Publications by authors named "Min Ting Lin"

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Comprehensive Profiling of Annexins in Neuromuscular Disorders Reveals a Unique Signature in Dysferlinopathy.
Qi-Fang He, Yu-Hua Lin, Ze-Ling Zheng, Ming-Hui Zeng, Xin Lin, Min-Ting Lin, Feng Lin

Eur J Neurol· December 2025

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Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy Patients.
Ru-Ying Yuan, Ya-Fang Chen, Wei Lin, Meng-Cheng Li, Yi-Heng Zeng, Mao-Lin Cui, Yu Lin, Lin-Wei Zhang, En-Lin Dong, Min-Ting Lin

Ann Neurol· October 2025

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Peripheral inflammation in spinocerebellar ataxia type 3: associations with genetic and clinical manifestations.
Jia-Yi Zhang, Qiu-Ni Su, Han Lin, Wei Lin, Mao-Lin Cui, Yi-Lin Jia, Min-Ting Lin

Inflamm Res· October 2025

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Static Posture Instability as a Sensitive Biomarker for Motor Abnormalities in Pre-ataxic Spinocerebellar Ataxia Type 3 Patients.
Mao-Lin Cui, Xia-Hua Liu, Ying Li, Wei Lin, Hao-Ling Xu, Min-Ting Lin

Mov Disord· April 2025

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Fatigue in the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 3.
Zhi-Li Chen, Li-Mei Xiao, Chun Li, Liang-Liang Qiu, Wei Lin, Min-Ting Lin

Eur J Neurol· April 2025

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Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study.
Zhi-Xian Ye, Xuan-Yu Chen, Meng-Cheng Li, Xin-Yuan Chen, Yu-Sen Qiu, Min-Ting Lin

Orphanet J Rare Dis· January 2025

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Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis.
Qi-Jie Zhang, Jie Lin, You-Liang Wang, Long Chen, Ying Ding, Min-Ting Lin, Ling Fang

Brain Pathol· November 2024

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Antisense oligonucleotides enhance SLC20A2 expression and suppress brain calcification in a humanized mouse model.
Miao Zhao, Xuewen Cheng, Lei Chen, Yi-Heng Zeng, Kai-Jun Lin, Yu Lin, Zi-Ling Ye, Min-Ting Lin

Neuron· October 2024

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Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression.
Di Wang, Xin-Yi Liu, Qi-Fang He, Fu-Ze Zheng, Long Chen, Yu-Hua Lin, Xin Lin, Min-Ting Lin, Feng Lin

CNS Neurosci Ther· October 2024

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Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.
Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Min-Ting Lin

Orphanet J Rare Dis· November 2023

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The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy.
Feng Lin, Kang Yang, Min-Ting Lin, Fu-Ze Zheng, Long Chen, Xin Lin

Ann Clin Transl Neurol· March 2023

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Short-term efficacy of repetitive transcranial magnetic stimulation in SCA3: A prospective, randomized, double-blind, sham-controlled study.
Arif Sikandar, Xia-Hua Liu, Hao-Ling Xu, Ying Li, Yun-Qing Lin, Min-Ting Lin

Parkinsonism Relat Disord· January 2023

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CRISPR/Cas9-based genome editing for the modification of multiple duplications that cause Duchenne muscular dystrophy.
Dan-Ni Wang, Zhi-Qiang Wang, Ming Jin, Min-Ting Lin, Ning Wang

Gene Ther· December 2022

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Loss of function of CMPK2 causes mitochondria deficiency and brain calcification.
Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Xiao-Hong Lin, Jingjing Lin, Min-Ting Lin

Cell Discov· November 2022

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GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.
Yi-Heng Zeng, Kang Yang, Gan-Qin Du, Yi-Kun Chen, Chun-Yan Cao, Min-Ting Lin

Ann Neurol· September 2022

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Effect of a Pay-for-Performance Program on Renal Outcomes Among Patients With Early-Stage Chronic Kidney Disease in Taiwan.
Min-Ting Lin, Chien-Ning Hsu, Chien-Te Lee, Shou-Hsia Cheng

Int J Health Policy Manag· August 2022

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Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation.
Kang Yang, Yi-Heng Zeng, Yu-Sen Qiu, Feng Lin, Hai-Zhu Chen, Min-Ting Lin

Acta Neuropathol· June 2022

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CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency.
Xin-Yi Liu, Xue-Jiao Chen, Miao Zhao, Zhi-Qiang Wang, Hai-Zhu Chen, Min-Ting Lin

J Inherit Metab Dis· March 2021

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A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2.
Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Min-Ting Lin

Chin Med J (Engl)· March 2021

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Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings.
Qi-Fu Guo, Zhi-Xian Ye, Liang-Liang Qiu, Xin Lin, Jia-He Lai, Min-Ting Lin, Feng Lin

Chin Med J (Engl)· February 2021

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[Construction of a striatum-specific Slc20a2 gene knockout mice model by CRISPR/Cas9 AAV system].
Min Ting Lin, Lu Lu Lai, Miao Zhao, Bi Wei Lin, Xiang Ping Yao

Yi Chuan· October 2020

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Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients.
Jin-Shan Yang, Hao-Ling Xu, Ping-Ping Chen, Arif Sikandar, Mei-Zhen Qian, Hui-Xia Lin, Min-Ting Lin

Front Neurol· April 2020

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Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice.
Jin-Jing Li, Xiang Lin, Cheng Tang, Ying-Qian Lu, Xinde Hu, Min-Ting Lin, Linyu Shi

Natl Sci Rev· January 2020

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Drug price, dosage and safety: Real-world evidence of oral hypoglycemic agents.
Yu-Shiuan Lin, Min-Ting Lin, Shou-Hsia Cheng

Health Policy· December 2019

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Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes.
Shan Lin, Jia-Bin Zeng, Gui-Xian Zhao, Zhen-Zhen Yang, Hui-Ping Huang, Min-Ting Lin, Ling Fang

Seizure· October 2019

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