Fang-yuan Hu

Key Laboratory Of Myopia
Shanghai, China

Last Updated: 09/26/2026

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Found 22 publications

Mutational spectrum in a Chinese cohort with congenital cataracts.

Mutational spectrum in a Chinese cohort with congenital cataracts.

Journal: Molecular genetics & genomic medicine

Published: October 11, 2022

Clinical and Genetic Analysis of Retinitis Pigmentosa with Primary Angle Closure Glaucoma in the Chinese Population.

Clinical and Genetic Analysis of Retinitis Pigmentosa with Primary Angle Closure Glaucoma in the Chinese Population.

Journal: Current eye research

Published: August 04, 2022

Nobiletin protects retinal ganglion cells in models of ocular hypertension in vivo and hypoxia in vitro.

Nobiletin protects retinal ganglion cells in models of ocular hypertension in vivo and hypoxia in vitro.

Journal: Laboratory investigation; a journal of technical methods and pathology

Published: April 13, 2022

Mutation Analysis of the RPGR Gene in a Chinese Cohort.

Mutation Analysis of the RPGR Gene in a Chinese Cohort.

Journal: Frontiers in genetics

Published: January 07, 2022

Regulation of mitophagy by metformin improves the structure and function of retinal ganglion cells following excitotoxicity-induced retinal injury.

Regulation of mitophagy by metformin improves the structure and function of retinal ganglion cells following excitotoxicity-induced retinal injury.

Journal: Experimental eye research

Published: September 17, 2021

Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort.

Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort.

Journal: Eye (London, England)

Published: April 22, 2021

Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing.

Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing.

Journal: Frontiers in bioengineering and biotechnology

Published: May 20, 2020

Novel variants of ABCA4 in Han Chinese families with Stargardt disease.

Novel variants of ABCA4 in Han Chinese families with Stargardt disease.

Journal: BMC medical genetics

Published: March 24, 2020

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China.

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China.

Journal: Acta ophthalmologica

Published: March 20, 2020

Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.

Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.

Journal: The British journal of ophthalmology

Published: January 15, 2020

Panel-based targeted exome sequencing reveals novel candidate susceptibility loci for age-related cataracts in Chinese Cohort.

Panel-based targeted exome sequencing reveals novel candidate susceptibility loci for age-related cataracts in Chinese Cohort.

Journal: Molecular genetics & genomic medicine

Published: December 24, 2019

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population.

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population.

Journal: Orphanet journal of rare diseases

Published: December 09, 2019

Showing 1-12 of 22

Last Updated: 09/26/2026