Sun QY - Search Results

1

Assessment of the association between NUS1 variants and essential tremor.

Yang HL, Jiang L, Pan HX, Xu K, Zhao YW, Liu ZH, Xu Q, Sun QY, Tan JQ, Li JC, Tang BS, Guo JF. Yang HL, et al. Among authors: sun qy. Neurosci Lett. 2021 Jan 1;740:135441. doi: 10.1016/j.neulet.2020.135441. Epub 2020 Oct 24. Neurosci Lett. 2021. PMID: 33184037

2

A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.

Wang L, Guo JF, Nie LL, Xu Q, Zuo X, Sun QY, Yan XX, Tang BS. Wang L, et al. Among authors: sun qy. Neurosci Lett. 2010 Jan 14;468(3):198-201. doi: 10.1016/j.neulet.2009.10.080. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879329

3

Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population.

Sun QY, Guo JF, Wang L, Yu RH, Zuo X, Yao LY, Pan Q, Xia K, Tang BS. Sun QY, et al. Mov Disord. 2010 Jun 15;25(8):1005-11. doi: 10.1002/mds.23009. Mov Disord. 2010. PMID: 20131388

4

Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population.

Zuo X, Jiang H, Guo JF, Yu RH, Sun QY, Hu L, Wang L, Yao LY, Shen L, Pan Q, Yan XX, Xia K, Tang BS. Zuo X, et al. Among authors: sun qy. Neurosci Lett. 2010 Sep 6;481(2):69-72. doi: 10.1016/j.neulet.2010.06.041. Epub 2010 Jun 19. Neurosci Lett. 2010. PMID: 20600614

5

LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's disease.

Yao LY, Guo JF, Wang L, Yu RH, Sun QY, Pan Q, Xia K, Tang BS, Shen L. Yao LY, et al. Among authors: sun qy. Neurosci Lett. 2011 May 9;495(1):35-8. doi: 10.1016/j.neulet.2011.03.030. Epub 2011 Mar 22. Neurosci Lett. 2011. PMID: 21406209

6

PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population.

Liu J, Sun QY, Tang BS, Hu L, Yu RH, Wang L, Shi CH, Yan XX, Pan Q, Xia K, Guo JF. Liu J, et al. Among authors: sun qy. Brain Res. 2011 May 25;1392:116-20. doi: 10.1016/j.brainres.2011.03.064. Epub 2011 Apr 6. Brain Res. 2011. PMID: 21524731

7

Variant in the 3' region of SNCA associated with Parkinson's disease and serum α-synuclein levels.

Hu Y, Tang B, Guo J, Wu X, Sun Q, Shi C, Hu L, Wang C, Wang L, Tan L, Shen L, Yan X, Zhang H. Hu Y, et al. J Neurol. 2012 Mar;259(3):497-504. doi: 10.1007/s00415-011-6209-4. Epub 2011 Aug 19. J Neurol. 2012. PMID: 21853288

8

Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population.

Lv Z, Guo J, Sun Q, Li K, Yu R, Tian J, Yan X, Tang B. Lv Z, et al. Parkinsonism Relat Disord. 2012 Jun;18(5):641-4. doi: 10.1016/j.parkreldis.2012.02.015. Epub 2012 Mar 27. Parkinsonism Relat Disord. 2012. PMID: 22459563

9

Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease.

Tian JY, Guo JF, Wang L, Sun QY, Yao LY, Luo LZ, Shi CH, Hu YC, Yan XX, Tang BS. Tian JY, et al. Among authors: sun qy. Neurosci Lett. 2012 May 16;516(2):207-11. doi: 10.1016/j.neulet.2012.03.086. Epub 2012 Apr 5. Neurosci Lett. 2012. PMID: 22503729

10

Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population.

Li K, Tang BS, Yu RL, Lv ZY, Sun QY, Li Q, Xia K, Yan XX, Guo JF. Li K, et al. Among authors: sun qy. Neurosci Lett. 2012 May 23;517(1):56-9. doi: 10.1016/j.neulet.2012.04.024. Epub 2012 Apr 15. Neurosci Lett. 2012. PMID: 22531747

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