Ni W - Search Results

1

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

2

Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system.

Liu ZJ, Li HF, Tan GH, Tao QQ, Ni W, Cheng XW, Xiong ZQ, Wu ZY. Liu ZJ, et al. Among authors: ni w. Neurobiol Aging. 2014 Dec;35(12):2881.e11-2881.e15. doi: 10.1016/j.neurobiolaging.2014.07.003. Epub 2014 Jul 11. Neurobiol Aging. 2014. PMID: 25109764

3

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.

4

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.

5

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.

6

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.

7

Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencing.

Li HF, Liu ZJ, Dong HL, Xie JJ, Zhao SY, Ni W, Dong Y, Wu ZY. Li HF, et al. Among authors: ni w. Neurobiol Aging. 2017 Jan;49:216.e1-216.e5. doi: 10.1016/j.neurobiolaging.2016.09.018. Epub 2016 Oct 3. Neurobiol Aging. 2017. PMID: 28340953

8

Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study.

Chen S, Ni W, Yin XZ, Liu HQ, Lu C, Zheng QJ, Zhao GX, Xu YF, Wu L, Zhang L, Wang N, Li HF, Wu ZY. Chen S, et al. Among authors: ni w. CNS Neurosci Ther. 2017 Sep;23(9):707-716. doi: 10.1111/cns.12719. Epub 2017 Jul 14. CNS Neurosci Ther. 2017. PMID: 28710804 Free PMC article.

9

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.

Liu ZJ, Lin HX, Wei Q, Zhang QJ, Chen CX, Tao QQ, Liu GL, Ni W, Gitler AD, Li HF, Wu ZY. Liu ZJ, et al. Among authors: ni w. Aging Dis. 2019 Dec 1;10(6):1199-1206. doi: 10.14336/AD.2019.0215. eCollection 2019 Dec. Aging Dis. 2019. PMID: 31788332 Free PMC article.

10

Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.

Wen XD, Li HF, Wang HX, Ni W, Dong Y, Wu ZY. Wen XD, et al. Among authors: ni w. CNS Neurosci Ther. 2015 Aug;21(8):626-30. doi: 10.1111/cns.12412. Epub 2015 Jun 20. CNS Neurosci Ther. 2015. PMID: 26096180 Free PMC article.

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