Yang Y - Search Results

1

Novel THAP1 gene mutations in patients with primary dystonia from southwest China.

Song W, Chen Y, Huang R, Chen K, Pan P, Yang Y, Shang HF. Song W, et al. Among authors: yang y. J Neurol Sci. 2011 Oct 15;309(1-2):63-7. doi: 10.1016/j.jns.2011.07.023. Epub 2011 Aug 11. J Neurol Sci. 2011. PMID: 21839475

2

GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.

Liu X, Zhang SS, Fang DF, Ma MY, Guo XY, Yang Y, Shang HF. Liu X, et al. Among authors: yang y. Mov Disord. 2010 Mar 15;25(4):447-51. doi: 10.1002/mds.22976. Mov Disord. 2010. PMID: 20108370 Clinical Trial.

3

TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis.

Huang R, Fang DF, Ma MY, Guo XY, Zhao B, Zeng Y, Zhou D, Yang Y, Shang HF. Huang R, et al. Among authors: yang y. Neurobiol Aging. 2012 May;33(5):1015.e1-6. doi: 10.1016/j.neurobiolaging.2010.07.007. Epub 2010 Aug 13. Neurobiol Aging. 2012. PMID: 20708823

4

Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.

Ma M, Yang Y, Shang H, Su D, Zhang H, Ma Y, Liu Y, Tao D, Zhang S. Ma M, et al. Among authors: yang y. J Neurol Sci. 2010 Nov 15;298(1-2):57-60. doi: 10.1016/j.jns.2010.08.024. J Neurol Sci. 2010. PMID: 20864123

5

GLIS1 rs797906: an increased risk factor for late-onset Parkinson's disease in the Han Chinese population.

Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF. Song W, et al. Among authors: yang y. Eur Neurol. 2012;68(2):89-92. doi: 10.1159/000337955. Epub 2012 Jul 3. Eur Neurol. 2012. PMID: 22759478

6

Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.

Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake W, Toda T, Shang HF. Chen K, et al. Among authors: yang y. Neurol Res. 2012 Sep;34(7):725-9. doi: 10.1179/1743132812Y.0000000075. Neurol Res. 2012. PMID: 22889673

7

PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.

Chen Y, Zheng ZZ, Huang R, Chen K, Song W, Zhao B, Chen X, Yang Y, Yuan L, Shang HF. Chen Y, et al. Among authors: yang y. Neurobiol Aging. 2013 Jul;34(7):1922.e1-5. doi: 10.1016/j.neurobiolaging.2013.01.013. Epub 2013 Feb 19. Neurobiol Aging. 2013. PMID: 23428184

8

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.

Chen YP, Song W, Huang R, Chen K, Zhao B, Li J, Yang Y, Shang HF. Chen YP, et al. Among authors: yang y. J Clin Neurosci. 2013 Jun;20(6):880-3. doi: 10.1016/j.jocn.2012.07.011. Epub 2013 Apr 23. J Clin Neurosci. 2013. PMID: 23618683

9

SQSTM1 mutations in Han Chinese populations with sporadic amyotrophic lateral sclerosis.

Chen Y, Zheng ZZ, Chen X, Huang R, Yang Y, Yuan L, Pan L, Hadano S, Shang HF. Chen Y, et al. Among authors: yang y. Neurobiol Aging. 2014 Mar;35(3):726.e7-9. doi: 10.1016/j.neurobiolaging.2013.09.008. Epub 2013 Oct 15. Neurobiol Aging. 2014. PMID: 24138988

10

Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.

Chen X, Huang R, Chen Y, Zheng Z, Chen K, Song W, Zhao B, Yang Y, Yuan L, Shang H. Chen X, et al. Among authors: yang y. Neurol Sci. 2014 Jul;35(7):1089-95. doi: 10.1007/s10072-014-1656-1. Epub 2014 Feb 4. Neurol Sci. 2014. PMID: 24493373

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