Publications by authors named "Linliu Peng"

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Peripheral Inflammation Profile of Cerebellar Ataxia.
Cuiling Tang, Qi Deng, Xinrong Yuan, Ziyan Ding, Jian Hu, Linliu Peng

Curr Neuropharmacol· August 2025

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Extending the Mutational Spectrum of SYNE1 Ataxia in Chinese Patients.
Xin Huang, Zhao Chen, Qian Jiang, Panyan Liu, Yiqing Gong, Linliu Peng

Cerebellum· August 2025

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Alterations of the skin microbiome in multiple system atrophy: a pilot study.
Daji Chen, Lang Sun, Linlin Wan, Zhao Chen, LinLiu Peng, Jinzi Peng

NPJ Parkinsons Dis· August 2025

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Decreased Peripheral Blood Lymphocytes in Spinocerebellar Ataxia Type 3 Correlate with Disease Severity.
Qi Deng, Cuiling Tang, Zhao Chen, Xinrong Yuan, Ziyan Ding, Linliu Peng

Mov Disord· July 2025

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Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxia.
Hongyu Yuan, Zhao Chen, Linlin Wan, Linliu Peng, Zhe Long

Gene· July 2025

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A meta-analysis of survival and prognostic factors in multiple system atrophy.
Xiao Dong, Daji Chen, Linlin Wan, Linliu Peng, Zhao Chen

J Neurol· June 2025

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The Status and Future Directions of Treatments for Polyglutamine Spinocerebellar Ataxia: A Bibliometric and Visual Analysis.
Siyu Ding, Linliu Peng, Zhao Chen, Mengyuan Dong, Cuiling Tang

Curr Neuropharmacol· May 2025

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Genetic Analysis of GCA Repeats in the GLS Gene: Implications for Undiagnosed Ataxia and Spinocerebellar Ataxia 3 in Mainland China.
Lijing Lei, Linliu Peng, Linlin Wan, Zhao Chen, Chunrong Wang, Huirong Peng

Mov Disord· February 2025

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The genetic landscape and phenotypic spectrum of GAA-FGF14 ataxia in China: a large cohort study.
Riwei Ouyang, Linlin Wan, David Pellerin, Zhe Long, Jian Hu, Linliu Peng, Huirong Peng

EBioMedicine· April 2024

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Peripheral Inflammatory and Immune Landscape in Multiple System Atrophy: A Cross-Sectional Study.
Xinrong Yuan, Linlin Wan, Zhao Chen, Zhe Long, Daji Chen, Linliu Peng

Mov Disord· February 2024

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Efficacy of cerebellar transcranial magnetic stimulation in spinocerebellar ataxia type 3: a randomized, single-blinded, controlled trial.
Yuting Shi, Guangdong Zou, Zhao Chen, Linlin Wan, Linliu Peng, Huirong Peng

J Neurol· November 2023

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No Correlation between Plasma GPNMB Levels and Multiple System Atrophy in Chinese Cohorts.
Linlin Wan, You Fu, Zhao Chen, Zhe Long, Daji Chen, Linliu Peng

Mov Disord· October 2023

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Diagnostic and prognostic performance of plasma neurofilament light chain in multiple system atrophy: a cross-sectional and longitudinal study.
Linliu Peng, Linlin Wan, Mingjie Liu, Zhe Long, Daji Chen, Huirong Peng

J Neurol· September 2023

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Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography.
Zhao Chen, Guang Liao, Na Wan, Zhiyou He, Daji Chen, Linliu Peng, Huirong Peng

Mov Disord· June 2023

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Characterization of the central motor conduction time in a large cohort of spinocerebellar ataxia type 3 patients.
Yuting Shi, Linliu Peng, Guangdong Zou, Zhao Chen, Linlin Wan, Huirong Peng

Parkinsonism Relat Disord· November 2022

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Explainable artificial intelligence based on feature optimization for age at onset prediction of spinocerebellar ataxia type 3.
Danlei Ru, Jinchen Li, Ouyi Xie, Linliu Peng, Hong Jiang

Front Neuroinform· August 2022

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The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study.
Yun Peng, Linliu Peng, Zhao Chen, Huirong Peng, Puzhi Wang

Front Aging Neurosci· July 2022

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Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First Time.
Yue Xie, Zhao Chen, Zhe Long, Rui-Ting Chen, Yi-Zheng Jiang, Lin-Liu Peng, Hui-Rong Peng

Cerebellum· June 2022

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The progression rate of spinocerebellar ataxia type 3 varies with disease stage.
Linliu Peng, Yun Peng, Zhao Chen, Chunrong Wang, Zhe Long, Huirong Peng

J Transl Med· May 2022

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Blood Neurofilament Light Chain in Genetic Ataxia: A Meta-Analysis.
Linliu Peng, Shang Wang, Zhao Chen, Yun Peng, Chunrong Wang, Huirong Peng

Mov Disord· January 2022

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CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells.
Lang He, Shang Wang, Linliu Peng, Huifang Zhao, Shuai Li, Yun Peng, Huirong Peng

Transl Psychiatry· September 2021

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Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.
Na Wan, Zhao Chen, Linlin Wan, Hongyu Yuan, Zhichao Tang, Yun Peng, Linliu Peng, Huirong Peng

Parkinsonism Relat Disord· August 2021

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New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3.
Linliu Peng, Zhao Chen, Zhe Long, Mingjie Liu, Lijing Lei, Huirong Peng, Yun Peng

Neurology· June 2021

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Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line (CSUXHi005-A) from human urine epithelial cells.
Lang He, Xiaobo Han, Huifang Zhao, Shuai Li, Zhao Chen, Linliu Peng

Stem Cell Res· May 2021

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Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy.
Lang He, Zhao Chen, Linliu Peng, Beisha Tang, Hong Jiang

Exp Neurol· March 2021

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