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Journal Abstract Search

134 related items for PubMed ID: 21595525

  • 21. Association between hypnotizability and the catechol-O-methyltransferase (COMT) polymorphism.
    Szekely A, Kovacs-Nagy R, Bányai EI, Gosi-Greguss AC, Varga K, Halmai Z, Ronai Z, Sasvari-Szekely M.
    Int J Clin Exp Hypn; 2010 Jul; 58(3):301-15. PubMed ID: 20509070
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  • 22. Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk.
    Gellekink H, Muntjewerff JW, Vermeulen SH, Hermus AR, Blom HJ, den Heijer M.
    Thromb Haemost; 2007 Dec; 98(6):1226-31. PubMed ID: 18064318
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  • 23. Catechol O-methyltransferase and monoamine oxidase A genotypes, and plasma catecholamine metabolites in bipolar and schizophrenic patients.
    Zumárraga M, Dávila R, Basterreche N, Arrue A, Goienetxea B, Zamalloa MI, Erkoreka L, Bustamante S, Inchausti L, González-Torres MA, Guimón J.
    Neurochem Int; 2010 Dec; 56(6-7):774-9. PubMed ID: 20206656
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  • 24. Association of catechol-O-methyltransferase Val(108/158) Met genetic polymorphism with schizophrenia, P50 sensory gating, and negative symptoms in a Chinese population.
    Mao Q, Tan YL, Luo XG, Tian L, Wang ZR, Tan SP, Chen S, Yang GG, An HM, Yang FD, Zhang XY.
    Psychiatry Res; 2016 Aug 30; 242():271-276. PubMed ID: 27315458
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  • 25. Effect of catechol O-methyltransferase val(158)met polymorphism on the p50 gating endophenotype in schizophrenia.
    Lu BY, Martin KE, Edgar JC, Smith AK, Lewis SF, Escamilla MA, Miller GA, Cañive JM.
    Biol Psychiatry; 2007 Oct 01; 62(7):822-5. PubMed ID: 17448448
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  • 26. P50 sensory gating is a trait marker of the bipolar spectrum.
    Cabranes JA, Ancín I, Santos JL, Sánchez-Morla E, García-Jiménez MA, Rodríguez-Moya L, Fernández C, Barabash A.
    Eur Neuropsychopharmacol; 2013 Jul 01; 23(7):721-7. PubMed ID: 22770636
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  • 27. 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 01; 129(Pt 2):399-410. PubMed ID: 16330500
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  • 30. Association between catechol-O-methyltransferase Val(108/158)Met polymorphism and psychotic features of bipolar disorder.
    Benedetti F, Dallaspezia S, Colombo C, Lorenzi C, Pirovano A, Smeraldi E.
    J Affect Disord; 2010 Sep 01; 125(1-3):341-4. PubMed ID: 20122740
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  • 31. Catechol-O-methyltransferase Val158Met genotype variation is associated with prefrontal-dependent task performance in schizotypal personality disorder patients and comparison groups.
    Minzenberg MJ, Xu K, Mitropoulou V, Harvey PD, Finch T, Flory JD, New AS, Goldman D, Siever LJ.
    Psychiatr Genet; 2006 Jun 01; 16(3):117-24. PubMed ID: 16691129
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  • 32. Role of COMT, 5-HT(1A) , and SERT genetic polymorphisms on antidepressant response to Transcranial Magnetic Stimulation.
    Malaguti A, Rossini D, Lucca A, Magri L, Lorenzi C, Pirovano A, Colombo C, Smeraldi E, Zanardi R.
    Depress Anxiety; 2011 Jul 01; 28(7):568-73. PubMed ID: 21449006
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  • 33. CHRNA7 haplotypes are associated with impaired attention in euthymic bipolar disorder.
    Ancín I, Cabranes JA, Santos JL, Sánchez-Morla E, Vázquez-Álvarez B, Rodríguez-Moya L, Pousada-Casal A, Fernández C, Aparicio A, Barabash A.
    J Affect Disord; 2011 Sep 01; 133(1-2):340-5. PubMed ID: 21550667
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  • 37. No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population.
    Van Den Bogaert A, Sleegers K, De Zutter S, Heyrman L, Norrback KF, Adolfsson R, Van Broeckhoven C, Del-Favero J.
    Psychiatr Genet; 2006 Oct 01; 16(5):209-12. PubMed ID: 16969276
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  • 38. How to consistently link extraversion and intelligence to the catechol-O-methyltransferase (COMT) gene: on defining and measuring psychological phenotypes in neurogenetic research.
    Wacker J, Mueller EM, Hennig J, Stemmler G.
    J Pers Soc Psychol; 2012 Feb 01; 102(2):427-44. PubMed ID: 22180998
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  • 39. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype.
    Eisenberg J, Mei-Tal G, Steinberg A, Tartakovsky E, Zohar A, Gritsenko I, Nemanov L, Ebstein RP.
    Am J Med Genet; 1999 Oct 15; 88(5):497-502. PubMed ID: 10490706
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