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A myelin gene causative of a catatonia-depression syndrome upon aging.
Hagemeyer N, Goebbels S, Papiol S, Kästner A, Hofer S, Begemann M, Gerwig UC, Boretius S, Wieser GL, Ronnenberg A, Gurvich A, Heckers SH, Frahm J, Nave KA, Ehrenreich H. Hagemeyer N, et al. Among authors: kastner a. EMBO Mol Med. 2012 Jun;4(6):528-39. doi: 10.1002/emmm.201200230. Epub 2012 Apr 4. EMBO Mol Med. 2012. PMID: 22473874 Free PMC article.
Common variants of the genes encoding erythropoietin and its receptor modulate cognitive performance in schizophrenia.
Kästner A, Grube S, El-Kordi A, Stepniak B, Friedrichs H, Sargin D, Schwitulla J, Begemann M, Giegling I, Miskowiak KW, Sperling S, Hannke K, Ramin A, Heinrich R, Gefeller O, Nave KA, Rujescu D, Ehrenreich H. Kästner A, et al. Mol Med. 2012 Sep 7;18(1):1029-40. doi: 10.2119/molmed.2012.00190. Mol Med. 2012. PMID: 22669473 Free PMC article.
Mild expression differences of MECP2 influencing aggressive social behavior.
Tantra M, Hammer C, Kästner A, Dahm L, Begemann M, Bodda C, Hammerschmidt K, Giegling I, Stepniak B, Castillo Venzor A, Konte B, Erbaba B, Hartmann A, Tarami A, Schulz-Schaeffer W, Rujescu D, Mannan AU, Ehrenreich H. Tantra M, et al. Among authors: kastner a. EMBO Mol Med. 2014 May;6(5):662-84. doi: 10.1002/emmm.201303744. EMBO Mol Med. 2014. PMID: 24648499 Free PMC article.
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.
Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, Fischer U, Dityatev A, Grabe HJ, Rujescu D, Fischer A, Ehrenreich H. Stepniak B, et al. Among authors: kastner a. EMBO Mol Med. 2015 Dec;7(12):1565-79. doi: 10.15252/emmm.201505696. EMBO Mol Med. 2015. PMID: 26612855 Free PMC article.
The cross-sectional GRAS sample: a comprehensive phenotypical data collection of schizophrenic patients.
Ribbe K, Friedrichs H, Begemann M, Grube S, Papiol S, Kästner A, Gerchen MF, Ackermann V, Tarami A, Treitz A, Flögel M, Adler L, Aldenhoff JB, Becker-Emner M, Becker T, Czernik A, Dose M, Folkerts H, Freese R, Günther R, Herpertz S, Hesse D, Kruse G, Kunze H, Franz M, Löhrer F, Maier W, Mielke A, Müller-Isberner R, Oestereich C, Pajonk FG, Pollmächer T, Schneider U, Schwarz HJ, Kröner-Herwig B, Havemann-Reinecke U, Frahm J, Stühmer W, Falkai P, Brose N, Nave KA, Ehrenreich H. Ribbe K, et al. Among authors: kastner a. BMC Psychiatry. 2010 Nov 10;10:91. doi: 10.1186/1471-244X-10-91. BMC Psychiatry. 2010. PMID: 21067598 Free PMC article.
Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.
El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H. El-Kordi A, et al. Among authors: kastner a. Behav Brain Res. 2013 Aug 15;251:41-9. doi: 10.1016/j.bbr.2012.11.016. Epub 2012 Nov 23. Behav Brain Res. 2013. PMID: 23183221
A single gene defect causing claustrophobia.
El-Kordi A, Kästner A, Grube S, Klugmann M, Begemann M, Sperling S, Hammerschmidt K, Hammer C, Stepniak B, Patzig J, de Monasterio-Schrader P, Strenzke N, Flügge G, Werner HB, Pawlak R, Nave KA, Ehrenreich H. El-Kordi A, et al. Among authors: kastner a. Transl Psychiatry. 2013 Apr 30;3(4):e254. doi: 10.1038/tp.2013.28. Transl Psychiatry. 2013. PMID: 23632458 Free PMC article.
162 results