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Ellinghaus, D.* ; Baurecht, H.* ; Esparza-Gordillo, J.* ; Rodriguez, E.* ; Matanovic, A.* ; Marenholz, I.* ; Hubner, N.* ; Schaarschmidt, H.* ; Novak, N.* ; Michel, S.* ; Maintz, L.* ; Werfel, T.* ; Meyer-Hoffert, U.* ; Hotze, M.* ; Prokisch, H. ; Heim, K. ; Herder, C.* ; Hirota, T.* ; Tamari, M.* ; Kubo, M.* ; Takahashi, A.* ; Nakamura, Y.* ; Tsoi, L.C.* ; Stuart, P.* ; Elder, J.T.* ; Sun, L.* ; Zuo, X.* ; Yang, S.* ; Zhang, X.* ; Hoffmann, P.* ; Nöthen, M.M.* ; Fölster-Holst, R.* ; Winkelmann, J. ; Illig, T. ; Boehm, B.O.* ; Duerr, R.H.* ; Büning, C.* ; Brand, S.* ; Glas, J.* ; McAleer, M.A.* ; Fahy, C.M.* ; Kabesch, M.* ; Brown, S.* ; McLean, W.H.* ; Irvine, A.D.* ; Schreiber, S.* ; Lee, Y.A.* ; Franke, A.* ; Weidinger, S.*

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis.

Nat. Genet. 45, 808-812 (2013)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Atopic dermatitis is a common inflammatory skin disease with a strong heritable component. Pathogenetic models consider keratinocyte differentiation defects and immune alterations as scaffolds, and recent data indicate a role for autoreactivity in at least a subgroup of patients. FLG (encoding filaggrin) has been identified as a major locus causing skin barrier deficiency. To better define risk variants and identify additional susceptibility loci, we densely genotyped 2,425 German individuals with atopic dermatitis (cases) and 5,449 controls using the Immunochip array followed by replication in 7,196 cases and 15,480 controls from Germany, Ireland, Japan and China. We identified four new susceptibility loci for atopic dermatitis and replicated previous associations. This brings the number of atopic dermatitis risk loci reported in individuals of European ancestry to 11. We estimate that these susceptibility loci together account for 14.4% of the heritability for atopic dermatitis.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Genome-wide Association ; Crohns-disease ; Myocardial-infarction ; Chromosome 11q13 ; Common Variant ; Celiac-disease ; Psoriatic Skin ; Population ; Asthma ; Gene
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 45, Heft: 7, Seiten: 808-812 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Human Genetics (IHG)
Research Unit Molecular Epidemiology (AME)