Feng-juan Gao

NHC Key Laboratory Of Myopia And Related Eye Diseases
Shanghai, China

Last Updated: 09/26/2026

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Found 36 publications

Atypical Fundus in X-Linked Ocular Albinism With GPR143 Variant.

Atypical Fundus in X-Linked Ocular Albinism With GPR143 Variant.

Journal: JAMA ophthalmology

Published: May 21, 2026

An electrochemical sensing platform based on targeted paired binding for biomarker detection in human serum samples.

An electrochemical sensing platform based on targeted paired binding for biomarker detection in human serum samples.

Journal: Biosensors & bioelectronics

Published: March 02, 2026

Bilateral retinal astrocytic hamartomas in retinitis pigmentosa: two case reports and systematic review.

Bilateral retinal astrocytic hamartomas in retinitis pigmentosa: two case reports and systematic review.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: February 04, 2026

Expanding the genetic spectra of gyrate atrophy of the choroid and retina in a Chinese cohort in Yunnan province.

Expanding the genetic spectra of gyrate atrophy of the choroid and retina in a Chinese cohort in Yunnan province.

Journal: Human genomics

Published: April 14, 2025

Deficiency of 2-Oxoglutarate Carrier (Slc25a11) Drives RPE Epithelial-to-Mesenchymal Transition and Exacerbates Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration.

Deficiency of 2-Oxoglutarate Carrier (Slc25a11) Drives RPE Epithelial-to-Mesenchymal Transition and Exacerbates Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration.

Journal: Aging cell

Published: March 20, 2025

Case Report: A family of fluctuating cystoid macular edema caused by MYO7A gene mutations.

Case Report: A family of fluctuating cystoid macular edema caused by MYO7A gene mutations.

Journal: Frontiers in medicine

Published: February 25, 2025

Reliability of clinical impressions and optimal genetic diagnostic strategies of heritable connective tissue disorders with ocular involvement in a large Chinese cohort.

Reliability of clinical impressions and optimal genetic diagnostic strategies of heritable connective tissue disorders with ocular involvement in a large Chinese cohort.

Journal: Human genomics

Published: January 21, 2025

Clinical and mutational signatures of CRB1-associated retinopathies: a multicentre study.

Clinical and mutational signatures of CRB1-associated retinopathies: a multicentre study.

Journal: Journal of medical genetics

Published: August 01, 2024

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

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

Showing 1-12 of 36

Last Updated: 09/26/2026