Shen JY - Search Results

1

Lack of Association Between DNMT3B Polymorphisms and Sporadic Parkinson's Disease in a Han Chinese Population.

Pan H, Shen JY, Du JJ, Cui SS, Liu J, Lin YQ, He YX, Fu Y, Gao C, Li G, Chen SD, Ma JF. Pan H, et al. Among authors: shen jy. Neurosci Bull. 2018 Oct;34(5):867-869. doi: 10.1007/s12264-018-0233-7. Epub 2018 May 14. Neurosci Bull. 2018. PMID: 29761417 Free PMC article. No abstract available.

2

A haplotype of MAP2K5/SKOR1 was associated with essential tremor in Chinese population.

Chen J, Huang P, He Y, Shen J, Du J, Cui S, Cui P, Chen S, Ma J. Chen J, et al. Parkinsonism Relat Disord. 2018 Aug;53:118-119. doi: 10.1016/j.parkreldis.2018.05.017. Epub 2018 May 16. Parkinsonism Relat Disord. 2018. PMID: 29798820 No abstract available.

3

IL1B polymorphism is associated with essential tremor in Chinese population.

Chen J, Huang P, He Y, Shen J, Du J, Cui S, Chen S, Ma J. Chen J, et al. BMC Neurol. 2019 May 15;19(1):99. doi: 10.1186/s12883-019-1331-5. BMC Neurol. 2019. PMID: 31092216 Free PMC article.

4

Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease.

He YC, Huang P, Li QQ, Sun Q, Li DH, Wang T, Shen JY, Du JJ, Cui SS, Gao C, Fu R, Chen SD. He YC, et al. Among authors: shen jy. Parkinsons Dis. 2017;2017:3217474. doi: 10.1155/2017/3217474. Epub 2017 Jan 24. Parkinsons Dis. 2017. PMID: 28243480 Free PMC article.

5

Clinical correlates of decreased plasma coenzyme Q10 levels in patients with multiple system atrophy.

Du J, Wang T, Huang P, Cui S, Gao C, Lin Y, Fu R, Shen J, He Y, Tan Y, Chen S. Du J, et al. Parkinsonism Relat Disord. 2018 Dec;57:58-62. doi: 10.1016/j.parkreldis.2018.07.017. Epub 2018 Jul 26. Parkinsonism Relat Disord. 2018. PMID: 30093363

6

TMEM230 stop codon mutation is rare in parkinson's disease and essential tremor in eastern China.

He YC, Huang P, Li QQ, Sun Q, Li DH, Wang T, Shen JY, Chen SD. He YC, et al. Among authors: shen jy. Mov Disord. 2017 Feb;32(2):301-302. doi: 10.1002/mds.26875. Epub 2016 Nov 21. Mov Disord. 2017. PMID: 27869322 No abstract available.

7

Novel ATM mutations with ataxia-telangiectasia.

Liu XL, Wang T, Huang XJ, Zhou HY, Luan XH, Shen JY, Chen SD, Cao L. Liu XL, et al. Among authors: shen jy. Neurosci Lett. 2016 Jan 12;611:112-5. doi: 10.1016/j.neulet.2015.11.036. Epub 2015 Nov 25. Neurosci Lett. 2016. PMID: 26628246

8

The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia.

Xu Y, Liu X, Shen J, Tian W, Fang R, Li B, Ma J, Cao L, Chen S, Li G, Tang H. Xu Y, et al. Aging Dis. 2018 Aug 1;9(4):696-705. doi: 10.14336/AD.2018.0208. eCollection 2018 Aug. Aging Dis. 2018. PMID: 30090657 Free PMC article.

9

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18.

Tian WT, Shen JY, Liu XL, Wang T, Luan XH, Zhou HY, Chen SD, Huang XJ, Cao L. Tian WT, et al. Among authors: shen jy. Chin Med J (Engl). 2016 Nov 20;129(22):2759-2761. doi: 10.4103/0366-6999.193444. Chin Med J (Engl). 2016. PMID: 27824013 Free PMC article. No abstract available.

10

Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.

Liu XL, Huang XJ, Luan XH, Zhou HY, Wang T, Wang JY, Shen JY, Chen SD, Tang HD, Cao L. Liu XL, et al. Among authors: shen jy. J Neurol Sci. 2015 May 15;352(1-2):105-6. doi: 10.1016/j.jns.2015.02.027. Epub 2015 Feb 20. J Neurol Sci. 2015. PMID: 25847018 No abstract available.

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