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Items: 1 to 20 of 367

1.

COMT Val158Met modulates the effect of childhood adverse experiences on the risk of alcohol dependence.

Schellekens AF, Franke B, Ellenbroek B, Cools A, de Jong CA, Buitelaar JK, Verkes RJ.

Addict Biol. 2013 Mar;18(2):344-56. doi: 10.1111/j.1369-1600.2012.00438.x. Epub 2012 Apr 17.

PMID:
22509987
2.

Reduced dopamine receptor sensitivity as an intermediate phenotype in alcohol dependence and the role of the COMT Val158Met and DRD2 Taq1A genotypes.

Schellekens AF, Franke B, Ellenbroek B, Cools A, de Jong CA, Buitelaar JK, Verkes RJ.

Arch Gen Psychiatry. 2012 Apr;69(4):339-48. doi: 10.1001/archgenpsychiatry.2011.1335.

PMID:
22474103
3.

Double dissociation of dopamine genes and timing in humans.

Wiener M, Lohoff FW, Coslett HB.

J Cogn Neurosci. 2011 Oct;23(10):2811-21. doi: 10.1162/jocn.2011.21626. Epub 2011 Jan 24.

PMID:
21261454
4.

Family-based and case-control study of DRD2, DAT, 5HTT, COMT genes polymorphisms in alcohol dependence.

Samochowiec J, Kucharska-Mazur J, Grzywacz A, Jabłoński M, Rommelspacher H, Samochowiec A, Sznabowicz M, Horodnicki J, Sagan L, Pełka-Wysiecka J.

Neurosci Lett. 2006 Dec 13;410(1):1-5. Epub 2006 Oct 31.

PMID:
17079080
5.

Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1.

Dick DM, Wang JC, Plunkett J, Aliev F, Hinrichs A, Bertelsen S, Budde JP, Goldstein EL, Kaplan D, Edenberg HJ, Nurnberger J Jr, Hesselbrock V, Schuckit M, Kuperman S, Tischfield J, Porjesz B, Begleiter H, Bierut LJ, Goate A.

Alcohol Clin Exp Res. 2007 Oct;31(10):1645-53.

PMID:
17850642
6.

Impact of COMT Val 108/158 Met and DRD2 Taq1B gene polymorphisms on vulnerability to cigarette smoking of Thai males.

Suriyaprom K, Tungtrongchitr R, Harnroongroj T.

J Mol Neurosci. 2013 Mar;49(3):544-9. doi: 10.1007/s12031-012-9844-z. Epub 2012 Jun 28.

PMID:
22740151
7.

Putative role of the COMT gene polymorphism (Val158Met) on verbal working memory functioning in a healthy population.

Aguilera M, Barrantes-Vidal N, Arias B, Moya J, Villa H, Ibáñez MI, Ruipérez MA, Ortet G, Fañanás L.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):898-902. doi: 10.1002/ajmg.b.30705.

PMID:
18213617
8.

The association study of polymorphisms in DAT, DRD2, and COMT genes and acute extrapyramidal adverse effects in male schizophrenic patients treated with haloperidol.

Zivković M, Mihaljević-Peles A, Bozina N, Sagud M, Nikolac-Perkovic M, Vuksan-Cusa B, Muck-Seler D.

J Clin Psychopharmacol. 2013 Oct;33(5):593-9. doi: 10.1097/JCP.0b013e31829abec9.

PMID:
23963056
9.

DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability.

Xu H, Kellendonk CB, Simpson EH, Keilp JG, Bruder GE, Polan HJ, Kandel ER, Gilliam TC.

Schizophr Res. 2007 Feb;90(1-3):104-7. Epub 2006 Nov 17.

PMID:
17113268
10.

Interaction between catechol-O-methyltransferase (COMT) Val158Met genotype and genetic vulnerability to schizophrenia during explicit processing of aversive facial stimuli.

Lo Bianco L, Blasi G, Taurisano P, Di Giorgio A, Ferrante F, Ursini G, Fazio L, Gelao B, Romano R, Papazacharias A, Caforio G, Sinibaldi L, Popolizio T, Bellantuono C, Bertolino A.

Psychol Med. 2013 Feb;43(2):279-92. doi: 10.1017/S0033291712001134. Epub 2012 May 23.

PMID:
22617427
11.

Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy.

Huuhka K, Anttila S, Huuhka M, Hietala J, Huhtala H, Mononen N, Lehtimäki T, Leinonen E.

Neurosci Lett. 2008 Dec 19;448(1):79-83. doi: 10.1016/j.neulet.2008.10.015. Epub 2008 Oct 9.

PMID:
18929622
12.

COMT gene val158met polymorphism in patients with dyspeptic symptoms.

Tahara T, Arisawa T, Shibata T, Nakamura M, Wang F, Hirata I.

Hepatogastroenterology. 2008 May-Jun;55(84):979-82.

PMID:
18705311
13.

The flexible mind is associated with the catechol-O-methyltransferase (COMT) Val158Met polymorphism: evidence for a role of dopamine in the control of task-switching.

Colzato LS, Waszak F, Nieuwenhuis S, Posthuma D, Hommel B.

Neuropsychologia. 2010 Jul;48(9):2764-8. doi: 10.1016/j.neuropsychologia.2010.04.023. Epub 2010 Apr 29.

PMID:
20434465
14.

COMT Val158Met-stress interaction in psychosis: role of background psychosis risk.

Collip D, van Winkel R, Peerbooms O, Lataster T, Thewissen V, Lardinois M, Drukker M, Rutten BP, Van Os J, Myin-Germeys I.

CNS Neurosci Ther. 2011 Dec;17(6):612-9. doi: 10.1111/j.1755-5949.2010.00213.x. Epub 2010 Nov 14.

PMID:
21073668
15.

The association of DRD2 -141C and ANKK1 TaqIA polymorphisms with alcohol dependence in Korean population classified by the Lesch typology.

Lee SH, Lee BH, Lee JS, Chai YG, Choi MR, Han DM, Ji H, Jang GH, Shin HE, Choi IG.

Alcohol Alcohol. 2013 Jul-Aug;48(4):426-32. doi: 10.1093/alcalc/agt029. Epub 2013 Apr 4.

PMID:
23558112
16.

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.

Bellgrove MA, Domschke K, Hawi Z, Kirley A, Mullins C, Robertson IH, Gill M.

Exp Brain Res. 2005 Jun;163(3):352-60. Epub 2005 Jan 15.

PMID:
15654584
17.

[No association between catechol-O-methyltransferase val158met polymorphism and alexithymia].

Hermes S, Hennig J, Stingl M, Leichsenring F, Leweke F.

Z Psychosom Med Psychother. 2011;57(1):51-61. German.

PMID:
21432838
18.

Association study of the SLC6A3 VNTR (DAT) and DRD2/ANKK1 Taq1A polymorphisms with alcohol dependence in a population from northeastern Brazil.

Vasconcelos AC, Neto Ede S, Pinto GR, Yoshioka FK, Motta FJ, Vasconcelos DF, Canalle R.

Alcohol Clin Exp Res. 2015 Feb;39(2):205-11. doi: 10.1111/acer.12625.

PMID:
25684044
19.

Association of COMT val158met and DRD2 G>T genetic polymorphisms with individual differences in motor learning and performance in female young adults.

Noohi F, Boyden NB, Kwak Y, Humfleet J, Burke DT, Müller ML, Bohnen NI, Seidler RD.

J Neurophysiol. 2014 Feb;111(3):628-40. doi: 10.1152/jn.00457.2013. Epub 2013 Nov 13.

20.

Effects of dopamine-related gene-gene interactions on working memory component processes.

Stelzel C, Basten U, Montag C, Reuter M, Fiebach CJ.

Eur J Neurosci. 2009 Mar;29(5):1056-63. doi: 10.1111/j.1460-9568.2009.06647.x.

PMID:
19291230

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