Yao LY - Search Results

1

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. 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

2

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. Among authors: yao ly. Mov Disord. 2010 Jun 15;25(8):1005-11. doi: 10.1002/mds.23009. Mov Disord. 2010. PMID: 20131388

3

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: yao ly. 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

4

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: yao ly. 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

5

Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China.

Sun QY, Guo JF, Han WW, Zuo X, Wang L, Yao LY, Pan Q, Xia K, Yan XX, Tang BS. Sun QY, et al. Among authors: yao ly. J Clin Neurosci. 2013 Feb;20(2):217-9. doi: 10.1016/j.jocn.2012.01.055. Epub 2012 Nov 11. J Clin Neurosci. 2013. PMID: 23151436

6

Polygenic determinants of Parkinson's disease in a Chinese population.

Guo JF, Li K, Yu RL, Sun QY, Wang L, Yao LY, Hu YC, Lv ZY, Luo LZ, Shen L, Jiang H, Yan XX, Pan Q, Xia K, Tang BS. Guo JF, et al. Among authors: yao ly. Neurobiol Aging. 2015 Apr;36(4):1765.e1-1765.e6. doi: 10.1016/j.neurobiolaging.2014.12.030. Epub 2015 Jan 6. Neurobiol Aging. 2015. PMID: 25623333

7

[NOTCH3 gene mutations in two Chinese families featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].

Sun Q, Li W, Zhou Y, Yi F, Wang J, Hu Y, Yao L, Zhou L, Xu H. Sun Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):816-820. doi: 10.3760/cma.j.issn.1003-9406.2017.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188607 Chinese.

8

Identification of Ser465 as a novel PINK1 autophosphorylation site.

Guo JF, Yao LY, Sun QY, Cui YT, Yang Y, Xu Q, Yan XX, Tang BS. Guo JF, et al. Among authors: yao ly. Transl Neurodegener. 2017 Dec 14;6:34. doi: 10.1186/s40035-017-0103-7. eCollection 2017. Transl Neurodegener. 2017. PMID: 29255601 Free PMC article.

9

[Etiologies and risk factors for young people with intracerebral hemorrhage].

Li W, Sun Q, Duan X, Yi F, Zhou Y, Hu Y, Yao L, Xu H, Zhou L. Li W, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Nov 28;43(11):1246-1250. doi: 10.11817/j.issn.1672-7347.2018.11.013. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018. PMID: 30643071 Free article. Chinese.

10

Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia.

He R, Hu Y, Yao L, Tian Y, Zhou Y, Yi F, Zhou L, Xu H, Sun Q. He R, et al. Prion. 2019 Jan;13(1):116-123. doi: 10.1080/19336896.2019.1617027. Prion. 2019. PMID: 31122137 Free PMC article.

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