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Page 1
Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder.
Amare AT, Thalamuthu A, Schubert KO, Fullerton JM, Ahmed M, Hartmann S, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hou L, Hsu YH, Shekhtman T, Adli M, Akula N, Akiyama K, Ardau R, Arias B, Aubry JM, Hasler R, Richard-Lepouriel H, Perroud N, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka JM, Birner A, Marie-Claire C, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Del Zompo M, DePaulo JR, Étain B, Jamain S, Falkai P, Forstner AJ, Frisen L, Frye MA, Gard S, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Fallgatter AJ, Stegmaier S, Ethofer T, Biere S, Petrova K, Schuster C, Adorjan K, Budde M, Heilbronner M, Kalman JL, Kohshour MO, Reich-Erkelenz D, Schaupp SK, Schulte EC, Senner F, Vogl T, Anghelescu IG, Arolt V, Dannlowski U, Dietrich D, Figge C, Jäger M, Lang FU, Juckel G, Konrad C, Reimer J, Schmauß M, Schmitt A, Spitzer C, von Hagen M, Wiltfang J, Zimmermann J, Andlauer TFM, Fischer A, Bermpohl F, Ritter P, Matura S, Gryaznova A, Falkenberg I, Yildiz C, Kircher T, Schmidt J, Koch M, Gade K, Trost S, Haussleiter IS, Lambert M, Rohenkohl AC, Kraft V, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P,… See abstract for full author list ➔ Amare AT, et al. Among authors: herms s. Mol Psychiatry. 2023 Dec;28(12):5251-5261. doi: 10.1038/s41380-023-02149-1. Epub 2023 Jul 11. Mol Psychiatry. 2023. PMID: 37433967 Free PMC article.
Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
Schirmbeck F, Georgi A, Strohmaier J, Schmael C, Boesshenz KV, Mühleisen TW, Herms S, Hoffmann P, Jamra RA, Schumacher J, Maier W, Propping P, Nöthen MM, Cichon S, Rietschel M, Schulze TG. Schirmbeck F, et al. Among authors: herms s. J Autism Dev Disord. 2008 Nov;38(10):1977-81. doi: 10.1007/s10803-008-0582-6. Epub 2008 May 13. J Autism Dev Disord. 2008. PMID: 18473158
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.
Grigoroiu-Serbanescu M, Herms S, Mühleisen TW, Georgi A, Diaconu CC, Strohmaier J, Czerski P, Hauser J, Leszczynska-Rodziewicz A, Jamra RA, Babadjanova G, Tiganov A, Krasnov V, Kapiletti S, Neagu AI, Vollmer J, Breuer R, Rietschel M, Nöthen MM, Cichon S, Propping P, Nöthen MM, Cichon S. Grigoroiu-Serbanescu M, et al. Among authors: herms s. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1017-21. doi: 10.1002/ajmg.b.30952. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19330776
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
Treutlein J, Mühleisen TW, Frank J, Mattheisen M, Herms S, Ludwig KU, Treutlein T, Schmael C, Strohmaier J, Bösshenz KV, Breuer R, Paul T, Witt SH, Schulze TG, Schlösser RG, Nenadic I, Sauer H, Becker T, Maier W, Cichon S, Nöthen MM, Rietschel M. Treutlein J, et al. Among authors: herms s. Schizophr Res. 2009 Jun;111(1-3):123-30. doi: 10.1016/j.schres.2009.03.011. Epub 2009 Apr 5. Schizophr Res. 2009. PMID: 19346103
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Schumacher J, Laje G, Abou Jamra R, Becker T, Mühleisen TW, Vasilescu C, Mattheisen M, Herms S, Hoffmann P, Hillmer AM, Georgi A, Herold C, Schulze TG, Propping P, Rietschel M, McMahon FJ, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: herms s. Hum Mol Genet. 2009 Jul 15;18(14):2719-27. doi: 10.1093/hmg/ddp204. Epub 2009 May 4. Hum Mol Genet. 2009. PMID: 19414483 Free PMC article.
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent.
Reutter H, Birnbaum S, Mende M, de Assis NA, Hoffmann P, Lacava AD, Herms S, Braumann B, Scheer M, Lauster C, Schmidt G, Schiefke F, Dunsche A, Martini M, Knapp M, Kramer FJ, Nöthen MM, Mangold E. Reutter H, et al. Among authors: herms s. Int J Pediatr Otorhinolaryngol. 2009 Oct;73(10):1334-8. doi: 10.1016/j.ijporl.2009.06.004. Epub 2009 Jul 7. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19586667
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.
Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: herms s. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):503-511. doi: 10.1002/ajmg.b.31007. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19591125
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
Mangold E, Ludwig KU, Birnbaum S, Baluardo C, Ferrian M, Herms S, Reutter H, de Assis NA, Chawa TA, Mattheisen M, Steffens M, Barth S, Kluck N, Paul A, Becker J, Lauster C, Schmidt G, Braumann B, Scheer M, Reich RH, Hemprich A, Pötzsch S, Blaumeiser B, Moebus S, Krawczak M, Schreiber S, Meitinger T, Wichmann HE, Steegers-Theunissen RP, Kramer FJ, Cichon S, Propping P, Wienker TF, Knapp M, Rubini M, Mossey PA, Hoffmann P, Nöthen MM. Mangold E, et al. Among authors: herms s. Nat Genet. 2010 Jan;42(1):24-6. doi: 10.1038/ng.506. Epub 2009 Dec 20. Nat Genet. 2010. PMID: 20023658
228 results