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New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3.
Peng L, Chen Z, Long Z, Liu M, Lei L, Wang C, Peng H, Shi Y, Peng Y, Deng Q, Wang S, Zou G, Wan L, Yuan H, He L, Xie Y, Tang Z, Wan N, Gong Y, Hou X, Shen L, Xia K, Li J, Chen C, Qiu R, Klockgether T, Tang B, Jiang H. Peng L, et al. Among authors: wang c, wang s. Neurology. 2021 Jun 8;96(23):e2885-e2895. doi: 10.1212/WNL.0000000000012068. Epub 2021 Apr 23. Neurology. 2021. PMID: 33893204
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy.
Wan L, Chen Z, Wan N, Liu M, Xue J, Chen H, Zhang Y, Peng Y, Tang Z, Gong Y, Yuan H, Wang S, Deng Q, Hou X, Wang C, Peng H, Shi Y, Peng L, Lei L, Duan R, Xia K, Qiu R, Shen L, Tang B, Ashizawa T, Jiang H. Wan L, et al. Among authors: wang s, wang c. Ann Neurol. 2020 Dec;88(6):1132-1143. doi: 10.1002/ana.25902. Epub 2020 Oct 3. Ann Neurol. 2020. PMID: 32939785
Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine Learning.
Peng L, Chen Z, Chen T, Lei L, Long Z, Liu M, Deng Q, Yuan H, Zou G, Wan L, Wang C, Peng H, Shi Y, Wang P, Peng Y, Wang S, He L, Xie Y, Tang Z, Wan N, Gong Y, Hou X, Shen L, Xia K, Li J, Chen C, Zhang Z, Qiu R, Tang B, Jiang H. Peng L, et al. Among authors: wang p, wang c, wang s. Mov Disord. 2021 Jan;36(1):216-224. doi: 10.1002/mds.28311. Epub 2020 Sep 29. Mov Disord. 2021. PMID: 32991004
Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.
Wan N, Chen Z, Wan L, Yuan H, Tang Z, Liu M, Peng Y, Peng L, Lei L, Xie Y, Deng Q, Wang S, Wang C, Peng H, Hou X, Shi Y, Long Z, Qiu R, Xia K, Tang B, Jiang H. Wan N, et al. Among authors: wang s, wang c. Parkinsonism Relat Disord. 2021 Aug;89:120-127. doi: 10.1016/j.parkreldis.2021.07.010. Epub 2021 Jul 10. Parkinsonism Relat Disord. 2021. PMID: 34284285
Blood Neurofilament Light Chain in Genetic Ataxia: A Meta-Analysis.
Peng L, Wang S, Chen Z, Peng Y, Wang C, Long Z, Peng H, Shi Y, Hou X, Lei L, Wan L, Liu M, Zou G, Shen L, Xia K, Qiu R, Tang B, Ashizawa T, Klockgether T, Jiang H. Peng L, et al. Among authors: wang s, wang c. Mov Disord. 2022 Jan;37(1):171-181. doi: 10.1002/mds.28783. Epub 2021 Sep 14. Mov Disord. 2022. PMID: 34519102
CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells.
He L, Wang S, Peng L, Zhao H, Li S, Han X, Habimana JD, Chen Z, Wang C, Peng Y, Peng H, Xie Y, Lei L, Deng Q, Wan L, Wan N, Yuan H, Gong Y, Zou G, Li Z, Tang B, Jiang H. He L, et al. Among authors: wang s, wang c. Transl Psychiatry. 2021 Sep 17;11(1):479. doi: 10.1038/s41398-021-01605-2. Transl Psychiatry. 2021. PMID: 34535635 Free PMC article.
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study.
Peng Y, Peng L, Chen Z, Peng H, Wang P, Zhang Y, Li Y, Wang C, Shi Y, Hou X, Long Z, Yuan H, Wan N, Wan L, Xu K, Lei L, Wang S, He L, Xie Y, Gong Y, Deng Q, Zou G, Tang Z, Shen L, Xia K, Qiu R, Klockgether T, Tang B, Jiang H. Peng Y, et al. Among authors: wang p, wang c, wang s. Front Aging Neurosci. 2022 Jul 5;14:917126. doi: 10.3389/fnagi.2022.917126. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35865750 Free PMC article.
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