Marina Juraleviciute, Joanna Pozniak, Jérémie Nsengimana, Mark Harland, Juliette Randerson-Moor, Patrik Wernhoff, Assia Bassarova, Geir Frode Øy, Gunhild Trøen, Vivi Ann Flørenes, David Timothy Bishop, Meenhard Herlyn, Julia Newton-Bishop, Ana Slipicevic. Pigment Cell Melanoma Res 2020
Times Cited: 8
Times Cited: 8
Times Cited
Times Co-cited
Similarity
Genome-wide association study identifies three loci associated with melanoma risk.
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Genome-wide association study identifies three new melanoma susceptibility loci.
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Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma.
Jiyeon Choi, Tongwu Zhang, Andrew Vu, Julien Ablain, Matthew M Makowski, Leandro M Colli, Mai Xu, Rebecca C Hennessey, Jinhu Yin, Harriet Rothschild,[...]. Nat Commun 2020
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Mx GTPases: dynamin-like antiviral machines of innate immunity.
Otto Haller, Peter Staeheli, Martin Schwemmle, Georg Kochs. Trends Microbiol 2015
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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.
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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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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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STAR: ultrafast universal RNA-seq aligner.
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Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
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Inhibition of nuclear import and cell-cycle progression by mutated forms of the dynamin-like GTPase MxB.
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Human MX2 is an interferon-induced post-entry inhibitor of HIV-1 infection.
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The R package Rsubread is easier, faster, cheaper and better for alignment and quantification of RNA sequencing reads.
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MX2 is an interferon-induced inhibitor of HIV-1 infection.
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
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Inherited genetic variants associated with occurrence of multiple primary melanoma.
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Overexpression of human MX2 gene suppresses cell proliferation, migration, and invasion via ERK/P38/NF-κB pathway in glioblastoma cells.
Huanyu Wang, Qiang Guan, Yang Nan, Quanfeng Ma, Yue Zhong. J Cell Biochem 2019
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A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.
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Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
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edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
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Genetic effects on gene expression across human tissues.
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Association analysis identifies 65 new breast cancer risk loci.
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Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies.
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Melanocytes as instigators and victims of oxidative stress.
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Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits.
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Fast and efficient QTL mapper for thousands of molecular phenotypes.
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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
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Hypomethylation of a LINE-1 promoter activates an alternate transcript of the MET oncogene in bladders with cancer.
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Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
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The histone methyltransferase SETDB1 is recurrently amplified in melanoma and accelerates its onset.
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Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait.
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YY1 regulates melanocyte development and function by cooperating with MITF.
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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.