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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitisLoss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizationsGenome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanismsCompare and Contrast Meta Analysis (CCMA): A Method for Identification of Pleiotropic Loci in Genome-Wide Association StudiesTmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjectsCharacterization of Spink6 in mouse skin: the conserved inhibitor of kallikrein-related peptidases is reduced by barrier injuryToward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data.Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk.Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis.Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitisLoss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel.Tobacco smoking leads to extensive genome-wide changes in DNA methylation.Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures.Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic RiskMeta-analysis identifies seven susceptibility loci involved in the atopic marchMulti-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitisNetwork-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.High-density genotyping study identifies four new susceptibility loci for atopic dermatitis.A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.miR-146b Probably Assists miRNA-146a in the Suppression of Keratinocyte Proliferation and Inflammatory Responses in Psoriasis.Association of Atopic Dermatitis with Cardiovascular Risk Factors and Diseases.An integrated epigenetic and transcriptomic analysis reveals distinct tissue-specific patterns of DNA methylation associated with atopic dermatitis.Predictive value of food sensitization and filaggrin mutations in children with eczema.A 5-year randomized trial on the safety and efficacy of pimecrolimus in atopic dermatitis: a critical appraisal.Filaggrin mutations, atopic eczema, hay fever, and asthma in children.Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes.Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema.Putative association of a TLR9 promoter polymorphism with atopic eczema.Increased efficacy of omalizumab in atopic dermatitis patients with wild-type filaggrin status and higher serum levels of phosphatidylcholines.A comprehensive analysis of the COL29A1 gene does not support a role in eczema.Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma.Results of esophagogastroduodenoscopy in patients with oral squamous cell carcinoma--value of endoscopic screening: 10-year experience.Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms.Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk.Cardiac structural and functional changes during long-term antihypertensive treatment with lacidipine and atenolol in the European Lacidipine Study on Atherosclerosis (ELSA).Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis Risk.Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination.
P50
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P50
description
researcher
@en
wetenschapper
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հետազոտող
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name
Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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type
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Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
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prefLabel
Hansjörg Baurecht
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Hansjörg Baurecht
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Hansjörg Baurecht
@es
Hansjörg Baurecht
@nl
Hansjörg Baurecht
@sl
P1053
C-4035-2013
P106
P31
P496
0000-0002-9265-5594