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Items: 1 to 20 of 407

1.
2.

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;60(9):889-96.

PMID:
12963670
3.

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. doi: 10.1177/0269881111400644. Epub 2011 Mar 29.

PMID:
21447540
4.

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. Epub 2005 Dec 5.

PMID:
16330500
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. Epub 2007 Apr 7.

PMID:
17482701
6.

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.

Handoko HY, Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ.

Mol Psychiatry. 2005 Jun;10(6):589-97.

PMID:
15505638
7.

Prefrontal neurons and the genetics of schizophrenia.

Weinberger DR, Egan MF, Bertolino A, Callicott JH, Mattay VS, Lipska BK, Berman KF, Goldberg TE.

Biol Psychiatry. 2001 Dec 1;50(11):825-44. Review.

PMID:
11743939
8.

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;69(3):234-8.

PMID:
16542388
9.
11.

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 7;417(3):271-4. Epub 2007 Mar 2.

PMID:
17383818
12.

Association study of a functional catechol-O-methyltransferase-gene polymorphism and cognitive function in healthy females.

Tsai SJ, Yu YW, Chen TJ, Chen JY, Liou YJ, Chen MC, Hong CJ.

Neurosci Lett. 2003 Feb 27;338(2):123-6.

PMID:
12566168
13.

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.

Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG, Wildenauer DB, Martinez M, Gejman PV.

Mol Psychiatry. 2005 Apr;10(4):353-65.

PMID:
15340358
14.

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. doi: 10.1055/s-0028-1112132. Epub 2009 Jul 7.

PMID:
19585392
15.

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;16(3):117-24.

PMID:
16691129
16.
17.

A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype.

Tunbridge EM, Weinberger DR, Harrison PJ.

Mol Psychiatry. 2006 Feb;11(2):116-7. No abstract available.

PMID:
16247488
18.

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté A, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Yakir B, Zak NB, Darvasi A.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):61-4.

PMID:
15211633
19.

Sexually dimorphic interaction between the DRD1 and COMT genes in schizophrenia.

Hoenicka J, Garrido E, Ponce G, Rodríguez-Jiménez R, Martínez I, Rubio G, Jiménez-Arriero MA, Palomo T.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):948-54. doi: 10.1002/ajmg.b.31065.

PMID:
20127886
20.

Family-based and case-control study of catechol-O-methyltransferase in schizophrenia among Palestinian Arabs.

Kremer I, Pinto M, Murad I, Muhaheed M, Bannoura I, Muller DJ, Schulze TG, Reshef A, Blanaru M, Gathas S, Goichman R, Rietschel M, Dobrusin M, Bachner-Melman R, Nemanov L, Belmaker RH, Maier W, Ebstein RP.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):35-9.

PMID:
12707935

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