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Times Cited: 183
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Times Co-cited
Similarity
Genome-wide association study identifies three loci associated with melanoma risk.
D Timothy Bishop, Florence Demenais, Mark M Iles, Mark Harland, John C Taylor, Eve Corda, Juliette Randerson-Moor, Joanne F Aitken, Marie-Francoise Avril, Esther Azizi,[...]. Nat Genet 2009
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Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
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Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
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Common sequence variants on 20q11.22 confer melanoma susceptibility.
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Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
Thorunn Rafnar, Patrick Sulem, Simon N Stacey, Frank Geller, Julius Gudmundsson, Asgeir Sigurdsson, Margret Jakobsdottir, Hafdis Helgadottir, Steinunn Thorlacius, Katja K H Aben,[...]. Nat Genet 2009
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A variant in FTO shows association with melanoma risk not due to BMI.
Mark M Iles, Matthew H Law, Simon N Stacey, Jiali Han, Shenying Fang, Ruth Pfeiffer, Mark Harland, Stuart Macgregor, John C Taylor, Katja K Aben,[...]. Nat Genet 2013
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A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
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Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
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Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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TERT promoter mutations in familial and sporadic melanoma.
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
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Genetic determinants of hair, eye and skin pigmentation in Europeans.
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POT1 loss-of-function variants predispose to familial melanoma.
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Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.
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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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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.
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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.
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Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.
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Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma.
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A landscape of driver mutations in melanoma.
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Inherited genetic variants associated with occurrence of multiple primary melanoma.
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Melanocytic nevi, nevus genes, and melanoma risk in a large case-control study in the United Kingdom.
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Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
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Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.
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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.