Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

At least 17 genomic regions are established as harboring melanoma susceptibility variants, in most instances with genome-wide levels of significance and replication in independent samples. Based on genome-wide single nucleotide polymorphism (SNP) data augmented by imputation to the 1,000 Genomes ref...

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Detalles Bibliográficos
Autores principales: Barrett, Jennifer H, Taylor, John C, Bright, Chloe, Harland, Mark, Dunning, Alison M, Akslen, Lars A, Andresen, Per A, Avril, Marie-Françoise, Azizi, Esther, Bianchi Scarrà, Giovanna, Brossard, Myriam, Brown, Kevin M, Dębniak, Tadeusz, Elder, David E, Friedman, Eitan, Ghiorzo, Paola, Gillanders, Elizabeth M, Gruis, Nelleke A, Hansson, Johan, Helsing, Per, Hočevar, Marko, Höiom, Veronica, Ingvar, Christian, Landi, Maria Teresa, Lang, Julie, Lathrop, G Mark, Lubiński, Jan, Mackie, Rona M, Molven, Anders, Novaković, Srdjan, Olsson, Håkan, Puig, Susana, Puig-Butille, Joan Anton, van der Stoep, Nienke, van Doorn, Remco, van Workum, Wilbert, Goldstein, Alisa M, Kanetsky, Peter A, Pharoah, Paul D P, Demenais, Florence, Hayward, Nicholas K, Newton Bishop, Julia A, Bishop, D Timothy, Iles, Mark M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Cancer Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328144/
https://www.ncbi.nlm.nih.gov/pubmed/25077817
http://dx.doi.org/10.1002/ijc.29099

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