PuSH - Publication Server of Helmholtz Zentrum München

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21.
Flachsbart, F.* et al.: Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Aging Cell 15, 585-588 (2016)
22.
Manz, J. et al.: Targeted resequencing and functional testing identifies low-frequency missense variants in the gene encoding GARP as significant contributors to atopic dermatitis risk. J. Invest. Dermatol. 136, 2380-2386 (2016)
23.
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
24.
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)
25.
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)
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Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease. N. Engl. J. Med. 374, 1134-1144 (2016)
27.
Stitziel, N.O.* et al.: Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease (vol 374, pg 1134, 2016). N. Engl. J. Med. 374, 1898-1898 (2016)
28.
van Rheenen, W.* et al.: Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat. Genet. 48, 1043-1048 (2016)
29.
Interleukin 1 Genetics Consortium et al.: Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A mendelian randomisation analysis. Lancet Diabet. Endocrinol. 3, 243-253 (2015)
30.
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)
31.
Dankowski, T.* et al.: Exome array GWAS in 10,000 Germans identifies association between MUC22 and multiple sclerosis. Hum. Hered. 79, 32-33 (2015)
32.
Dankowski, T.* et al.: Successful replication of GWAS hits for multiple sclerosis in 10,000 Germans using the exome array. Genet. Epidemiol. 39, 601-608 (2015)
33.
Fischer, A.* et al.: Identification of immune-relevant factors conferring sarcoidosis genetic risk. Am. J. Respir. Crit. Care Med. 192, 727-736 (2015)
34.
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
35.
Goyette, P.* et al.: High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat. Genet. 47, 172-179 (2015)
36.
Kato, N.* et al.: Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282-1293 (2015)
37.
Koch, M.* et al.: Psoriasis and cardiometabolic traits: Modest association but distinct genetic architectures. J. Invest. Dermatol. 135, 1283-1293 (2015)
38.
Kunz, M.* et al.: Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus. Exp. Dermatol. 24, 510-515 (2015)
39.
Lal, D.* et al.: Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS Genet. 11:e1005226 (2015)
40.
Li, J.* et al.: Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Nat. Commun. 6:6804 (2015)