Qi-ying Sun

Changsha, China

Last Updated: 09/26/2026

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Found 33 publications

Typical Clinical Phenotypes and Genotype in a Chinese Family With Congenital Fibrosis of the Extraocular Muscles Type 1.

Typical Clinical Phenotypes and Genotype in a Chinese Family With Congenital Fibrosis of the Extraocular Muscles Type 1.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: September 04, 2024

Biallelic Variants in EPG5 Gene Are Associated with Parkinson's Disease.

Biallelic Variants in EPG5 Gene Are Associated with Parkinson's Disease.

Journal: Annals of neurology

Published: July 03, 2024

Analysis of GIPC1 CGG repeat expansions in essential tremor.

Analysis of GIPC1 CGG repeat expansions in essential tremor.

Journal: Parkinsonism & related disorders

Published: May 20, 2022

The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.

The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.

Journal: Frontiers in aging neuroscience

Published: July 29, 2021

PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment.

PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment.

Journal: Neurobiology of aging

Published: May 24, 2021

PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.

PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.

Journal: Brain : a journal of neurology

Published: April 01, 2021

Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study.

Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study.

Journal: Frontiers in neurology

Published: March 22, 2021

Evaluating the role of ARSA in Chinese patients with Parkinson's disease.

Evaluating the role of ARSA in Chinese patients with Parkinson's disease.

Journal: Neurobiology of aging

Published: February 24, 2021

UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.

UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.

Journal: Brain : a journal of neurology

Published: December 30, 2020

Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease.

Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease.

Journal: Neurobiology of aging

Published: December 03, 2020

Reply: Assessing the NOTCH2NLC GGC expansion in essential tremor patients from eastern China.

Reply: Assessing the NOTCH2NLC GGC expansion in essential tremor patients from eastern China.

Journal: Brain : a journal of neurology

Published: November 17, 2020

Reply: Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

Reply: Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

Journal: Brain : a journal of neurology

Published: November 04, 2020

Showing 1-12 of 33

Last Updated: 09/26/2026