A common variant on chromosome 11q13 is associated with atopic dermatitis

We conducted a genome-wide association study in 939 individuals with atopic dermatitis and 975 controls as well as 270 complete nuclear families with two affected siblings. SNPs consistently associated with atopic dermatitis in both discovery sets were then investigated in two additional independent...

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Veröffentlicht in:Nature genetics 2009-05, Vol.41 (5), p.596-601
Hauptverfasser: Patone, Giannino, Macek, Milan, Wahn, Ulrich, Piskackova, Tereza, Franke, Andre, Ruether, Andreas, Bauerfeind, Anja, Esparza-Gordillo, Jorge, Ruschendorf, Franz, Kerscher, Tamara, Vogler, Rainer, Schulz, Florian, Lee, Young-Ae, Ciechanowicz, Andrzej, Fölster-Holst, Regina, Hubner, Norbert, Novak, Natalija, Marenholz, Ingo, Heath, Simon, Rohde, Klaus, Schreiber, Stefan, Kurek, Michael, Lee-Kirsch, Min-Ae, Illig, Thomas, Weidinger, Stephan, Baurecht, Hansjörg, Rodriguez, Elke
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container_issue 5
container_start_page 596
container_title Nature genetics
container_volume 41
creator Patone, Giannino
Macek, Milan
Wahn, Ulrich
Piskackova, Tereza
Franke, Andre
Ruether, Andreas
Bauerfeind, Anja
Esparza-Gordillo, Jorge
Ruschendorf, Franz
Kerscher, Tamara
Vogler, Rainer
Schulz, Florian
Lee, Young-Ae
Ciechanowicz, Andrzej
Fölster-Holst, Regina
Hubner, Norbert
Novak, Natalija
Marenholz, Ingo
Heath, Simon
Rohde, Klaus
Schreiber, Stefan
Kurek, Michael
Lee-Kirsch, Min-Ae
Illig, Thomas
Weidinger, Stephan
Baurecht, Hansjörg
Rodriguez, Elke
description We conducted a genome-wide association study in 939 individuals with atopic dermatitis and 975 controls as well as 270 complete nuclear families with two affected siblings. SNPs consistently associated with atopic dermatitis in both discovery sets were then investigated in two additional independent replication sets totalling 2,637 cases and 3,957 controls. Highly significant association was found with allele A of rs7927894 on chromosome 11q13.5, located 38 kb downstream of C11orf30 (Pcombined = 7.6 × 10−10). Approximately 13% of individuals of European origin are homozygous for rs7927894[A], and their risk of developing atopic dermatitis is 1.47 times that of noncarriers.
doi_str_mv 10.1038/ng.347
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1546-1718
language eng
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subjects Adolescent
Agriculture
Allergic diseases
Animal Genetics and Genomics
Atopic dermatitis
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Cancer Research
Care and treatment
Case-Control Studies
Chromosomes
Chromosomes, Human, Pair 11 - genetics
Crohn's disease
Data base management
Dermatitis
Dermatitis, Atopic - genetics
DNA damage
DNA repair
Female
Fundamental and applied biological sciences. Psychology
Gene Function
Genetic aspects
Genetic Predisposition to Disease
Genetic susceptibility
Genetic Variation
Genetics
Genetics of eukaryotes. Biological and molecular evolution
Genome, Human
Health aspects
Human Genetics
Humans
Immunopathology
Independent sample
letter
Linkage Disequilibrium
Male
Medical sciences
Polymorphism, Single Nucleotide
Principal components analysis
Risk factors
Single nucleotide polymorphisms
Skin allergic diseases. Stinging insect allergies
Studies
Young Adult
title A common variant on chromosome 11q13 is associated with atopic dermatitis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T06%3A39%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20common%20variant%20on%20chromosome%2011q13%20is%20associated%20with%20atopic%20dermatitis&rft.jtitle=Nature%20genetics&rft.au=Patone,%20Giannino&rft.date=2009-05-01&rft.volume=41&rft.issue=5&rft.spage=596&rft.epage=601&rft.pages=596-601&rft.issn=1061-4036&rft.eissn=1546-1718&rft.coden=NGENEC&rft_id=info:doi/10.1038/ng.347&rft_dat=%3Cgale_proqu%3EA199397083%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=222652865&rft_id=info:pmid/19349984&rft_galeid=A199397083&rfr_iscdi=true