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Genetic risk for schizophrenia impacts Theory-of-Mind-related brain activation.
Walter H, Schnell K, Erk S, Arnold C, Kirsch P, Esslinger C, Mier D, Schmitgen MM, Rietschel M, Witt SH, Noethen MM, Cichon S, Meyer-Lindenberg A. Walter H, et al. Among authors: witt sh. Mol Psychiatry. 2011 Apr;16(4):353. doi: 10.1038/mp.2011.25. Mol Psychiatry. 2011. PMID: 21430673 No abstract available.
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.
Erk S, Mohnke S, Ripke S, Lett TA, Veer IM, Wackerhagen C, Grimm O, Romanczuk-Seiferth N, Degenhardt F, Tost H, Mattheisen M, Mühleisen TW, Charlet K, Skarabis N, Kiefer F, Cichon S, Witt SH, Nöthen MM, Rietschel M, Heinz A, Meyer-Lindenberg A, Walter H. Erk S, et al. Among authors: witt sh. Transl Psychiatry. 2017 Jan 10;7(1):e997. doi: 10.1038/tp.2016.272. Transl Psychiatry. 2017. PMID: 28072415 Free PMC article.
Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding.
Schott BH, Assmann A, Schmierer P, Soch J, Erk S, Garbusow M, Mohnke S, Pöhland L, Romanczuk-Seiferth N, Barman A, Wüstenberg T, Haddad L, Grimm O, Witt S, Richter S, Klein M, Schütze H, Mühleisen TW, Cichon S, Rietschel M, Noethen MM, Tost H, Gundelfinger ED, Düzel E, Heinz A, Meyer-Lindenberg A, Seidenbecher CI, Walter H. Schott BH, et al. Transl Psychiatry. 2014 Mar 18;4(3):e372. doi: 10.1038/tp.2014.10. Transl Psychiatry. 2014. PMID: 24643163 Free PMC article.
Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.
Degenhardt F, Priebe L, Meier S, Lennertz L, Streit F, Witt SH, Hofmann A, Becker T, Mössner R, Maier W, Nenadic I, Sauer H, Mattheisen M, Buizer-Voskamp J, Ophoff RA; GROUP Consortium; Rujescu D, Giegling I, Ingason A, Wagner M, Delobel B, Andrieux J, Meyer-Lindenberg A, Heinz A, Walter H, Moebus S, Corvin A; Wellcome Trust Case Control Consortium 2, International Schizophrenia Consortium; Rietschel M, Nöthen MM, Cichon S. Degenhardt F, et al. Among authors: witt sh. Transl Psychiatry. 2013 Nov 26;3(11):e326. doi: 10.1038/tp.2013.101. Transl Psychiatry. 2013. PMID: 26151896 Free PMC article.
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nöthen MM, Cichon S, Mühleisen TW. Priebe L, et al. Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1. Mol Psychiatry. 2012. PMID: 21358712
The CACNA1C risk variant for bipolar disorder influences limbic activity.
Wessa M, Linke J, Witt SH, Nieratschker V, Esslinger C, Kirsch P, Grimm O, Hennerici MG, Gass A, King AV, Rietschel M. Wessa M, et al. Among authors: witt sh. Mol Psychiatry. 2010 Dec;15(12):1126-7. doi: 10.1038/mp.2009.103. Epub 2010 Mar 30. Mol Psychiatry. 2010. PMID: 20351721 No abstract available.
296 results