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Times Cited: 93
Times Cited: 93
Times Cited
Times Co-cited
Similarity
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
Mario Falchi, Veronique Bataille, Nicholas K Hayward, David L Duffy, Julia A Newton Bishop, Tomi Pastinen, Alessandra Cervino, Zhen Z Zhao, Panos Deloukas, Nicole Soranzo,[...]. Nat Genet 2009
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Genome-wide association study identifies three loci associated with melanoma risk.
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Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
David L Duffy, Zhen Z Zhao, Richard A Sturm, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. J Invest Dermatol 2010
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A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
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Genetic determinants of hair, eye and skin pigmentation in Europeans.
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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
Daniel F Gudbjartsson, Patrick Sulem, Simon N Stacey, Alisa M Goldstein, Thorunn Rafnar, Bardur Sigurgeirsson, Kristrun R Benediktsdottir, Kristin Thorisdottir, Rafn Ragnarsson, Steinunn G Sveinsdottir,[...]. Nat Genet 2008
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Genome-wide association study identifies three new melanoma susceptibility loci.
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
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Common sequence variants on 20q11.22 confer melanoma susceptibility.
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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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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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A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.
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Two newly identified genetic determinants of pigmentation in Europeans.
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Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.
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Genome-wide association study of tanning phenotype in a population of European ancestry.
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A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes.
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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
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Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study.
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A germline variant in the interferon regulatory factor 4 gene as a novel skin cancer risk locus.
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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.
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Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
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A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.
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Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk.
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Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population.
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Distinct sets of genetic alterations in melanoma.
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A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs.
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
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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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A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.
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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.