Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 130

1.

Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder.

Ancín I, Cabranes JA, Vázquez-Álvarez B, Santos JL, Sánchez-Morla E, García-Jiménez MÁ, Fernández C, Barabash A.

World J Biol Psychiatry. 2011 Aug;12(5):376-84. doi: 10.3109/15622975.2011.552192. Epub 2011 May 19.

PMID:
21595525
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. doi: 10.1097/YIC.0b013e328338b884.

PMID:
20531207
3.

COMT polymorphisms as predictors of cognitive dysfunction during manic and mixed episodes in bipolar I disorder.

Soeiro-de-Souza MG, Machado-Vieira R, Soares Bio D, Do Prado CM, Moreno RA.

Bipolar Disord. 2012 Aug;14(5):554-64. doi: 10.1111/j.1399-5618.2012.01030.x. Epub 2012 Jun 19.

PMID:
22713126
4.

COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.

Burdick KE, Funke B, Goldberg JF, Bates JA, Jaeger J, Kucherlapati R, Malhotra AK.

Bipolar Disord. 2007 Jun;9(4):370-6.

PMID:
17547583
5.

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. doi: 10.1016/j.psychres.2013.03.027. Epub 2013 Apr 15.

PMID:
23598060
6.

The COMT and DRD3 genes interacted in bipolar I but not bipolar II disorder.

Lee SY, Chen SL, Chen SH, Huang SY, Tzeng NS, Chang YH, Wang CL, Lee IH, Yeh TL, Yang YK, Lu RB.

World J Biol Psychiatry. 2011 Aug;12(5):385-91. doi: 10.3109/15622975.2010.505298. Epub 2010 Aug 10.

PMID:
20698735
7.

Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.

Zarchi O, Carmel M, Avni C, Attias J, Frisch A, Michaelovsky E, Patya M, Green T, Weinberger R, Weizman A, Gothelf D.

J Psychiatr Res. 2013 Nov;47(11):1623-9. doi: 10.1016/j.jpsychires.2013.07.004. Epub 2013 Aug 1.

PMID:
23910792
8.

COMT Val108/158Met genotype modulates human sensory gating.

Majic T, Rentzsch J, Gudlowski Y, Ehrlich S, Juckel G, Sander T, Lang UE, Winterer G, Gallinat J.

Neuroimage. 2011 Mar 15;55(2):818-24. doi: 10.1016/j.neuroimage.2010.12.031. Epub 2010 Dec 22.

PMID:
21184832
9.

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.

PMID:
18081002
10.

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
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.

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
13.

Association of the G1947A COMT (Val(108/158)Met) gene polymorphism with prefrontal P300 during information processing.

Gallinat J, Bajbouj M, Sander T, Schlattmann P, Xu K, Ferro EF, Goldman D, Winterer G.

Biol Psychiatry. 2003 Jul 1;54(1):40-8.

PMID:
12842307
14.
15.

Recurrence of bipolar mania is associated with catechol-O-methyltransferase Val(108/158)Met polymorphism.

Benedetti F, Dallaspezia S, Locatelli C, Radaelli D, Poletti S, Lorenzi C, Pirovano A, Colombo C, Smeraldi E.

J Affect Disord. 2011 Jul;132(1-2):293-6. doi: 10.1016/j.jad.2011.02.022. Epub 2011 Mar 12.

PMID:
21397335
16.

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. doi: 10.1016/j.psychres.2016.04.029. Epub 2016 Apr 14.

PMID:
27315458
17.

Preliminary evidence of an association between bipolar disorder in females and the catechol-O-methyltransferase gene.

Mynett-Johnson LA, Murphy VE, Claffey E, Shields DC, McKeon P.

Psychiatr Genet. 1998 Winter;8(4):221-5.

PMID:
9861640
18.

Schizotypal dimensions: an intermediate phenotype associated with the COMT high activity allele.

Schürhoff F, Szöke A, Chevalier F, Roy I, Méary A, Bellivier F, Giros B, Leboyer M.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):64-8.

PMID:
17034018
19.

A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population.

Ma X, Sun J, Yao J, Wang Q, Hu X, Deng W, Sun X, Liu X, Murray RM, Collier DA, Li T.

Psychiatry Res. 2007 Sep 30;153(1):7-15. Epub 2007 Jun 29.

PMID:
17604122
20.

COMT and age at onset in mood disorders: a replication and extension study.

Massat I, Kocabas NA, Crisafulli C, Chiesa A, Calati R, Linotte S, Kasper S, Fink M, Antonijevic I, Forray C, Snyder L, Bollen J, Zohar J, De Ronchi D, Souery D, Serretti A, Mendlewicz J.

Neurosci Lett. 2011 Jul 12;498(3):218-21. doi: 10.1016/j.neulet.2011.05.012. Epub 2011 May 11.

PMID:
21600957

Supplemental Content

Support Center