Ni W - Search Results

1

The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful.

Zhou Q, Ni W, Dong Y, Wang N, Gan SR, Wu ZY. Zhou Q, et al. Among authors: ni w. PLoS One. 2014 Nov 4;9(11):e111356. doi: 10.1371/journal.pone.0111356. eCollection 2014. PLoS One. 2014. PMID: 25369462 Free PMC article.

2

Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis.

Lu HP, Gan SR, Chen S, Li HF, Liu ZJ, Ni W, Wang N, Wu ZY. Lu HP, et al. Among authors: ni w. Neurobiol Aging. 2015 Mar;36(3):1603.e11-4. doi: 10.1016/j.neurobiolaging.2014.10.015. Epub 2014 Oct 16. Neurobiol Aging. 2015. PMID: 25457026

3

Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy.

Ni W, Chen S, Qiao K, Wang N, Wu ZY. Ni W, et al. PLoS One. 2015 Mar 26;10(3):e0122279. doi: 10.1371/journal.pone.0122279. eCollection 2015. PLoS One. 2015. PMID: 25811990 Free PMC article.

4

Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population.

Gan SR, Ni W, Dong Y, Wang N, Wu ZY. Gan SR, et al. Among authors: ni w. PLoS One. 2015 Aug 12;10(8):e0134405. doi: 10.1371/journal.pone.0134405. eCollection 2015. PLoS One. 2015. PMID: 26266536 Free PMC article.

5

Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients.

Chen S, Gan SR, Cai PP, Ni W, Zhou Q, Dong Y, Wang N, Wu ZY. Chen S, et al. Among authors: ni w. CNS Neurosci Ther. 2016 Jan;22(1):38-42. doi: 10.1111/cns.12443. Epub 2015 Sep 4. CNS Neurosci Ther. 2016. PMID: 26336829 Free PMC article.

6

Effect of Apolipoprotein E Genotypes on Huntington's Disease Phenotypes in a Han Chinese Population.

Li XY, Zhang YB, Xu M, Cheng HR, Dong Y, Ni W, Li HL, Wu ZY. Li XY, et al. Among authors: ni w. Neurosci Bull. 2019 Aug;35(4):756-762. doi: 10.1007/s12264-019-00360-1. Epub 2019 Mar 18. Neurosci Bull. 2019. PMID: 30887245 Free PMC article.

7

Genotype-phenotype correlation in 667 Chinese families with spinocerebellar ataxia type 3.

Du YC, Dong Y, Cheng HL, Li QF, Yang L, Shao YR, Ma Y, Ni W, Gan SR, Wu ZY. Du YC, et al. Among authors: ni w. Parkinsonism Relat Disord. 2020 Sep;78:116-121. doi: 10.1016/j.parkreldis.2020.07.024. Epub 2020 Aug 4. Parkinsonism Relat Disord. 2020. PMID: 32814229

8

Chinese patients with spinocerebellar ataxia type 3 presenting with rare clinical symptoms.

Dong Y, Sun YM, Ni W, Gan SR, Wu ZY. Dong Y, et al. Among authors: ni w. J Neurol Sci. 2013 Jan 15;324(1-2):167-71. doi: 10.1016/j.jns.2012.10.030. Epub 2012 Nov 20. J Neurol Sci. 2013. PMID: 23174085

9

PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia.

Li HF, Ni W, Xiong ZQ, Xu J, Wu ZY. Li HF, et al. Among authors: ni w. CNS Neurosci Ther. 2013 Jan;19(1):61-5. doi: 10.1111/cns.12034. Epub 2012 Nov 24. CNS Neurosci Ther. 2013. PMID: 23176561 Free PMC article.

10

A variant within FGF1 is associated with Alzheimer's disease in the Han Chinese population.

Tao QQ, Sun YM, Liu ZJ, Ni W, Yang P, Li HL, Lu SJ, Wu ZY. Tao QQ, et al. Among authors: ni w. Am J Med Genet B Neuropsychiatr Genet. 2014 Mar;165B(2):131-6. doi: 10.1002/ajmg.b.32205. Epub 2014 Jan 24. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24464990

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