Hüffmeier U - Search Results

1

Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.

Dand N, Mucha S, Tsoi LC, Mahil SK, Stuart PE, Arnold A, Baurecht H, Burden AD, Callis Duffin K, Chandran V, Curtis CJ, Das S, Ellinghaus D, Ellinghaus E, Enerback C, Esko T, Gladman DD, Griffiths CEM, Gudjonsson JE, Hoffman P, Homuth G, Hüffmeier U, Krueger GG, Laudes M, Lee SH, Lieb W, Lim HW, Löhr S, Mrowietz U, Müller-Nurayid M, Nöthen M, Peters A, Rahman P, Reis A, Reynolds NJ, Rodriguez E, Schmidt CO, Spain SL, Strauch K, Tejasvi T, Voorhees JJ, Warren RB, Weichenthal M, Weidinger S, Zawistowski M, Nair RP, Capon F, Smith CH, Trembath RC, Abecasis GR, Elder JT, Franke A, Simpson MA, Barker JN. Dand N, et al. Among authors: huffmeier u. Hum Mol Genet. 2017 Nov 1;26(21):4301-4313. doi: 10.1093/hmg/ddx328. Hum Mol Genet. 2017. PMID: 28973304 Free PMC article.

2

Tumor necrosis factor receptor-associated periodic syndrome characterized by a mutation affecting the cleavage site of the receptor: implications for pathogenesis.

Kriegel MA, Hüffmeier U, Scherb E, Scheidig C, Geiler T, Kalden JR, Reis A, Lorenz HM. Kriegel MA, et al. Among authors: huffmeier u. Arthritis Rheum. 2003 Aug;48(8):2386-8. doi: 10.1002/art.11169. Arthritis Rheum. 2003. PMID: 12905494 Free article. No abstract available.

3

Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci.

Hensen P, Windemuth C, Hüffmeier U, Rüschendorf F, Stadelmann A, Hoppe V, Fenneker D, Ständer M, Schmitt-Egenolf M, Wienker TF, Traupe H, Reis A. Hensen P, et al. Among authors: huffmeier u. Exp Dermatol. 2003 Aug;12(4):490-6. doi: 10.1034/j.1600-0625.2003.00040.x. Exp Dermatol. 2003. PMID: 12930307

4

Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis.

Hensen P, Asadullah K, Windemuth C, Rüschendorf F, Hüffmeier U, Ständer M, Schmitt-Egenolf M, Wienker TF, Reis A, Traupe H. Hensen P, et al. Among authors: huffmeier u. Br J Dermatol. 2003 Aug;149(2):381-5. doi: 10.1046/j.1365-2133.2003.05411.x. Br J Dermatol. 2003. PMID: 12932247

5

Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohort.

Lascorz J, Burkhardt H, Hüffmeier U, Böhm B, Schürmeyer-Horst F, Lohmann J, Ständer M, Wendler J, Kelsch R, Baumann C, Küster W, Traupe H, Reis A. Lascorz J, et al. Among authors: huffmeier u. Ann Rheum Dis. 2005 Jun;64(6):951-4. doi: 10.1136/ard.2004.029157. Epub 2004 Nov 11. Ann Rheum Dis. 2005. PMID: 15539411 Free PMC article.

6

Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts.

Hüffmeier U, Traupe H, Burkhardt H, Schürmeier-Horst F, Lascorz J, Böhm B, Lohmann J, Ständer M, Wendler J, Kelsch R, Baumann C, Küster W, Wienker TF, Reis A. Hüffmeier U, et al. J Invest Dermatol. 2005 Jan;124(1):107-10. doi: 10.1111/j.0022-202X.2004.23571.x. J Invest Dermatol. 2005. PMID: 15654961 Free article.

7

Novel autosomal recessive progressive hyperpigmentation syndrome.

Hüffmeier U, Hausser I, Reis A, Rauch A. Hüffmeier U, et al. Am J Med Genet A. 2005 Jun 1;135(2):195-9. doi: 10.1002/ajmg.a.30668. Am J Med Genet A. 2005. PMID: 15852476

8

Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgaris.

Hüffmeier U, Lascorz J, Traupe H, Böhm B, Schürmeier-Horst F, Ständer M, Kelsch R, Baumann C, Küster W, Burkhardt H, Reis A. Hüffmeier U, et al. J Invest Dermatol. 2005 Nov;125(5):906-12. doi: 10.1111/j.0022-202X.2005.23847.x. J Invest Dermatol. 2005. PMID: 16297188 Free article.

9

Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients.

Hüffmeier U, Steffens M, Burkhardt H, Lascorz J, Schürmeier-Horst F, Ständer M, Kelsch R, Baumann C, Küster W, Mössner R, Reich K, Wienker TF, Traupe H, Reis A. Hüffmeier U, et al. J Med Genet. 2006 Jun;43(6):517-22. doi: 10.1136/jmg.2005.037515. Epub 2005 Dec 9. J Med Genet. 2006. PMID: 16339849 Free PMC article.

10

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

Rauch A, Hoyer J, Guth S, Zweier C, Kraus C, Becker C, Zenker M, Hüffmeier U, Thiel C, Rüschendorf F, Nürnberg P, Reis A, Trautmann U. Rauch A, et al. Among authors: huffmeier u. Am J Med Genet A. 2006 Oct 1;140(19):2063-74. doi: 10.1002/ajmg.a.31416. Am J Med Genet A. 2006. PMID: 16917849

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