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Items: 1 to 20 of 382

1.

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.

PMID:
15124004
2.

Association of the 3' region of COMT with schizophrenia in Taiwan.

Chien YL, Liu CM, Fann CS, Liu YL, Hwu HG.

J Formos Med Assoc. 2009 Apr;108(4):301-9. doi: 10.1016/S0929-6646(09)60070-X.

3.

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
4.
5.

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. doi: 10.1097/YIC.0b013e328338b884.

PMID:
20531207
6.

Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.

Nicodemus KK, Kolachana BS, Vakkalanka R, Straub RE, Giegling I, Egan MF, Rujescu D, Weinberger DR.

Hum Genet. 2007 Feb;120(6):889-906. Epub 2006 Sep 28.

PMID:
17006672
7.

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.

PMID:
16027741
8.

Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.

Borroni B, Grassi M, Costanzi C, Zanetti M, Archetti S, Franzoni S, Caimi L, Padovani A.

Neurobiol Aging. 2007 Aug;28(8):1231-8. Epub 2006 Jul 11.

PMID:
16837108
9.

A highly significant association between a COMT haplotype and schizophrenia.

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

Am J Hum Genet. 2002 Dec;71(6):1296-302. Epub 2002 Oct 25.

10.

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
11.

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
12.

Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control study.

Yu R, Zhang XN, Huang XX, Ding SP, Li JC.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):570-3.

PMID:
17427186
13.

COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

Palmatier MA, Pakstis AJ, Speed W, Paschou P, Goldman D, Odunsi A, Okonofua F, Kajuna S, Karoma N, Kungulilo S, Grigorenko E, Zhukova OV, Bonne-Tamir B, Lu RB, Parnas J, Kidd JR, DeMille MM, Kidd KK.

Mol Psychiatry. 2004 Sep;9(9):859-70.

PMID:
15098000
14.

Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.

Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):45-50.

PMID:
16118784
15.

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

Chen J, Lipska BK, Halim N, Ma QD, Matsumoto M, Melhem S, Kolachana BS, Hyde TM, Herman MM, Apud J, Egan MF, Kleinman JE, Weinberger DR.

Am J Hum Genet. 2004 Nov;75(5):807-21. Epub 2004 Sep 27. Erratum in: Am J Hum Genet. 2005 Jun;76(6):1089.

16.

Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.

Halleland H, Lundervold AJ, Halmøy A, Haavik J, Johansson S.

Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):403-10. doi: 10.1002/ajmg.b.30831.

PMID:
18802928
17.

No evidence for linkage between COMT and schizophrenia in a French population.

de Chaldée M, Corbex M, Campion D, Jay M, Samolyk D, Petit M, Thibaut F, Laurent C, Mallet J.

Psychiatry Res. 2001 May 10;102(1):87-90.

PMID:
11368843
18.

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families.

Kunugi H, Vallada HP, Sham PC, Hoda F, Arranz MJ, Li T, Nanko S, Murray RM, McGuffin P, Owen M, Gill M, Collier DA.

Psychiatr Genet. 1997 Autumn;7(3):97-101.

PMID:
9323320
19.

Regulator of G-protein signaling 4 (RGS4) gene is associated with schizophrenia in Irish high density families.

Chen X, Dunham C, Kendler S, Wang X, O'Neill FA, Walsh D, Kendler KS.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):23-6.

PMID:
15274033
20.

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. Epub 2007 May 14.

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