Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 117

Similar articles for PubMed (Select 23728717)

1.

Common functional polymorphisms in SLC6A4 and COMT genes are associated with circadian phenotypes in a South American sample.

Ojeda DA, Perea CS, Suárez A, Niño CL, Gutiérrez RM, López-León S, Adan A, Arboleda H, Camargo A, Forero DA.

Neurol Sci. 2014 Jan;35(1):41-7. doi: 10.1007/s10072-013-1466-x. Epub 2013 Jun 1.

PMID:
23728717
2.

A novel association of two non-synonymous polymorphisms in PER2 and PER3 genes with specific diurnal preference subscales.

Ojeda DA, Perea CS, Niño CL, Gutiérrez RM, López-León S, Arboleda H, Camargo A, Adan A, Forero DA.

Neurosci Lett. 2013 Oct 11;553:52-6. doi: 10.1016/j.neulet.2013.08.016. Epub 2013 Aug 19.

PMID:
23969301
3.

COMT Val158Met × SLC6A4 5-HTTLPR interaction impacts on gray matter volume of regions supporting emotion processing.

Radua J, El-Hage W, Monté GC, Gohier B, Tropeano M, Phillips ML, Surguladze SA.

Soc Cogn Affect Neurosci. 2014 Aug;9(8):1232-8. doi: 10.1093/scan/nst089. Epub 2013 Jun 6.

PMID:
23748501
4.

Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD.

Nijmeijer JS, Hartman CA, Rommelse NN, Altink ME, Buschgens CJ, Fliers EA, Franke B, Minderaa RB, Ormel J, Sergeant JA, Verhulst FC, Buitelaar JK, Hoekstra PJ.

J Child Psychol Psychiatry. 2010 Nov;51(11):1242-50. doi: 10.1111/j.1469-7610.2010.02277.x. Epub 2010 Sep 24.

5.

Serotonin transporter and BDNF polymorphisms interact to predict trait worry.

Bredemeier K, Beevers CG, McGeary JE.

Anxiety Stress Coping. 2014;27(6):712-21. doi: 10.1080/10615806.2014.909928. Epub 2014 Apr 25.

PMID:
24679122
6.

Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample.

Perea CS, Niño CL, López-León S, Gutiérrez R, Ojeda D, Arboleda H, Camargo A, Adan A, Forero DA.

Open Neurol J. 2014 Apr 18;8:7-10. doi: 10.2174/1874205X01408010007. eCollection 2014.

7.

COMT val158met and 5-HTTLPR genetic polymorphisms moderate executive control in cannabis users.

Verdejo-García A, Fagundo AB, Cuenca A, Rodriguez J, Cuyás E, Langohr K, de Sola Llopis S, Civit E, Farré M, Peña-Casanova J, de la Torre R.

Neuropsychopharmacology. 2013 Jul;38(8):1598-606. doi: 10.1038/npp.2013.59. Epub 2013 Feb 28.

8.

Genetic polymorphisms of DAT1 and COMT differentially associate with actigraphy-derived sleep-wake cycles in young adults.

Valomon A, Holst SC, Bachmann V, Viola AU, Schmidt C, Zürcher J, Berger W, Cajochen C, Landolt HP.

Chronobiol Int. 2014 Jun;31(5):705-14. doi: 10.3109/07420528.2014.896376. Epub 2014 Mar 13.

PMID:
24625311
10.

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
11.

Functional polymorphisms in COMT and SLC6A4 genes influence the prognosis of patients with medication overuse headache after withdrawal therapy.

Cargnin S, Viana M, Ghiotto N, Bianchi M, Sances G, Tassorelli C, Nappi G, Canonico PL, Genazzani AA, Terrazzino S.

Eur J Neurol. 2014 Jul;21(7):989-95. doi: 10.1111/ene.12424. Epub 2014 Mar 29.

PMID:
24684248
12.

[Association between aggressive behaviors and COMT Val158Met and 5-HTTLPR polymorphisms in children].

Cao YP, Li LF, Zhao XF, Zhang YL.

Zhongguo Dang Dai Er Ke Za Zhi. 2011 May;13(5):361-4. Chinese.

13.

Association between the catechol O-methyltransferase Val108/158Met polymorphism and alexithymia.

Ham BJ, Lee MS, Lee YM, Kim MK, Choi MJ, Oh KS, Jung HY, Lyoo IK, Choi IG.

Neuropsychobiology. 2005;52(3):151-4.

PMID:
16127282
14.

Interaction of chronic stress with serotonin transporter and catechol-O-methyltransferase polymorphisms in predicting youth depression.

Conway CC, Hammen C, Brennan PA, Lind PA, Najman JM.

Depress Anxiety. 2010 Aug;27(8):737-45. doi: 10.1002/da.20715.

15.

Interaction between gene variants of the serotonin transporter promoter region (5-HTTLPR) and catechol O-methyltransferase (COMT) in borderline personality disorder.

Tadić A, Victor A, Başkaya O, von Cube R, Hoch J, Kouti I, Anicker NJ, Höppner W, Lieb K, Dahmen N.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):487-95. doi: 10.1002/ajmg.b.30843.

PMID:
18756498
16.

Genetic risk for conduct disorder symptom subtypes in an ADHD sample: specificity to aggressive symptoms.

Monuteaux MC, Biederman J, Doyle AE, Mick E, Faraone SV.

J Am Acad Child Adolesc Psychiatry. 2009 Jul;48(7):757-64. doi: 10.1097/CHI.0b013e3181a5661b.

PMID:
19465875
17.

Catechol-O-methyltransferase gene variation: impact on amygdala response to aversive stimuli.

Domschke K, Baune BT, Havlik L, Stuhrmann A, Suslow T, Kugel H, Zwanzger P, Grotegerd D, Sehlmeyer C, Arolt V, Dannlowski U.

Neuroimage. 2012 May 1;60(4):2222-9. doi: 10.1016/j.neuroimage.2012.02.039. Epub 2012 Feb 23.

PMID:
22387174
18.

Relation of shyness in grade school children to the genotype for the long form of the serotonin transporter promoter region polymorphism.

Arbelle S, Benjamin J, Golin M, Kremer I, Belmaker RH, Ebstein RP.

Am J Psychiatry. 2003 Apr;160(4):671-6.

PMID:
12668354
19.

Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.

Biederman J, Kim JW, Doyle AE, Mick E, Fagerness J, Smoller JW, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1511-8. doi: 10.1002/ajmg.b.30874.

20.

Daytime sleepiness and the COMT val158met polymorphism in patients with Parkinson disease.

Rissling I, Frauscher B, Kronenberg F, Tafti M, Stiasny-Kolster K, Robyr AC, Körner Y, Oertel WH, Poewe W, Högl B, Möller JC.

Sleep. 2006 Jan;29(1):108-11.

PMID:
16453988
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk