Chong Cui
Shanghai, China
Last Updated: 09/26/2026
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Found 20 publications
Author Correction: A base editor for the long-term restoration of auditory function in mice with recessive profound deafness.
Journal: Nature biomedical engineering
Published: September 07, 2026
Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: December 18, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Journal: Med (New York, N.Y.)
Published: July 22, 2025
Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness.
Journal: JAMA neurology
Published: July 21, 2025
Clinical gene therapy restores hearing: a paradigm shift.
Journal: Trends in molecular medicine
Published: May 18, 2025
From muscle to brain: the mediating effect of vitamin D in the relationship between muscle loss and cognitive function in Alzheimer's disease.
Journal: Frontiers in aging neuroscience
Published: May 18, 2025
Association of magnetic resonance imaging glymphatic function with gray matter volume loss and cognitive impairment in Alzheimer's disease: a diffusion tensor image analysis along the perivascular space (DTI-ALPS) study.
Journal: Quantitative imaging in medicine and surgery
Published: January 12, 2025
Efficient generation of all ESC-derived mice carrying a homozygous lethal mutation through eight-cell embryo injection.
Journal: Science China. Life sciences
Published: September 22, 2024
Bilateral gene therapy in children with autosomal recessive deafness 9: single-arm trial results.
Journal: Nature medicine
Published: December 15, 2023
A base editor for the long-term restoration of auditory function in mice with recessive profound deafness.
Journal: Nature biomedical engineering
Published: December 08, 2023
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial.
Journal: Lancet (London, England)
Published: November 08, 2023
The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice.
Journal: Cellular and molecular life sciences : CMLS
Published: December 27, 2022
Last Updated: 09/26/2026