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Items: 1 to 20 of 80

1.

[Genetic aspects of the Stroop test].

Nánási T, Katonai ER, Sasvári-Székely M, Székely A.

Neuropsychopharmacol Hung. 2012 Dec;14(4):252-8. Review. Hungarian.

2.

The Met66 allele of the functional Val66Met polymorphism in the brain-derived neurotrophic factor gene confers protection against neurocognitive dysfunction in systemic lupus erythematosus.

Oroszi G, Lapteva L, Davis E, Yarboro CH, Weickert T, Roebuck-Spencer T, Bleiberg J, Rosenstein D, Pao M, Lipsky PE, Goldman D, Lipsky RH, Illei GG.

Ann Rheum Dis. 2006 Oct;65(10):1330-5. Epub 2006 Apr 10.

3.

The genetics of cognitive ability and cognitive ageing in healthy older people.

Harris SE, Deary IJ.

Trends Cogn Sci. 2011 Sep;15(9):388-94. doi: 10.1016/j.tics.2011.07.004. Epub 2011 Aug 15.

PMID:
21840749
4.

The genetic background to PTSD.

Broekman BF, Olff M, Boer F.

Neurosci Biobehav Rev. 2007;31(3):348-62. Epub 2006 Nov 28. Review.

PMID:
17126903
5.

Effects of COMT, DRD2, BDNF, and APOE Genotypic Variation on Treatment Efficacy and Cognitive Side Effects of Electroconvulsive Therapy.

Bousman CA, Katalinic N, Martin DM, Smith DJ, Ingram A, Dowling N, Ng C, Loo CK.

J ECT. 2015 Jun;31(2):129-35. doi: 10.1097/YCT.0000000000000170.

PMID:
25148110
6.

Synergistic effects of the apolipoprotein E epsilon3/epsilon2/epsilon4, the cholesteryl ester transfer protein TaqIB, and the apolipoprotein C3 -482 C>T polymorphisms on their association with coronary artery disease.

Muendlein A, Saely CH, Marte T, Schmid F, Koch L, Rein P, Langer P, Aczel S, Drexel H.

Atherosclerosis. 2008 Jul;199(1):179-86. doi: 10.1016/j.atherosclerosis.2007.10.030. Epub 2008 Mar 4.

PMID:
18289550
7.

Stroop performance in major depression: selective attention impairment or psychomotor slowness?

Kertzman S, Reznik I, Hornik-Lurie T, Weizman A, Kotler M, Amital D.

J Affect Disord. 2010 Apr;122(1-2):167-73. doi: 10.1016/j.jad.2009.08.009. Epub 2009 Sep 4.

PMID:
19732958
8.

Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.

Liu L, Guan LL, Chen Y, Ji N, Li HM, Li ZH, Qian QJ, Yang L, Glatt SJ, Faraone SV, Wang YF.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):737-48. doi: 10.1002/ajmg.b.31217. Epub 2011 Jul 14.

PMID:
21761555
9.

Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease.

Nacmias B, Piccini C, Bagnoli S, Tedde A, Cellini E, Bracco L, Sorbi S.

Neurosci Lett. 2004 Sep 9;367(3):379-83.

PMID:
15337270
10.

The effect of the APOE-epsilon4 allele and ACE-I/D polymorphism on cognition during a two-year follow-up in first-ever stroke patients.

Bour AM, Rasquin SM, Baars L, van Boxtel MP, Visser PJ, Limburg M, Verhey FR.

Dement Geriatr Cogn Disord. 2010;29(6):534-42. doi: 10.1159/000314678. Epub 2010 Jul 1.

PMID:
20606435
11.

The molecular genetics of cognition: dopamine, COMT and BDNF.

Savitz J, Solms M, Ramesar R.

Genes Brain Behav. 2006 Jun;5(4):311-28. Review.

12.

Enduring cognitive dysfunction in unipolar major depression: a test-retest study using the Stroop paradigm.

Hammar A, Sørensen L, Ardal G, Oedegaard KJ, Kroken R, Roness A, Lund A.

Scand J Psychol. 2010 Aug;51(4):304-8. doi: 10.1111/j.1467-9450.2009.00765.x. Epub 2009 Dec 23.

PMID:
20042028
13.

A polymorphism of the brain-derived neurotrophic factor (BDNF) is associated with Alzheimer's disease in patients lacking the Apolipoprotein E epsilon4 allele.

Riemenschneider M, Schwarz S, Wagenpfeil S, Diehl J, Müller U, Förstl H, Kurz A.

Mol Psychiatry. 2002;7(7):782-5.

14.

An APOA1 promoter polymorphism is associated with cognitive performance in patients with multiple sclerosis.

Koutsis G, Panas M, Giogkaraki E, Karadima G, Sfagos C, Vassilopoulos D.

Mult Scler. 2009 Feb;15(2):174-9. doi: 10.1177/1352458508097217. Epub 2008 Sep 19.

PMID:
18805838
15.

Dopamine β-hydroxylase gene associates with stroop color-word task performance in Han Chinese children with attention deficit/hyperactivity disorder.

Ji N, Shuai L, Chen Y, Liu L, Li HM, Li ZH, Yang L, Qian QJ, Tang YL, Cubells JF, Wang YF.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):730-6. doi: 10.1002/ajmg.b.31215. Epub 2011 Jul 14.

PMID:
21761554
16.

Do apolipoprotein E genotype and educational attainment predict the rate of cognitive decline in normal aging? A 12-year follow-up of the Maastricht Aging Study.

Van Gerven PW, Van Boxtel MP, Ausems EE, Bekers O, Jolles J.

Neuropsychology. 2012 Jul;26(4):459-72. doi: 10.1037/a0028685. Epub 2012 May 28.

PMID:
22642392
17.

Genotype and childhood sexual trauma moderate neurocognitive performance: a possible role for brain-derived neurotrophic factor and apolipoprotein E variants.

Savitz J, van der Merwe L, Stein DJ, Solms M, Ramesar R.

Biol Psychiatry. 2007 Sep 1;62(5):391-9. Epub 2007 Jan 8.

PMID:
17210134
18.

Alzheimer's disease genes and cognition in the nondemented general population.

Verhaaren BF, Vernooij MW, Koudstaal PJ, Uitterlinden AG, van Duijn CM, Hofman A, Breteler MM, Ikram MA.

Biol Psychiatry. 2013 Mar 1;73(5):429-34. doi: 10.1016/j.biopsych.2012.04.009. Epub 2012 May 15.

PMID:
22592056
19.

APOE polymorphism affects episodic memory among non demented elderly subjects.

De Blasi S, Montesanto A, Martino C, Dato S, De Rango F, Bruni AC, Mari V, Feraco E, Passarino G.

Exp Gerontol. 2009 Mar;44(3):224-7. doi: 10.1016/j.exger.2008.11.005. Epub 2008 Nov 24.

PMID:
19059330
20.

Functional genetic polymorphisms in serotonin and dopamine gene systems and their significance in behavioural disorders.

D'Souza UM, Craig IW.

Prog Brain Res. 2008;172:73-98. doi: 10.1016/S0079-6123(08)00904-7. Review.

PMID:
18772028

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