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Page 1
Association of a functional 1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia.
Rothe C, Gutknecht L, Freitag C, Tauber R, Mössner R, Franke P, Fritze J, Wagner G, Peikert G, Wenda B, Sand P, Jacob C, Rietschel M, Nöthen MM, Garritsen H, Fimmers R, Deckert J, Lesch KP. Rothe C, et al. Among authors: fimmers r. Int J Neuropsychopharmacol. 2004 Jun;7(2):189-92. doi: 10.1017/S1461145703004061. Epub 2004 Feb 25. Int J Neuropsychopharmacol. 2004. PMID: 14984628 Free article.
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
Domschke K, Freitag CM, Kuhlenbäumer G, Schirmacher A, Sand P, Nyhuis P, Jacob C, Fritze J, Franke P, Rietschel M, Garritsen HS, Fimmers R, Nöthen MM, Lesch KP, Stögbauer F, Deckert J. Domschke K, et al. Among authors: fimmers r. Int J Neuropsychopharmacol. 2004 Jun;7(2):183-8. doi: 10.1017/S146114570400416X. Epub 2004 Mar 5. Int J Neuropsychopharmacol. 2004. PMID: 15009906 Free article.
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder.
Lee YJ, Hohoff C, Domschke K, Sand P, Kuhlenbäumer G, Schirmacher A, Freitag CM, Meyer J, Stöber G, Franke P, Nöthen MM, Fritze J, Fimmers R, Garritsen HS, Stögbauer F, Deckert J. Lee YJ, et al. Among authors: fimmers r. Neurosci Lett. 2005 Mar 22;377(1):40-3. doi: 10.1016/j.neulet.2004.11.063. Epub 2004 Dec 15. Neurosci Lett. 2005. PMID: 15722184
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.
Haenisch B, Linsel K, Brüss M, Gilsbach R, Propping P, Nöthen MM, Rietschel M, Fimmers R, Maier W, Zobel A, Höfels S, Guttenthaler V, Göthert M, Bönisch H. Haenisch B, et al. Among authors: fimmers r. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1013-6. doi: 10.1002/ajmg.b.30912. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19105200
Familial occurrence of systemic mast cell activation disease.
Molderings GJ, Haenisch B, Bogdanow M, Fimmers R, Nöthen MM. Molderings GJ, et al. Among authors: fimmers r. PLoS One. 2013 Sep 30;8(9):e76241. doi: 10.1371/journal.pone.0076241. eCollection 2013. PLoS One. 2013. PMID: 24098785 Free PMC article.
Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia.
Becker J, Niebisch S, Ricchiuto A, Schaich EJ, Lehmann G, Waltgenbach T, Schafft A, Hess T, Lenze F, Venerito M, Hüneburg R, Lingohr P, Matthaei H, Seewald S, Scheuermann U, Kreuser N, Veits L, Wouters MM, Gockel HR, Lang H, Vieth M, Müller M, Eckardt AJ, von Rahden BH, Knapp M, Boeckxstaens GE, Fimmers R, Nöthen MM, Schulz HG, Gockel I, Schumacher J. Becker J, et al. Among authors: fimmers r. Eur J Gastroenterol Hepatol. 2016 Jun;28(6):689-95. doi: 10.1097/MEG.0000000000000602. Eur J Gastroenterol Hepatol. 2016. PMID: 26882171
MGMT promoter methylation analysis for allocating combined CCNU/TMZ chemotherapy: Lessons learned from the CeTeG/NOA-09 trial.
Tzaridis T, Schäfer N, Weller J, Steinbach JP, Schlegel U, Seidel S, Sabel M, Hau P, Seidel C, Krex D, Goldbrunner R, Tonn JC, Grauer O, Kebir S, Schneider M, Schaub C, Vatter H, Coch C, Glas M, Fimmers R, Pietsch T, Reifenberger G, Herrlinger U, Felsberg J. Tzaridis T, et al. Among authors: fimmers r. Int J Cancer. 2021 Apr 1;148(7):1695-1707. doi: 10.1002/ijc.33363. Epub 2020 Nov 10. Int J Cancer. 2021. PMID: 33113214 Clinical Trial.
435 results