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

Nature Genetics

Volumn 41, Issue 5, 2009, Pages 596-601

  Esparza Gordillo, Jorge ^a,b   Weidinger, Stephan ^c   Fölster Holst, Regina ^d   Bauerfeind, Anja ^b   Ruschendorf, Franz ^b   Patone, Giannino ^b   Rohde, Klaus ^b   Marenholz, Ingo ^a,b   Schulz, Florian ^a,b   Kerscher, Tamara ^a,b   Hubner, Norbert ^b   Wahn, Ulrich ^a   Schreiber, Stefan ^e   Franke, Andre ^e   Vogler, Rainer ^e   Heath, Simon ^f   Baurecht, Hansjörg ^c,g   Novak, Natalija ^h   Rodriguez, Elke ^c   Illig, Thomas ⁱ   Lee Kirsch, Min Ae ^j   Ciechanowicz, Andrzej ^k   Kurek, Michael ^k   Piskackova, Tereza ^l   MacEk, Milan ^a,b   Lee, Young Ae ^a,b   Ruether, Andreas ^e   more..

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^d UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^e UNIVERSITY OF KIEL   (Germany)

^f CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^g TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^h UNIVERSITY OF BONN   (Germany)

ⁱ INSTITUTE OF EPIDEMIOLOGY   (Germany)

^j DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^k POMERANIAN MEDICAL UNIVERSITY   (Poland)

^l UNIVERSITY HOSPITAL MOTOL   (Czech Republic)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CETIRIZINE; LEVOCETIRIZINE;

ALLELE; ARTICLE; ASTHMA; ATOPIC DERMATITIS; CHILD; CHROMOSOME 11Q; CHROMOSOME REPLICATION; CHROMOSOME VARIANT; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DOWNSTREAM PROCESSING; EUROPE; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOME ANALYSIS; GEOGRAPHIC ORIGIN; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; NUCLEAR FAMILY; PRIORITY JOURNAL; RISK FACTOR; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 11; DERMATITIS, ATOPIC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME, HUMAN; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 67349252610     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.347     Document Type: Article

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