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[Current diagnosis and therapy of achalasia].
Gockel I, Niebisch S, Becker J, Schumacher J, Müller M. Gockel I, et al. Among authors: schumacher j. MMW Fortschr Med. 2016 Dec;158(21-22):80-83. doi: 10.1007/s15006-016-9110-3. MMW Fortschr Med. 2016. PMID: 27966122 Review. German. No abstract available.
Achalasia: will genetic studies provide insights?
Gockel HR, Schumacher J, Gockel I, Lang H, Haaf T, Nöthen MM. Gockel HR, et al. Among authors: schumacher j. Hum Genet. 2010 Oct;128(4):353-64. doi: 10.1007/s00439-010-0874-8. Epub 2010 Aug 11. Hum Genet. 2010. PMID: 20700745 Review.
Etiopathological aspects of achalasia: lessons learned with Hirschsprung's disease.
Gockel HR, Gockel I, Schimanski CC, Schier F, Schumacher J, Nöthen MM, Lang H, Müller M, Eckardt AJ, Eckardt VF. Gockel HR, et al. Among authors: schumacher j. Dis Esophagus. 2012 Aug;25(6):566-72. doi: 10.1111/j.1442-2050.2011.01277.x. Epub 2011 Nov 2. Dis Esophagus. 2012. PMID: 22050474 Review.
Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia.
Wouters MM, Lambrechts D, Becker J, Cleynen I, Tack J, Vigo AG, Ruiz de León A, Urcelay E, Pérez de la Serna J, Rohof W, Annese V, Latiano A, Palmieri O, Mattheisen M, Mueller M, Lang H, Fumagalli U, Laghi L, Zaninotto G, Cuomo R, Sarnelli G, Nöthen MM, Vermeire S, Knapp M, Gockel I, Schumacher J, Boeckxstaens GE. Wouters MM, et al. Among authors: schumacher j. Gut. 2014 Sep;63(9):1401-9. doi: 10.1136/gutjnl-2013-304848. Epub 2013 Nov 20. Gut. 2014. PMID: 24259423
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.
Gockel I, Becker J, Wouters MM, Niebisch S, Gockel HR, Hess T, Ramonet D, Zimmermann J, Vigo AG, Trynka G, de León AR, de la Serna JP, Urcelay E, Kumar V, Franke L, Westra HJ, Drescher D, Kneist W, Marquardt JU, Galle PR, Mattheisen M, Annese V, Latiano A, Fumagalli U, Laghi L, Cuomo R, Sarnelli G, Müller M, Eckardt AJ, Tack J, Hoffmann P, Herms S, Mangold E, Heilmann S, Kiesslich R, von Rahden BH, Allescher HD, Schulz HG, Wijmenga C, Heneka MT, Lang H, Hopfner KP, Nöthen MM, Boeckxstaens GE, de Bakker PI, Knapp M, Schumacher J. Gockel I, et al. Among authors: schumacher j. Nat Genet. 2014 Aug;46(8):901-4. doi: 10.1038/ng.3029. Epub 2014 Jul 6. Nat Genet. 2014. PMID: 24997987
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases.
Lenz TL, Deutsch AJ, Han B, Hu X, Okada Y, Eyre S, Knapp M, Zhernakova A, Huizinga TW, Abecasis G, Becker J, Boeckxstaens GE, Chen WM, Franke A, Gladman DD, Gockel I, Gutierrez-Achury J, Martin J, Nair RP, Nöthen MM, Onengut-Gumuscu S, Rahman P, Rantapää-Dahlqvist S, Stuart PE, Tsoi LC, van Heel DA, Worthington J, Wouters MM, Klareskog L, Elder JT, Gregersen PK, Schumacher J, Rich SS, Wijmenga C, Sunyaev SR, de Bakker PI, Raychaudhuri S. Lenz TL, et al. Among authors: schumacher j. Nat Genet. 2015 Sep;47(9):1085-90. doi: 10.1038/ng.3379. Epub 2015 Aug 10. Nat Genet. 2015. PMID: 26258845 Free PMC article.
1,504 results