Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia
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Published:2014-07-06
Issue:8
Volume:46
Page:901-904
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Gockel Ines, Becker Jessica, Wouters Mira M, Niebisch Stefan, Gockel Henning R, Hess Timo, Ramonet David, Zimmermann Julian, Vigo Ana González, Trynka Gosia, de León Antonio Ruiz, de la Serna Julio Pérez, Urcelay Elena, Kumar Vinod, Franke Lude, Westra Harm-JanORCID, Drescher Daniel, Kneist Werner, Marquardt Jens U, Galle Peter R, Mattheisen ManuelORCID, Annese Vito, Latiano Anna, Fumagalli Uberto, Laghi Luigi, Cuomo Rosario, Sarnelli Giovanni, Müller Michaela, Eckardt Alexander J, Tack Jan, Hoffmann PerORCID, Herms Stefan, Mangold Elisabeth, Heilmann Stefanie, Kiesslich Ralf, von Rahden Burkhard H A, Allescher Hans-Dieter, Schulz Henning G, Wijmenga Cisca, Heneka Michael T, Lang Hauke, Hopfner Karl-Peter, Nöthen Markus M, Boeckxstaens Guy E, de Bakker Paul I WORCID, Knapp Michael, Schumacher Johannes
Publisher
Springer Science and Business Media LLC
Reference17 articles.
1. Gockel, H.R. et al. Achalasia: will genetic studies provide insights? Hum. Genet. 128, 353–364 (2010). 2. Park, W. & Vaezi, M.F. Etiology and pathogenesis of achalasia: the current understanding. Am. J. Gastroenterol. 100, 1404–1414 (2005). 3. de Bakker, P.I. et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nat. Genet. 38, 1166–1172 (2006). 4. Jia, X. et al. Imputing amino acid polymorphisms in human leukocyte antigens. PLoS ONE 8, e64683 (2013). 5. Senju, S. et al. Allele-specific expression of the cytoplasmic exon of HLA-DQB1 gene. Immunogenetics 36, 319–325 (1992).
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