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Genome-wide association analysis identifies three psoriasis susceptibility loci

To identify novel psoriasis susceptibility loci, we carried out a meta-analysis of two recent genome-wide association studies 1,2, yielding a discovery sample of 1,831 cases and 2,546 controls. 102 of the most promising loci in the discovery analysis were followed up in a three-stage replication stu...

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Autores principales: Stuart, Philip E., Nair, Rajan P., Ellinghaus, Eva, Ding, Jun, Tejasvi, Trilokraj, Gudjonsson, Johann E., Li, Yun, Weidinger, Stephan, Eberlein, Bernadette, Gieger, Christian, Wichmann, H. Erich, Kunz, Manfred, Ike, Robert, Krueger, Gerald G., Bowcock, Anne M., Mroweitz, Ulrich, Lim, Henry W., Voorhees, John J., Abecasis, Goncalo R., Weichenthal, Michael, Franke, Andre, Rahman, Proton, Gladman, Dafna D., Elder, James T.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965799/
https://www.ncbi.nlm.nih.gov/pubmed/20953189
http://dx.doi.org/10.1038/ng.693
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author Stuart, Philip E.
Nair, Rajan P.
Ellinghaus, Eva
Ding, Jun
Tejasvi, Trilokraj
Gudjonsson, Johann E.
Li, Yun
Weidinger, Stephan
Eberlein, Bernadette
Gieger, Christian
Wichmann, H. Erich
Kunz, Manfred
Ike, Robert
Krueger, Gerald G.
Bowcock, Anne M.
Mroweitz, Ulrich
Lim, Henry W.
Voorhees, John J.
Abecasis, Goncalo R.
Weichenthal, Michael
Franke, Andre
Rahman, Proton
Gladman, Dafna D.
Elder, James T.
author_facet Stuart, Philip E.
Nair, Rajan P.
Ellinghaus, Eva
Ding, Jun
Tejasvi, Trilokraj
Gudjonsson, Johann E.
Li, Yun
Weidinger, Stephan
Eberlein, Bernadette
Gieger, Christian
Wichmann, H. Erich
Kunz, Manfred
Ike, Robert
Krueger, Gerald G.
Bowcock, Anne M.
Mroweitz, Ulrich
Lim, Henry W.
Voorhees, John J.
Abecasis, Goncalo R.
Weichenthal, Michael
Franke, Andre
Rahman, Proton
Gladman, Dafna D.
Elder, James T.
author_sort Stuart, Philip E.
collection PubMed
description To identify novel psoriasis susceptibility loci, we carried out a meta-analysis of two recent genome-wide association studies 1,2, yielding a discovery sample of 1,831 cases and 2,546 controls. 102 of the most promising loci in the discovery analysis were followed up in a three-stage replication study using 4,064 cases and 4,685 controls from Michigan, Toronto, Newfoundland, and Germany. Association at a genome-wide level of significance for the combined discovery and replication samples was found for three genomic regions. One contains NOS2 (rs4795067, p = 4 × 10(−11)), another contains FBXL19 (rs10782001, p = 9 × 10(−10)), and a third contains PSMA6 and NFKBIA (rs12586317, p = 2 × 10(−8)). All three loci were also strongly associated with the subphenotypes of psoriatic arthritis and purely cutaneous psoriasis. Finally, we confirmed a recently identified3 association signal near RNF114.
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spelling pubmed-29657992011-05-01 Genome-wide association analysis identifies three psoriasis susceptibility loci Stuart, Philip E. Nair, Rajan P. Ellinghaus, Eva Ding, Jun Tejasvi, Trilokraj Gudjonsson, Johann E. Li, Yun Weidinger, Stephan Eberlein, Bernadette Gieger, Christian Wichmann, H. Erich Kunz, Manfred Ike, Robert Krueger, Gerald G. Bowcock, Anne M. Mroweitz, Ulrich Lim, Henry W. Voorhees, John J. Abecasis, Goncalo R. Weichenthal, Michael Franke, Andre Rahman, Proton Gladman, Dafna D. Elder, James T. Nat Genet Article To identify novel psoriasis susceptibility loci, we carried out a meta-analysis of two recent genome-wide association studies 1,2, yielding a discovery sample of 1,831 cases and 2,546 controls. 102 of the most promising loci in the discovery analysis were followed up in a three-stage replication study using 4,064 cases and 4,685 controls from Michigan, Toronto, Newfoundland, and Germany. Association at a genome-wide level of significance for the combined discovery and replication samples was found for three genomic regions. One contains NOS2 (rs4795067, p = 4 × 10(−11)), another contains FBXL19 (rs10782001, p = 9 × 10(−10)), and a third contains PSMA6 and NFKBIA (rs12586317, p = 2 × 10(−8)). All three loci were also strongly associated with the subphenotypes of psoriatic arthritis and purely cutaneous psoriasis. Finally, we confirmed a recently identified3 association signal near RNF114. 2010-10-17 2010-11 /pmc/articles/PMC2965799/ /pubmed/20953189 http://dx.doi.org/10.1038/ng.693 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Stuart, Philip E.
Nair, Rajan P.
Ellinghaus, Eva
Ding, Jun
Tejasvi, Trilokraj
Gudjonsson, Johann E.
Li, Yun
Weidinger, Stephan
Eberlein, Bernadette
Gieger, Christian
Wichmann, H. Erich
Kunz, Manfred
Ike, Robert
Krueger, Gerald G.
Bowcock, Anne M.
Mroweitz, Ulrich
Lim, Henry W.
Voorhees, John J.
Abecasis, Goncalo R.
Weichenthal, Michael
Franke, Andre
Rahman, Proton
Gladman, Dafna D.
Elder, James T.
Genome-wide association analysis identifies three psoriasis susceptibility loci
title Genome-wide association analysis identifies three psoriasis susceptibility loci
title_full Genome-wide association analysis identifies three psoriasis susceptibility loci
title_fullStr Genome-wide association analysis identifies three psoriasis susceptibility loci
title_full_unstemmed Genome-wide association analysis identifies three psoriasis susceptibility loci
title_short Genome-wide association analysis identifies three psoriasis susceptibility loci
title_sort genome-wide association analysis identifies three psoriasis susceptibility loci
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965799/
https://www.ncbi.nlm.nih.gov/pubmed/20953189
http://dx.doi.org/10.1038/ng.693
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