Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

In order to search for sequence variants conferring risk of thyroid cancer we conducted a genome-wide association study in 192 and 37,196 Icelandic cases and controls, respectively, followed by a replication study in individuals of European descent. Here we show that two common variants, located on...

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Main Authors: Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F, Jonasson, Jon G, Sigurdsson, Asgeir, Bergthorsson, Jon T, He, Huiling, Blondal, Thorarinn, Geller, Frank, Jakobsdottir, Margret, Magnusdottir, Droplaug N, Matthiasdottir, Sigurborg, Stacey, Simon N, Skarphedinsson, Oskar B, Helgadottir, Hafdis, Li, Wei, Nagy, Rebecca, Aguillo, Esperanza, Faure, Eduardo, Prats, Enrique, Saez, Berta, Martinez, Mariano, Eyjolfsson, Gudmundur I, Bjornsdottir, Unnur S, Holm, Hilma, Kristjansson, Kristleifur, Frigge, Michael L, Kristvinsson, Hoskuldur, Gulcher, Jeffrey R, Jonsson, Thorvaldur, Rafnar, Thorunn, Hjartarsson, Hannes, Mayordomo, Jose I, de la Chapelle, Albert, Hrafnkelsson, Jon, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3664837/
https://ncbi.nlm.nih.gov/pubmed/19198613
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.339
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