Chang-yun Liu
Fuzhou, China
Last Updated: 09/26/2026
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Found 15 publications
Clinical and functional characterization of a novel STUB1 mutation in a Chinese spinocerebellar ataxia 48 pedigree.
Journal: Orphanet journal of rare diseases
Published: July 29, 2024
Eomesodermin expression in CD4+T-cells associated with disease progression in amyotrophic lateral sclerosis.
Journal: CNS neuroscience & therapeutics
Published: August 09, 2023
Potential Pleiotropic Genes and Shared Biological Pathways in Epilepsy and Depression Based on GWAS Summary Statistics.
Journal: Computational intelligence and neuroscience
Published: December 28, 2021
Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients.
Journal: Frontiers in neurology
Published: October 06, 2021
Novel Intronic Mutations of TBK1 Promote Aberrant Splicing Modes in Amyotrophic Lateral Sclerosis.
Journal: Frontiers in molecular neuroscience
Published: April 06, 2021
Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.
Journal: Neurobiology of aging
Published: March 22, 2021
Novel Variants in the FIG4 Gene Associated With Chinese Sporadic Amyotrophic Lateral Sclerosis With Slow Progression.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: December 08, 2020
Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: July 29, 2020
Clinical features and genetic characteristics of hereditary diffuse leukoencephalopathy with spheroids due to CSF1R mutation: a case report and literature review.
Journal: Annals of translational medicine
Published: February 15, 2020
Novel mutation in optineurin causing aggressive ALS+/-frontotemporal dementia.
Journal: Annals of clinical and translational neurology
Published: August 09, 2019
Familial flail leg ALS caused by PFN1 mutation.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: June 08, 2019
Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.
Journal: Human mutation
Published: August 16, 2018
Last Updated: 09/26/2026