Publications by authors named "Chenxin Ying"

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Genetic and Phenotypic Overlap Between Primary Brain Calcification and Paroxysmal Dyskinesia.
Dehao Yang, Yangguang Lu, Honghao Huang, Zihan Jiang, Yiran Bu, Chenxin Ying

Mov Disord· November 2025

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A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's Disease.
Xiaosheng Zheng, Zhidong Cen, Xinhui Chen, Fan Zhang, Chenxin Ying

Mov Disord· November 2025

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Novel SPR mutation in first Chinese patient with sepiapterin reductase deficiency: urinary biomarker validation in oldest treated case.
Xiaosheng Zheng, Chenxin Ying, Fei Xie, Zhidong Cen, Wei Luo

Neurol Sci· August 2025

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Novel Phenotypes and Deep Intronic Variant Expand TH-Associated Dopa-Responsive Dystonia Spectrum.
Xiaosheng Zheng, Chenxin Ying, Nan Jin, Jinghong Ma, Xinhua Wan

Ann Clin Transl Neurol· May 2025

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Genetic Mutations in Cell Junction Proteins Associated with Brain Calcification.
Dehao Yang, Zihan Jiang, Honghao Huang, Lebo Wang, Chenxin Ying

Mov Disord· March 2025

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Unveiling distinct clinical manifestations of primary familial brain calcifications in Asian and European patients: A study based on 10-year individual-level data.
Dehao Yang, Honghao Huang, Tian Zeng, Lebo Wang, Chenxin Ying

Parkinsonism Relat Disord· March 2025

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Long-read sequencing revealed complex biallelic pentanucleotide repeat expansions in RFC1-related Parkinson's disease.
Peng Liu, Fan Zhang, Xinhui Chen, Xiaosheng Zheng, Miao Chen, Chenxin Ying

NPJ Parkinsons Dis· January 2025

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A Homozygous Variant in NAA60 Is Associated with Primary Familial Brain Calcification.
Xinhui Chen, Yihua Shi, Feng Fu, Lebo Wang, Hongying Yu, Chenxin Ying

Mov Disord· December 2024

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Neurofilament light chain as a mediator between LRRK2 mutation and dementia in Parkinson's disease.
Dehao Yang, Haobo Xie, Sheng Wu, Chenxin Ying, Yiqun Chen, Yaoying Ge

NPJ Parkinsons Dis· September 2023

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