PuSH - Publication Server of Helmholtz Zentrum München

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1.
Demenais, F.* et al.: Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat. Genet. 50, 42-53 (2018)
2.
Illi, S. et al.: Farming, cytokines, 17q21 and wheeze in the first year of life. Allergy 73, 107-108 (2018)
3.
Waage, J.* et al.: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50, 1072–1080 (2018)
4.
Waage, J.* et al.: Author correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat. Genet. 50:1343 (2018)
5.
Hose, A.J.* et al.: Latent class analysis reveals clinically relevant atopy phenotypes in 2 birth cohorts. J. Allergy Clin. Immunol. 139, 1935-1945.e12 (2017)
6.
Marenholz, I.* et al.: Genome-wide association study unravels genetic determinants of the atopic march. Allergy 71, 431-431 (2016)
7.
Schieck, M.* et al.: Doublesex and Mab-3 Related Transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages. J. Allergy Clin. Immunol. 138, 421-431 (2016)
8.
Schmitt, J.* et al.: Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes. J. Allergy Clin. Immunol. 137, 130–136 (2016)
9.
Baurecht, H.* et al.: Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. Am. J. Hum. Genet. 96, 104-120 (2015)
10.
Marenholz, I.* et al.: Meta-analysis identifies seven susceptibility loci involved in the atopic march. Nat. Commun. 6:8804 (2015)
11.
Schaarschmidt, H.* et al.: A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis.ϖ J. Allergy Clin. Immunol. 136, 802-806 (2015)
12.
Schedel, M.* et al.: Polymorphisms related to ORMDL3 are associated with asthma susceptibility, alterations in transcriptional regulation of ORMDL3, and changes in TH2 cytokine levels. J. Allergy Clin. Immunol. 136, 893-903 (2015)
13.
Toncheva, A.A.* et al.: Childhood asthma is associated with mutations and gene expression differences of ORMDL genes which can interact. Allergy 70, 1288-1299 (2015)
14.
Hotze, M.* et al.: Genome-wide comparative analysis of atopic eczema and psoriasis gives insight into disease mechanisms. Exp. Dermatol. 23, E21 (2014)
15.
Lluis, A.* et al.: Regulation of TH17 markers early in life through maternal farm exposure. J. Allergy Clin. Immunol. 133, 864-871 (2014)
16.
Schieck, M.* et al.: Genetic variation in TH17 pathway genes, childhood asthma, and total serum IgE levels. J. Allergy Clin. Immunol. 133, 888-891 (2014)
17.
Schieck, M.* et al.: A polymorphism in the TH2 locus control region is associated with changes in DNA methylation and gene expression. Allergy 69, 1171-1180 (2014)
18.
Scholtens, S.* et al.: Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure. J. Allergy Clin. Immunol. 133, 885-888 (2014)
19.
Sharma, V.* et al.: Fine-mapping of IgE-associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data. Allergy 69, 1077-1084 (2014)
20.
Chen, C.-M. & Kabesch, M.*: Gene by environment interaction in respiratory diseases. In: Wilmott, R.* ; Boat, T.* ; Bush, A.* ; Chernick, V.* ; Deterding, R.* ; Ratjen, F.* [Eds.]: Kendig and Chernick's Disorders of the Respiratory Tract in Children. Philadelphia (u.a.): Saunders Elsevier, 2013. 23-28