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The serotonin receptor 3E variant is a risk factor for female IBS-D.
Fritz N, Berens S, Dong Y, Martínez C, Schmitteckert S, Houghton LA, Goebel-Stengel M, Wahl V, Kabisch M, Götze D, D'Amato M, Zheng T, Röth R, Mönnikes H, Tesarz J, Engel F, Gauss A, Raithel M, Andresen V, Keller J, Frieling T, Pehl C, Stein-Thöringer C, Clarke G, Kennedy PJ, Cryan JF, Dinan TG, Quigley EMM, Spiller R, Beltrán C, Madrid AM, Torres V, Mayer EA, Sayuk G, Gazouli M, Karamanolis G, Bustamante M, Estivil X, Rabionet R, Hoffmann P, Nöthen MM, Heilmann-Heimbach S, Schmidt B, Franke A, Lieb W, Herzog W, Boeckxstaens G, Wouters MM, Simrén M, Rappold GA, Vicario M, Santos J, Schaefert R, Lorenzo-Bermejo J, Niesler B. Fritz N, et al. Among authors: nothen mm. J Mol Med (Berl). 2022 Nov;100(11):1617-1627. doi: 10.1007/s00109-022-02244-w. Epub 2022 Sep 19. J Mol Med (Berl). 2022. PMID: 36121467 Free PMC article.
Genetics of dyslexia: the evolving landscape.
Schumacher J, Hoffmann P, Schmäl C, Schulte-Körne G, Nöthen MM. Schumacher J, et al. Among authors: nothen mm. J Med Genet. 2007 May;44(5):289-97. doi: 10.1136/jmg.2006.046516. Epub 2007 Feb 16. J Med Genet. 2007. PMID: 17307837 Free PMC article. Review.
Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study.
Hammer C, Cichon S, Mühleisen TW, Haenisch B, Degenhardt F, Mattheisen M, Breuer R, Witt SH, Strohmaier J, Oruc L, Rivas F, Babadjanova G, Grigoroiu-Serbanescu M, Hauser J, Röth R, Rappold G, Rietschel M, Nöthen MM, Niesler B. Hammer C, et al. Among authors: nothen mm. Transl Psychiatry. 2012 Apr 17;2(4):e103. doi: 10.1038/tp.2012.30. Transl Psychiatry. 2012. PMID: 22832903 Free PMC article.
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: nothen mm. Gut. 2014 Sep;63(9):1401-9. doi: 10.1136/gutjnl-2013-304848. Epub 2013 Nov 20. Gut. 2014. PMID: 24259423
A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.
Hammer C, Degenhardt F, Priebe L, Stütz AM, Heilmann S, Waszak SM, Schlattl A, Mangold E, Hoffmann P, Nöthen MM, Rietschel M, Rappold G, Korbel J, Cichon S, Niesler B; MooDS Consortium. Hammer C, et al. Among authors: nothen mm. Bipolar Disord. 2014 Nov;16(7):764-8. doi: 10.1111/bdi.12207. Epub 2014 Apr 23. Bipolar Disord. 2014. PMID: 24754353
Rare SHANK2 variants in schizophrenia.
Peykov S, Berkel S, Degenhardt F, Rietschel M, Nöthen MM, Rappold GA. Peykov S, et al. Among authors: nothen mm. Mol Psychiatry. 2015 Dec;20(12):1487-8. doi: 10.1038/mp.2015.122. Epub 2015 Aug 25. Mol Psychiatry. 2015. PMID: 26303658 Free PMC article. No abstract available.
1,027 results