Published in

Nature Research, Nature Genetics, 12(47), p. 1449-1456

DOI: 10.1038/ng.3424



Export citation

Search in Google Scholar

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Journal article published in 2015 by Herman T. den Dekker, Johan C. de Jongste, Maria Pino Yanes, Lavinia Paternoster ORCID, Marie Standl, Feng Li Xiao, David P. Strachan, Johannes Waage, John A. Curtin, Klaus Bønnelykke, Hansjörg Baurecht, Cheng-Jian Xu, Melanie Hotze, Alexessander Couto Alves, Jacob P. Thyssen and other authors.
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO


Genetic association studies have identified 21 loci associated with atopic dermatitis risk predominantly in populations of European ancestry. To identify further susceptibility loci for this common, complex skin disease, we performed a meta-analysis of >15 million genetic variants in 21,399 cases and 95,464 controls from populations of European, African, Japanese and Latino ancestry, followed by replication in 32,059 cases and 228,628 controls from 18 studies. We identified ten new risk loci, bringing the total number of known atopic dermatitis risk loci to 31 (with new secondary signals at four of these loci). Notably, the new loci include candidate genes with roles in the regulation of innate host defenses and T cell function, underscoring the important contribution of (auto)immune mechanisms to atopic dermatitis pathogenesis.