279 related articles for article (PubMed ID: 16233957)
1. Analysis of an association between the COMT polymorphism and clinical symptomatology in schizophrenia.
Strous RD; Lapidus R; Viglin D; Kotler M; Lachman HM
Neurosci Lett; 2006 Jan; 393(2-3):170-3. PubMed ID: 16233957
[TBL] [Abstract][Full Text] [Related]
2. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women.
Sazci A; Ergul E; Kucukali I; Kilic G; Kaya G; Kara I
Brain Res Mol Brain Res; 2004 Dec; 132(1):51-6. PubMed ID: 15548428
[TBL] [Abstract][Full Text] [Related]
3. Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment.
Molero P; Ortuño F; Zalacain M; Patiño-García A
Pharmacogenomics J; 2007 Dec; 7(6):418-26. PubMed ID: 17363961
[TBL] [Abstract][Full Text] [Related]
4. Association study of a functional catechol-O-methyltransferase genetic polymorphism with age of onset, cognitive function, symptomatology and prognosis in chronic schizophrenia.
Tsai SJ; Hong CJ; Liao DL; Lai IC; Liou YJ
Neuropsychobiology; 2004; 49(4):196-200. PubMed ID: 15118357
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.
Boot E; Booij J; Abeling N; Meijer J; da Silva Alves F; Zinkstok J; Baas F; Linszen D; van Amelsvoort T
J Psychopharmacol; 2011 Jul; 25(7):888-95. PubMed ID: 21447540
[TBL] [Abstract][Full Text] [Related]
7. Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.
Tunbridge E; Burnet PW; Sodhi MS; Harrison PJ
Synapse; 2004 Feb; 51(2):112-8. PubMed ID: 14618678
[TBL] [Abstract][Full Text] [Related]
8. Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia.
Muntjewerff JW; Gellekink H; den Heijer M; Hoogendoorn ML; Kahn RS; Sinke RJ; Blom HJ
Eur Neuropsychopharmacol; 2008 Feb; 18(2):99-106. PubMed ID: 17716874
[TBL] [Abstract][Full Text] [Related]
9. 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
[TBL] [Abstract][Full Text] [Related]
10. 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; 157(1-3):1-8. PubMed ID: 17850881
[TBL] [Abstract][Full Text] [Related]
11. Genetic susceptibility of catechol-O-methyltransferase polymorphism in Japanese patients with breast cancer.
Inoue H; Shibuta K; Matsuyama A; Yoshinaga K; Sadanaga N; Ueo H; Barnard GF; Mori M
Oncol Rep; 2005 Sep; 14(3):707-12. PubMed ID: 16077979
[TBL] [Abstract][Full Text] [Related]
12. Polymorphisms of dopamine degradation enzyme (COMT and MAO) genes and tardive dyskinesia in patients with schizophrenia.
Matsumoto C; Shinkai T; Hori H; Ohmori O; Nakamura J
Psychiatry Res; 2004 Jun; 127(1-2):1-7. PubMed ID: 15261699
[TBL] [Abstract][Full Text] [Related]
13. Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.
Norton N; Kirov G; Zammit S; Jones G; Jones S; Owen R; Krawczak M; Williams NM; O'Donovan MC; Owen MJ
Am J Med Genet; 2002 Jul; 114(5):491-6. PubMed ID: 12116182
[TBL] [Abstract][Full Text] [Related]
14. Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia.
Chen CH; Lee YR; Liu MY; Wei FC; Koong FJ; Hwu HG; Hsiao KJ
Am J Med Genet; 1996 Nov; 67(6):556-9. PubMed ID: 8950414
[TBL] [Abstract][Full Text] [Related]
15. Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder.
Erdal ME; Tot S; Yazici K; Yazici A; Herken H; Erdem P; Derici E; Camdeviren H
Depress Anxiety; 2003; 18(1):41-5. PubMed ID: 12900951
[TBL] [Abstract][Full Text] [Related]
16. 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; 169(2):173-5. PubMed ID: 19647329
[TBL] [Abstract][Full Text] [Related]
17. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
Zinkstok J; Schmitz N; van Amelsvoort T; Moeton M; Baas F; Linszen D
Genes Brain Behav; 2008 Feb; 7(1):61-9. PubMed ID: 17504246
[TBL] [Abstract][Full Text] [Related]
18. 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; 129(Pt 2):399-410. PubMed ID: 16330500
[TBL] [Abstract][Full Text] [Related]
19. COMT gene val158met polymorphism in patients with dyspeptic symptoms.
Tahara T; Arisawa T; Shibata T; Nakamura M; Wang F; Hirata I
Hepatogastroenterology; 2008; 55(84):979-82. PubMed ID: 18705311
[TBL] [Abstract][Full Text] [Related]
20. Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia.
Wang Y; Hu Y; Fang Y; Zhang K; Yang H; Ma J; Xu Q; Shen Y
Biol Psychiatry; 2009 Jun; 65(12):1048-54. PubMed ID: 19159868
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]