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Items: 1 to 20 of 93

1.

Schooling and variation in the COMT gene: the devil is in the details.

Campbell D, Bick J, Yrigollen CM, Lee M, Joseph A, Chang JT, Grigorenko EL; Learning Disabilities Project: Zambia.

J Child Psychol Psychiatry. 2013 Oct;54(10):1056-65. doi: 10.1111/jcpp.12120. Epub 2013 Aug 19.

2.

Haplotypes of catechol-O-methyltransferase modulate intelligence-related brain white matter integrity.

Liu B, Li J, Yu C, Li Y, Liu Y, Song M, Fan M, Li K, Jiang T.

Neuroimage. 2010 Mar;50(1):243-9. doi: 10.1016/j.neuroimage.2009.12.020. Epub 2009 Dec 11.

PMID:
20005296
3.

Effects of catechol-O-methyltransferase on normal variation in the cognitive function of children.

Barnett JH, Heron J, Goldman D, Jones PB, Xu K.

Am J Psychiatry. 2009 Aug;166(8):909-16. doi: 10.1176/appi.ajp.2009.08081251. Epub 2009 Jul 15.

4.

Gene-gene interaction between COMT and MAOA potentially predicts the intelligence of attention-deficit hyperactivity disorder boys in China.

Qian QJ, Yang L, Wang YF, Zhang HB, Guan LL, Chen Y, Ji N, Liu L, Faraone SV.

Behav Genet. 2010 May;40(3):357-65. doi: 10.1007/s10519-009-9314-8. Epub 2009 Nov 26.

PMID:
19941049
5.

The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.

Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Tan EK, Drozdzik M.

Pharmacogenet Genomics. 2008 Sep;18(9):815-21. doi: 10.1097/FPC.0b013e328306c2f2.

PMID:
18698234
6.
7.

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
8.

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
9.

Epistasis effects of COMT and MTHFR on inter-individual differences in mental health: under the inverted U-shaped prefrontal dopamine model.

Htun NC, Miyaki K, Zhao C, Muramatsu M, Sato N.

Biochem Biophys Res Commun. 2014 Sep 5;451(4):574-9. doi: 10.1016/j.bbrc.2014.08.023. Epub 2014 Aug 12.

PMID:
25124664
10.

Association between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence.

Lohoff FW, Weller AE, Bloch PJ, Nall AH, Ferraro TN, Kampman KM, Pettinati HM, Oslin DW, Dackis CA, O'Brien CP, Berrettini WH.

Neuropsychopharmacology. 2008 Dec;33(13):3078-84. doi: 10.1038/npp.2008.126. Epub 2008 Aug 13.

11.

COMT Val158Met Genotype and Individual Differences in Executive Function in Healthy Adults.

Wishart HA, Roth RM, Saykin AJ, Rhodes CH, Tsongalis GJ, Pattin KA, Moore JH, McAllister TW.

J Int Neuropsychol Soc. 2011 Jan;17(1):174-80. doi: 10.1017/S1355617710001402. Epub 2010 Dec 10.

12.

Comprehensive assessment of genetic variation of catechol-O-methyltransferase and breast cancer risk.

Gaudet MM, Chanock S, Lissowska J, Berndt SI, Peplonska B, Brinton LA, Welch R, Yeager M, Bardin-Mikolajczak A, Garcia-Closas M.

Cancer Res. 2006 Oct 1;66(19):9781-5.

13.

COMT gene haplotypes are closely associated with postoperative fentanyl dose in patients.

Zhang F, Tong J, Hu J, Zhang H, Ouyang W, Huang D, Tang Q, Liao Q.

Anesth Analg. 2015 Apr;120(4):933-40. doi: 10.1213/ANE.0000000000000563.

PMID:
25532715
14.

Gender-specific effects of the catechol-O-methyltransferase Val108/158Met polymorphism on cognitive function in children.

Barnett JH, Heron J, Ring SM, Golding J, Goldman D, Xu K, Jones PB.

Am J Psychiatry. 2007 Jan;164(1):142-9.

PMID:
17202556
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.

Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision.

Bortsov AV, Diatchenko L, McLean SA.

Neuromolecular Med. 2014 Mar;16(1):83-93. doi: 10.1007/s12017-013-8255-9. Epub 2013 Aug 21.

17.

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.

Carmel M, Zarchi O, Michaelovsky E, Frisch A, Patya M, Green T, Gothelf D, Weizman A.

J Psychiatr Res. 2014 Sep;56:28-35. doi: 10.1016/j.jpsychires.2014.04.019. Epub 2014 May 9.

PMID:
24853458
18.

COMT haplotypes modulate associations of antenatal maternal anxiety and neonatal cortical morphology.

Qiu A, Tuan TA, Ong ML, Li Y, Chen H, Rifkin-Graboi A, Broekman BF, Kwek K, Saw SM, Chong YS, Gluckman PD, Fortier MV, Holbrook JD, Meaney MJ.

Am J Psychiatry. 2015 Feb 1;172(2):163-72. doi: 10.1176/appi.ajp.2014.14030313. Epub 2014 Oct 31.

PMID:
25320962
19.

Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.

Rakvåg TT, Ross JR, Sato H, Skorpen F, Kaasa S, Klepstad P.

Mol Pain. 2008 Dec 18;4:64. doi: 10.1186/1744-8069-4-64.

20.

Dopamine inactivation efficacy related to functional DAT1 and COMT variants influences motor response evaluation.

Bender S, Rellum T, Freitag C, Resch F, Rietschel M, Treutlein J, Jennen-Steinmetz C, Brandeis D, Banaschewski T, Laucht M.

PLoS One. 2012;7(5):e37814. doi: 10.1371/journal.pone.0037814. Epub 2012 May 23.

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