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Journal Abstract Search

199 related items for PubMed ID: 18081002

  • 1. Association of catechol-O-methyltransferase variants with loudness dependence of auditory evoked potentials.
    Juckel G, Kawohl W, Giegling I, Mavrogiorgou P, Winter C, Pogarell O, Mulert C, Hegerl U, Rujescu D.
    Hum Psychopharmacol; 2008 Mar; 23(2):115-20. PubMed ID: 18081002
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  • 2. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
    Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I.
    Int Clin Psychopharmacol; 2010 Jul; 25(4):218-27. PubMed ID: 20531207
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  • 3. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.
    Chen X, Wang X, O'Neill AF, Walsh D, Kendler KS.
    Mol Psychiatry; 2004 Oct; 9(10):962-7. PubMed ID: 15124004
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  • 4. Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease.
    Sweet RA, Devlin B, Pollock BG, Sukonick DL, Kastango KB, Bacanu SA, Chowdari KV, DeKosky ST, Ferrell RE.
    Mol Psychiatry; 2005 Nov; 10(11):1026-36. PubMed ID: 16027741
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  • 5. Serotonergic functioning as measured by the loudness dependence of auditory evoked potentials is related to a haplotype in the brain-derived neurotrophic factor (BDNF) gene.
    Juckel G, Schumacher C, Giegling I, Assion HJ, Mavrogiorgou P, Pogarell O, Mulert C, Hegerl U, Norra C, Rujescu D.
    J Psychiatr Res; 2010 Jun; 44(8):541-6. PubMed ID: 20004415
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  • 9. No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.
    Nunokawa A, Watanabe Y, Muratake T, Kaneko N, Koizumi M, Someya T.
    Neurosci Res; 2007 Jul; 58(3):291-6. PubMed ID: 17482701
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  • 11. Association study of polymorphisms in the alpha 7 nicotinic acetylcholine receptor subunit and catechol-o-methyl transferase genes with sensory gating in first-episode schizophrenia.
    Liu X, Hong X, Chan RC, Kong F, Peng Z, Wan X, Wang C, Cheng L.
    Psychiatry Res; 2013 Oct 30; 209(3):431-8. PubMed ID: 23598060
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  • 17. Auditory event-related potentials (P3a, P3b) and genetic variants within the dopamine and serotonin system in healthy females.
    Heitland I, Kenemans JL, Oosting RS, Baas JM, Böcker KB.
    Behav Brain Res; 2013 Jul 15; 249():55-64. PubMed ID: 23619133
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  • 18. Impact of complex genetic variation in COMT on human brain function.
    Meyer-Lindenberg A, Nichols T, Callicott JH, Ding J, Kolachana B, Buckholtz J, Mattay VS, Egan M, Weinberger DR.
    Mol Psychiatry; 2006 Sep 15; 11(9):867-77, 797. PubMed ID: 16786032
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  • 19. DBH -1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task.
    Spronk DB, Veth CP, Arns M, Schofield PR, Dobson-Stone C, Ramaekers JG, Franke B, de Bruijn ER, Verkes RJ.
    Clin Neurophysiol; 2013 May 15; 124(5):909-15. PubMed ID: 23261162
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