Yu-wen Zhao

Changsha, China

Last Updated: 09/26/2026

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Found 13 publications

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

Association of rare PPARGC1A variants with Parkinson's disease risk.

Association of rare PPARGC1A variants with Parkinson's disease risk.

Journal: Journal of human genetics

Published: March 25, 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

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

Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease.

Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: August 18, 2020

Assessment of the association between NUS1 variants and essential tremor.

Assessment of the association between NUS1 variants and essential tremor.

Journal: Neuroscience letters

Published: May 12, 2020

GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.

GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.

Journal: Translational neurodegeneration

Published: April 25, 2020

Coding mutations in NUS1 contribute to Parkinson's disease.

Coding mutations in NUS1 contribute to Parkinson's disease.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: October 24, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026