156 related articles for article (PubMed ID: 25297601)
1. [Association of serotonin transporter linked polymorphic region 44 bp variable number of tandem repeat polymorphism with Tourette syndrome].
Zhang Y; Su N; Wang G; Cui J; Yi M; Liu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):646-9. PubMed ID: 25297601
[TBL] [Abstract][Full Text] [Related]
2. [Family-based association study of a variable number of tandem repeat polymorphism of DAT1 gene with Tourette syndrome in a Chinese Han population].
Zheng L; Han ZL; Zhang XH; Wang XQ; Jiang WH; Yi MJ; Liu SG
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):594-7. PubMed ID: 24078578
[TBL] [Abstract][Full Text] [Related]
3. Association between the polymorphism of C861G (rs6296) in the serotonin 1B receptor gene and Tourette syndrome in Han Chinese people.
Yi M; Zhang Y; Wang Y; Su N; Liu S
Asia Pac Psychiatry; 2017 Jun; 9(2):. PubMed ID: 26123080
[TBL] [Abstract][Full Text] [Related]
4. 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; 495(2):155-8. PubMed ID: 21443923
[TBL] [Abstract][Full Text] [Related]
5. The role of GRIN2B in Tourette syndrome: Results from a transmission disequilibrium study.
Che F; Zhang Y; Wang G; Heng X; Liu S; Du Y
J Affect Disord; 2015 Nov; 187():62-5. PubMed ID: 26321256
[TBL] [Abstract][Full Text] [Related]
6. Association of IL-1α rs17561 and IL-1 RN rs315952 polymorphisms with Tourette syndrome: a family-based study.
He F; Shao X; Yi M; Wang Y; Wang CY; Liu S
Int J Clin Exp Pathol; 2015; 8(4):4182-5. PubMed ID: 26097611
[TBL] [Abstract][Full Text] [Related]
7. Choline acetyltransferase may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.
Yang X; Liu W; Yi M; Zhang R; Xu Y; Huang Z; Liu S; Li T
World J Biol Psychiatry; 2018 Oct; 19(7):521-526. PubMed ID: 28090804
[TBL] [Abstract][Full Text] [Related]
8. Lack of genetic association of 5-HTR2A 102 T/C and -1438A/G polymorphisms with Tourette syndrome in a family-based association study in a Chinese Han population.
Xu L; Zheng L; Ma J; Su N; Liu Y; Ma X; Zhang X; Liu S
Asia Pac Psychiatry; 2016 Mar; 8(1):87-91. PubMed ID: 25858583
[TBL] [Abstract][Full Text] [Related]
9. [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. PubMed ID: 11941581
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 25771937
[TBL] [Abstract][Full Text] [Related]
11. The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population.
Liu W; Zhang X; Deng Z; Li G; Zhang R; Yang Z; Che F; Liu S; Li H
J Gene Med; 2020 Jun; 22(6):e3173. PubMed ID: 32037697
[TBL] [Abstract][Full Text] [Related]
12. Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population.
Liu W; Qiu S; Gao C; Wang G; Liu S; Guan H
Neurosci Lett; 2017 Sep; 658():161-164. PubMed ID: 28830823
[TBL] [Abstract][Full Text] [Related]
13. Family-based association study between monoamine oxidase A (MAOA) gene promoter VNTR polymorphism and Tourette's syndrome in Chinese Han population.
Liu S; Wang X; Xu L; Zheng L; Ge Y; Ma X
Neurocase; 2015 Feb; 21(1):106-8. PubMed ID: 24422758
[TBL] [Abstract][Full Text] [Related]
14. Variable number tandem repeats in dopamine receptor D4 in Tourette's syndrome.
Liu S; Cui J; Zhang X; Wu W; Niu H; Ma X; Xu H; Yi M
Mov Disord; 2014 Nov; 29(13):1687-91. PubMed ID: 25258183
[TBL] [Abstract][Full Text] [Related]
15. [Transmission disequilibrium test of polymorphisms of serotonin transporter gene and schizophrenia based on family trios].
Sun WW; Fan JB; Qian XQ; Tang JX; Xing YL; Shi JG; Zhu SM; Liu HJ; Gu NF; Feng GY; He L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):342-4. PubMed ID: 12903048
[TBL] [Abstract][Full Text] [Related]
16. Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndrome.
Liu S; Yu X; Xu Q; Cui J; Yi M; Zhang X; Ge Y; Ma X
Sci Rep; 2015 Aug; 5():12687. PubMed ID: 26235311
[TBL] [Abstract][Full Text] [Related]
17. Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects.
Li J; Wang Y; Zhou R; Zhang H; Yang L; Wang B; Faraone SV
Am J Med Genet B Neuropsychiatr Genet; 2007 Jan; 144B(1):14-9. PubMed ID: 16941663
[TBL] [Abstract][Full Text] [Related]
18. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.
Cho IH; Yoo HJ; Park M; Lee YS; Kim SA
Brain Res; 2007 Mar; 1139():34-41. PubMed ID: 17280648
[TBL] [Abstract][Full Text] [Related]
19. Family-based association study of the serotonin transporter gene polymorphisms in Korean ADHD trios.
Kim SJ; Badner J; Cheon KA; Kim BN; Yoo HJ; Kim SJ; Cook E; Leventhal BL; Kim YS
Am J Med Genet B Neuropsychiatr Genet; 2005 Nov; 139B(1):14-8. PubMed ID: 16082698
[TBL] [Abstract][Full Text] [Related]
20. A meta-analysis of association studies between the 10-repeat allele of a VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention deficit hyperactivity disorder.
Yang B; Chan RC; Jing J; Li T; Sham P; Chen RY
Am J Med Genet B Neuropsychiatr Genet; 2007 Jun; 144B(4):541-50. PubMed ID: 17440978
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]