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Items: 17

1.

A Framework for Understanding the Emerging Role of Corticolimbic-Ventral Striatal Networks in OCD-Associated Repetitive Behaviors.

Wood J, Ahmari SE.

Front Syst Neurosci. 2015 Dec 17;9:171. doi: 10.3389/fnsys.2015.00171. eCollection 2015. Review.

2.

Genetic vulnerability in patients with psychiatric presentations: a neuroscience perspective.

Konopka LM.

Croat Med J. 2014 Oct;55(5):545-6. No abstract available.

3.

Association of the catechol-O-methyltransferase val158met polymorphism and anxiety-related traits: a meta-analysis.

Lee LO, Prescott CA.

Psychiatr Genet. 2014 Apr;24(2):52-69. doi: 10.1097/YPG.0000000000000018.

4.

Orofacial pain prospective evaluation and risk assessment study--the OPPERA study.

Maixner W, Diatchenko L, Dubner R, Fillingim RB, Greenspan JD, Knott C, Ohrbach R, Weir B, Slade GD.

J Pain. 2011 Nov;12(11 Suppl):T4-11.e1-2. doi: 10.1016/j.jpain.2011.08.002. No abstract available.

5.

The genetics of obsessive-compulsive disorder: a review.

Pauls DL.

Dialogues Clin Neurosci. 2010;12(2):149-63. Review.

6.

Anxiety disorders in children with williams syndrome, their mothers, and their siblings: implications for the etiology of anxiety disorders.

Leyfer O, Woodruff-Borden J, Mervis CB.

J Neurodev Disord. 2009 Mar;1(1):4-14. doi: 10.1007/s11689-009-9003-1.

7.

Genetics of obsessive-compulsive disorder.

Nestadt G, Grados M, Samuels JF.

Psychiatr Clin North Am. 2010 Mar;33(1):141-58. doi: 10.1016/j.psc.2009.11.001. Review.

8.

Modeling complex genetic and environmental influences on comorbid bipolar disorder with tobacco use disorder.

McEachin RC, Saccone NL, Saccone SF, Kleyman-Smith YD, Kar T, Kare RK, Ade AS, Sartor MA, Cavalcoli JD, McInnis MG.

BMC Med Genet. 2010 Jan 26;11:14. doi: 10.1186/1471-2350-11-14.

9.

Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.

Delorme R, Betancur C, Chaste P, Kernéis S, Stopin A, Mouren MC, Collet C, Bourgeron T, Leboyer M, Launay JM.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-548. doi: 10.1002/ajmg.b.31016.

10.

Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.

Nackley AG, Shabalina SA, Lambert JE, Conrad MS, Gibson DG, Spiridonov AN, Satterfield SK, Diatchenko L.

PLoS One. 2009;4(4):e5237. doi: 10.1371/journal.pone.0005237. Epub 2009 Apr 13.

11.

Assessing the validity of current mouse genetic models of obsessive-compulsive disorder.

Wang L, Simpson HB, Dulawa SC.

Behav Pharmacol. 2009 Mar;20(2):119-33. doi: 10.1097/FBP.0b013e32832a80ad. Review.

12.

Executive attention in schizophrenic males and the impact of COMT Val108/158Met genotype on performance on the attention network test.

Opgen-Rhein C, Neuhaus AH, Urbanek C, Hahn E, Sander T, Dettling M.

Schizophr Bull. 2008 Nov;34(6):1231-9. doi: 10.1093/schbul/sbm155. Epub 2008 Jan 16.

13.

The OCD collaborative genetics study: methods and sample description.

Samuels JF, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Pinto A, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Bienvenu OJ 3rd, Rasmussen SA, Pauls DL, Willour VL, Shugart YY, Liang KY, Hoehn-Saric R, Nestadt G.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):201-7.

14.

A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).

Kates WR, Antshel KM, Abdulsabur N, Colgan D, Funke B, Fremont W, Higgins AM, Kucherlapati R, Shprintzen RJ.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):274-80.

15.

COMT genetic variation confers risk for psychotic and affective disorders: a case control study.

Funke B, Malhotra AK, Finn CT, Plocik AM, Lake SL, Lencz T, DeRosse P, Kane JM, Kucherlapati R.

Behav Brain Funct. 2005 Oct 18;1:19.

16.

Linkage analysis of ordinal traits for pedigree data.

Feng R, Leckman JF, Zhang H.

Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16739-44. Epub 2004 Nov 17.

17.

Assessing the molecular genetics of attention networks.

Fossella J, Sommer T, Fan J, Wu Y, Swanson JM, Pfaff DW, Posner MI.

BMC Neurosci. 2002 Oct 4;3:14.

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