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Items: 1 to 20 of 176

1.

Association between 7q31 markers and Tourette syndrome.

Díaz-Anzaldúa A, Joober R, Rivière JB, Dion Y, Lespérance P, Chouinard S, Richer F, Rouleau GA.

Am J Med Genet A. 2004 May 15;127A(1):17-20.

PMID:
15103711
2.

[Transmission disequilibrium test of DRD4 exon III 48bp variant number tandem repeat polymorphism and tic disorder].

Huang Y, Liu X, Li T, Guo L, Ma X, Yuan G, Peng R.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Apr;19(2):100-3. Chinese.

PMID:
11941581
3.

Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism.

Qian Q, Wang Y, Zhou R, Li J, Wang B, Glatt S, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):103-9.

PMID:
12627475
4.

Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population.

Díaz-Anzaldúa A, Joober R, Rivière JB, Dion Y, Lespérance P, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Syndrome Study Group.

Mol Psychiatry. 2004 Mar;9(3):272-7.

PMID:
15094788
5.

[Cases-Control association study and transmission disequilibrium test of T102C polymorphism in 5HT2A and Tourette syndrome].

Huang Y, Liu X, Li T, Guo L, Sun X, Xiao X, Ma X, Wang Y, Collier DA.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Feb;18(1):11-3. Chinese.

PMID:
11172633
6.

A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD).

Banerjee E, Sinha S, Chatterjee A, Gangopadhyay PK, Singh M, Nandagopal K.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):361-6.

PMID:
16583436
7.

Association of intronic variants of the BTBD9 gene with Tourette syndrome.

Rivière JB, Xiong L, Levchenko A, St-Onge J, Gaspar C, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Study Group.

Arch Neurol. 2009 Oct;66(10):1267-72. doi: 10.1001/archneurol.2009.213.

PMID:
19822783
8.

Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population.

Díaz-Anzaldúa A, Rivière JB, Dubé MP, Joober R, Saint-Onge J, Dion Y, Lespérance P, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Syndrome Study Group.

Am J Med Genet A. 2005 Oct 15;138A(3):225-8.

PMID:
16158425
10.

Dopaminergic polymorphisms in Tourette syndrome: association with the DAT gene (SLC6A3).

Yoon DY, Rippel CA, Kobets AJ, Morris CM, Lee JE, Williams PN, Bridges DD, Vandenbergh DJ, Shugart YY, Singer HS.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jul 5;144B(5):605-10.

PMID:
17171650
11.

Evidence for the gamma-amino-butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive-compulsive disorder.

Zai G, Arnold P, Burroughs E, Barr CL, Richter MA, Kennedy JL.

Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):25-9.

PMID:
15685626
12.

Do obsessive-compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population.

Liu S, Cui J, Niu Z, Yi M, Zhang X, Che F, Ma X.

World J Biol Psychiatry. 2015;16(8):602-9. doi: 10.3109/15622975.2015.1012226. Epub 2015 Mar 14.

PMID:
25771937
13.

Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder.

McDougle CJ, Epperson CN, Price LH, Gelernter J.

Mol Psychiatry. 1998 May;3(3):270-3.

PMID:
9672904
14.

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.

Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K.

Am J Hum Genet. 2001 Apr;68(4):848-58. Epub 2001 Mar 9.

15.

Association of IL8 -251A/T, IL12B -1188A/C and TNF-α -238A/G polymorphisms with Tourette syndrome in a family-based association study in a Chinese Han population.

Liu S, Yi M, Wang M, Sun Y, Che F, Ma X.

Neurosci Lett. 2011 May 16;495(2):155-8. doi: 10.1016/j.neulet.2011.03.060. Epub 2011 Apr 2.

PMID:
21443923
16.

No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.

Jiang SD, Wu XD, Zhang Y, Tang GM, Qian YP, Wang DX.

Yi Chuan Xue Bao. 2005 Aug;32(8):784-8.

PMID:
16231731
17.

Serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder in Chinese Han subjects.

Li J, Wang Y, Zhou R, Zhang H, Yang L, Wang B, Khan S, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):59-63.

PMID:
15578608
18.

A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.

Stewart SE, Platko J, Fagerness J, Birns J, Jenike E, Smoller JW, Perlis R, Leboyer M, Delorme R, Chabane N, Rauch SL, Jenike MA, Pauls DL.

Arch Gen Psychiatry. 2007 Feb;64(2):209-14.

PMID:
17283288
19.
20.

Association of the dopamine D5 receptor with attention deficit hyperactivity disorder (ADHD) and scores on a continuous performance test (TOVA).

Manor I, Corbex M, Eisenberg J, Gritsenkso I, Bachner-Melman R, Tyano S, Ebstein RP.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):73-7.

PMID:
15108184

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