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Times Cited: 156
Times Cited: 156
Times Cited
Times Co-cited
Similarity
Genome-wide association study identifies three new melanoma susceptibility loci.
Jennifer H Barrett, Mark M Iles, Mark Harland, John C Taylor, Joanne F Aitken, Per Arne Andresen, Lars A Akslen, Bruce K Armstrong, Marie-Francoise Avril, Esther Azizi,[...]. Nat Genet 2011
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Genome-wide association study identifies three loci associated with melanoma risk.
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Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Stuart Macgregor, Grant W Montgomery, Jimmy Z Liu, Zhen Zhen Zhao, Anjali K Henders, Mitchell Stark, Helen Schmid, Elizabeth A Holland, David L Duffy, Mingfeng Zhang,[...]. Nat Genet 2011
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Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
Matthew H Law, D Timothy Bishop, Jeffrey E Lee, Myriam Brossard, Nicholas G Martin, Eric K Moses, Fengju Song, Jennifer H Barrett, Rajiv Kumar, Douglas F Easton,[...]. Nat Genet 2015
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Common sequence variants on 20q11.22 confer melanoma susceptibility.
Kevin M Brown, Stuart Macgregor, Grant W Montgomery, David W Craig, Zhen Zhen Zhao, Kelly Iyadurai, Anjali K Henders, Nils Homer, Megan J Campbell, Mitchell Stark,[...]. Nat Genet 2008
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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
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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Exonuclease 1 (EXO1) gene variation and melanoma risk.
Fengju Song, Abrar A Qureshi, Jiangwen Zhang, Christopher I Amos, Jeffrey E Lee, Qingyi Wei, Jiali Han. DNA Repair (Amst) 2012
Fengju Song, Abrar A Qureshi, Jiangwen Zhang, Christopher I Amos, Jeffrey E Lee, Qingyi Wei, Jiali Han. DNA Repair (Amst) 2012
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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.
Yun Li, Cristen J Willer, Jun Ding, Paul Scheet, Gonçalo R Abecasis. Genet Epidemiol 2010
Yun Li, Cristen J Willer, Jun Ding, Paul Scheet, Gonçalo R Abecasis. Genet Epidemiol 2010
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Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma.
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Final version of 2009 AJCC melanoma staging and classification.
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The NCBI dbGaP database of genotypes and phenotypes.
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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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A variant in FTO shows association with melanoma risk not due to BMI.
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Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
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Transcriptome and genome sequencing uncovers functional variation in humans.
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MC1R variants, melanoma and red hair color phenotype: a meta-analysis.
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A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.
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An integrated map of genetic variation from 1,092 human genomes.
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TERT promoter mutations in familial and sporadic melanoma.
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
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Assessing the probability that a positive report is false: an approach for molecular epidemiology studies.
Sholom Wacholder, Stephen Chanock, Montserrat Garcia-Closas, Laure El Ghormli, Nathaniel Rothman. J Natl Cancer Inst 2004
Sholom Wacholder, Stephen Chanock, Montserrat Garcia-Closas, Laure El Ghormli, Nathaniel Rothman. J Natl Cancer Inst 2004
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
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Joint effect of multiple common SNPs predicts melanoma susceptibility.
Shenying Fang, Jiali Han, Mingfeng Zhang, Li-e Wang, Qingyi Wei, Christopher I Amos, Jeffrey E Lee. PLoS One 2013
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Two newly identified genetic determinants of pigmentation in Europeans.
Patrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, Agnar Helgason, Thorunn Rafnar, Margret Jakobsdottir, Stacy Steinberg, Sigurjon A Gudjonsson, Arnar Palsson, Gudmar Thorleifsson,[...]. Nat Genet 2008
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9
Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.
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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
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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A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.
Richard A Sturm, David L Duffy, Zhen Zhen Zhao, Fabio P N Leite, Mitchell S Stark, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. Am J Hum Genet 2008
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Assessment of genotype imputation methods.
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Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.
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Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
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An ultraviolet-radiation-independent pathway to melanoma carcinogenesis in the red hair/fair skin background.
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Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles.
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Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population.
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
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Melanoma genetics: recent findings take us beyond well-traveled pathways.
Matthew H Law, Stuart Macgregor, Nicholas K Hayward. J Invest Dermatol 2012
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial 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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Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma.
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Melanocortin 1 receptor (MC1R) gene variants are associated with an increased risk for cutaneous melanoma which is largely independent of skin type and hair color.
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Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.
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GenABEL: an R library for genome-wide association analysis.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma.
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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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SLC45A2: a novel malignant melanoma-associated gene.
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POT1 loss-of-function variants predispose to familial melanoma.
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7
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.