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Journal Abstract Search

486 related items for PubMed ID: 19585392

  • 1. COMT Val 158 Met polymorphism is associated with cognitive flexibility in a signal discrimination task in schizophrenia.
    Neuhaus AH, Opgen-Rhein C, Urbanek C, Hahn E, Ta TM, Seidelsohn M, Strathmann S, Kley F, Wieseke N, Sander T, Dettling M.
    Pharmacopsychiatry; 2009 Jul; 42(4):141-4. PubMed ID: 19585392
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  • 3. Influence of catechol-O-methyltransferase Val158Met polymorphism on neuropsychological and functional outcomes of classical rehabilitation and cognitive remediation in schizophrenia.
    Bosia M, Bechi M, Marino E, Anselmetti S, Poletti S, Cocchi F, Smeraldi E, Cavallaro R.
    Neurosci Lett; 2007 May 07; 417(3):271-4. PubMed ID: 17383818
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  • 4. Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.
    Goldberg TE, Egan MF, Gscheidle T, Coppola R, Weickert T, Kolachana BS, Goldman D, Weinberger DR.
    Arch Gen Psychiatry; 2003 Sep 07; 60(9):889-96. PubMed ID: 12963670
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  • 6. Effect of schizotypy on cognitive performance and its tuning by COMT val158 met genotype variations in a large population of young men.
    Smyrnis N, Avramopoulos D, Evdokimidis I, Stefanis CN, Tsekou H, Stefanis NC.
    Biol Psychiatry; 2007 Apr 01; 61(7):845-53. PubMed ID: 17123481
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  • 7. Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary results.
    Zinkstok J, van Nimwegen L, van Amelsvoort T, de Haan L, Yusuf MA, Baas F, Linszen D.
    Psychiatry Res; 2008 Jan 15; 157(1-3):1-8. PubMed ID: 17850881
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  • 8. Association study of COMT gene Val158Met polymorphism with auditory P300 and performance on neurocognitive tests in patients with schizophrenia and their relatives.
    Golimbet V, Gritsenko I, Alfimova M, Lebedeva I, Lezheiko T, Abramova L, Kaleda V, Ebstein R.
    World J Biol Psychiatry; 2006 Jan 15; 7(4):238-45. PubMed ID: 17071544
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  • 9. The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.
    Ohnishi T, Hashimoto R, Mori T, Nemoto K, Moriguchi Y, Iida H, Noguchi H, Nakabayashi T, Hori H, Ohmori M, Tsukue R, Anami K, Hirabayashi N, Harada S, Arima K, Saitoh O, Kunugi H.
    Brain; 2006 Feb 15; 129(Pt 2):399-410. PubMed ID: 16330500
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  • 10. The flexible mind is associated with the catechol-O-methyltransferase (COMT) Val158Met polymorphism: evidence for a role of dopamine in the control of task-switching.
    Colzato LS, Waszak F, Nieuwenhuis S, Posthuma D, Hommel B.
    Neuropsychologia; 2010 Jul 15; 48(9):2764-8. PubMed ID: 20434465
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  • 11. Effects of brain-derived neurotrophic factor-catecholamine-O-methyltransferase gene interaction on schizophrenic symptoms.
    Han DH, Park DB, Choi TY, Joo SY, Lee MK, Park BR, Nishimura R, Chu CC, Renshaw PF.
    Neuroreport; 2008 Jul 16; 19(11):1155-8. PubMed ID: 18596619
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  • 12. Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
    Shashi V, Keshavan MS, Howard TD, Berry MN, Basehore MJ, Lewandowski E, Kwapil TR.
    Clin Genet; 2006 Mar 16; 69(3):234-8. PubMed ID: 16542388
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  • 13. COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.
    Burdick KE, Funke B, Goldberg JF, Bates JA, Jaeger J, Kucherlapati R, Malhotra AK.
    Bipolar Disord; 2007 Jun 16; 9(4):370-6. PubMed ID: 17547583
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  • 14. The catechol O-methyltransferase Val158Met polymorphism and herpes simplex virus type 1 infection are risk factors for cognitive impairment in bipolar disorder: additive gene-environmental effects in a complex human psychiatric disorder.
    Dickerson FB, Boronow JJ, Stallings C, Origoni AE, Cole S, Leister F, Krivogorsky B, Yolken RH.
    Bipolar Disord; 2006 Apr 16; 8(2):124-32. PubMed ID: 16542182
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  • 15. Prefrontal electrophysiologic "noise" and catechol-O-methyltransferase genotype in schizophrenia.
    Winterer G, Egan MF, Kolachana BS, Goldberg TE, Coppola R, Weinberger DR.
    Biol Psychiatry; 2006 Sep 15; 60(6):578-84. PubMed ID: 16730334
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  • 16. Catechol-O-methyltransferase (COMT) genotype moderates the effects of childhood trauma on cognition and symptoms in schizophrenia.
    Green MJ, Chia TY, Cairns MJ, Wu J, Tooney PA, Scott RJ, Carr VJ, Australian Schizophrenia Research Bank.
    J Psychiatr Res; 2014 Feb 15; 49():43-50. PubMed ID: 24252819
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  • 17. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia.
    Haraldsson HM, Ettinger U, Magnusdottir BB, Sigmundsson T, Sigurdsson E, Ingason A, Petursson H.
    Psychiatry Res; 2009 Sep 30; 169(2):173-5. PubMed ID: 19647329
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  • 18. Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia.
    Liao SY, Lin SH, Liu CM, Hsieh MH, Hwang TJ, Liu SK, Guo SC, Hwu HG, Chen WJ.
    Genes Brain Behav; 2009 Mar 30; 8(2):228-37. PubMed ID: 19077118
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  • 19. COMT val158Met and executive control: a test of the benefit of specific deficits to translational research.
    MacDonald AW, Carter CS, Flory JD, Ferrell RE, Manuck SB.
    J Abnorm Psychol; 2007 May 30; 116(2):306-12. PubMed ID: 17516763
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  • 20. COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.
    Baker K, Baldeweg T, Sivagnanasundaram S, Scambler P, Skuse D.
    Biol Psychiatry; 2005 Jul 01; 58(1):23-31. PubMed ID: 15935994
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