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81.
Liedén, A.* et al.: Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis. PLoS ONE 7:e49694 (2012)
82.
Paternoster, L.* et al.: Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nat. Genet. 44, 187-192 (2012)
83.
Pattaro, C.* et al.: Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet. 8:e1002584 (2012)
84.
Rebane, A.* et al.: Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis. J. Allergy Clin. Immunol. 129, 1297-1306 (2012)
85.
Steffens, M.* et al.: Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum. Mol. Genet. 21, 5359-5372 (2012)
86.
Tsoi, L.C.* et al.: Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat. Genet. 44, 1341-1348 (2012)
87.
Del Greco, M, F.* et al.: Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Hum. Mol. Genet. 20, 1660-1671 (2011)
88.
Dolmans, G.H.* et al.: Wnt signaling and Dupuytren's disease. N. Engl. J. Med. 365, 307-317 (2011)
89.
Eyerich, S. et al.: Mutual antagonism of T cells causing psoriasis and atopic eczema. N. Engl. J. Med. 365, 231-238 (2011)
90.
Gieger, C. et al.: New gene functions in megakaryopoiesis and platelet formation. Nature 480, 201-208 (2011)
91.
Melum, E.* et al.: Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Nat. Genet. 43, 17-19 (2011)
92.
Naumann, A.* et al.: A comprehensive analysis of the COL29A1 gene does not support a role in eczema. J. Allergy Clin. Immunol. 127, 1187-1194 (2011)
93.
Nebel, A.* et al.: A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals. Mech. Ageing Dev. 132, 324-330 (2011)
94.
Sanson, M.* et al.: Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum. Mol. Genet. 20, 2897-2904 (2011)
95.
de Kovel, C.G.F.* et al.: Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain 133, 23-32 (2010)
96.
Ellinghaus, E.* et al.: Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Nat. Genet. 42, 991-995 (2010)
97.
Franke, A.* et al.: Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Nat. Genet. 42, 292-294 (2010)
98.
Horn, D.* et al.: Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum. Mutat. 31, E1851-E1860 (2010)
99.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
100.
Liu, J.Z.* et al.: Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat. Genet. 42, 436-440 (2010)