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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. Transl Psychiatry. 2013 Nov 26;3(11):e326. doi: 10.1038/tp.2013.101. Transl Psychiatry. 2013. PMID: 26151896 Free PMC article.
Neural mechanisms of a genome-wide supported psychosis variant.
Esslinger C, Walter H, Kirsch P, Erk S, Schnell K, Arnold C, Haddad L, Mier D, Opitz von Boberfeld C, Raab K, Witt SH, Rietschel M, Cichon S, Meyer-Lindenberg A. Esslinger C, et al. Science. 2009 May 1;324(5927):605. doi: 10.1126/science.1167768. Science. 2009. PMID: 19407193
A primate-specific, brain isoform of KCNH2 affects cortical physiology, cognition, neuronal repolarization and risk of schizophrenia.
Huffaker SJ, Chen J, Nicodemus KK, Sambataro F, Yang F, Mattay V, Lipska BK, Hyde TM, Song J, Rujescu D, Giegling I, Mayilyan K, Proust MJ, Soghoyan A, Caforio G, Callicott JH, Bertolino A, Meyer-Lindenberg A, Chang J, Ji Y, Egan MF, Goldberg TE, Kleinman JE, Lu B, Weinberger DR. Huffaker SJ, et al. Nat Med. 2009 May;15(5):509-18. doi: 10.1038/nm.1962. Epub 2009 May 3. Nat Med. 2009. PMID: 19412172 Free PMC article.
Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.
Rietschel M, Mattheisen M, Frank J, Treutlein J, Degenhardt F, Breuer R, Steffens M, Mier D, Esslinger C, Walter H, Kirsch P, Erk S, Schnell K, Herms S, Wichmann HE, Schreiber S, Jöckel KH, Strohmaier J, Roeske D, Haenisch B, Gross M, Hoefels S, Lucae S, Binder EB, Wienker TF, Schulze TG, Schmäl C, Zimmer A, Juraeva D, Brors B, Bettecken T, Meyer-Lindenberg A, Müller-Myhsok B, Maier W, Nöthen MM, Cichon S. Rietschel M, et al. Biol Psychiatry. 2010 Sep 15;68(6):578-85. doi: 10.1016/j.biopsych.2010.05.038. Epub 2010 Jul 31. Biol Psychiatry. 2010. PMID: 20673876
Brain function in carriers of a genome-wide supported bipolar disorder variant.
Erk S, Meyer-Lindenberg A, Schnell K, Opitz von Boberfeld C, Esslinger C, Kirsch P, Grimm O, Arnold C, Haddad L, Witt SH, Cichon S, Nöthen MM, Rietschel M, Walter H. Erk S, et al. Arch Gen Psychiatry. 2010 Aug;67(8):803-11. doi: 10.1001/archgenpsychiatry.2010.94. Arch Gen Psychiatry. 2010. PMID: 20679588
Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome.
Feyder M, Karlsson RM, Mathur P, Lyman M, Bock R, Momenan R, Munasinghe J, Scattoni ML, Ihne J, Camp M, Graybeal C, Strathdee D, Begg A, Alvarez VA, Kirsch P, Rietschel M, Cichon S, Walter H, Meyer-Lindenberg A, Grant SG, Holmes A. Feyder M, et al. Am J Psychiatry. 2010 Dec;167(12):1508-17. doi: 10.1176/appi.ajp.2010.10040484. Epub 2010 Oct 15. Am J Psychiatry. 2010. PMID: 20952458 Free PMC article.
760 results