics of familial melanoma: 20 years after CDKN2A.
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High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families.
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A landscape of driver mutations in melanoma.
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BAP1 and cancer.
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13
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
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40
Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma.
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12
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
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Genome-wide association study identifies three loci associated with melanoma risk.
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12
MC1R variants, melanoma and red hair color phenotype: a meta-analysis.
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12
CDKN2A variants in a population-based sample of Queensland families with melanoma.
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12
Germline mutations in shelterin complex genes are associated with familial glioma.
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12
Germline TERT promoter mutations are rare in familial melanoma.
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Identification, genetic testing, and management of hereditary melanoma.
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Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas.
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Germline BAP1 mutations predispose to malignant mesothelioma.
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Mutations in GNA11 in uveal melanoma.
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High frequency of BRAF mutations in nevi.
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Distinct sets of genetic alterations in 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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11
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.