Jihong Wu

Shanghai, China

Last Updated: 09/26/2026

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Found 12 publications

Tissue-specific gene dosage disruption is a key feature and pathogenic mechanism of structural variants in the human genome.

Tissue-specific gene dosage disruption is a key feature and pathogenic mechanism of structural variants in the human genome.

Journal: Genome medicine

Published: September 17, 2025

Genotype-specific retinal and choroidal perfusion patterns in inherited retinal diseases: an SS-OCTA analysis.

Genotype-specific retinal and choroidal perfusion patterns in inherited retinal diseases: an SS-OCTA analysis.

Journal: International journal of retina and vitreous

Published: April 27, 2025

The X-Age Project to construct a Chinese aging clock.

The X-Age Project to construct a Chinese aging clock.

Journal: Nature aging

Published: January 13, 2025

Longitudinal scRNA-seq of retinal organoids derived from Stargardt disease patient with ABCA4 mutation.

Longitudinal scRNA-seq of retinal organoids derived from Stargardt disease patient with ABCA4 mutation.

Journal: Scientific data

Published: January 13, 2025

Single-Cell Transcriptomic Dataset of RPGR-associated Retinitis Pigmentosa Patient-Derived Retinal Organoids.

Single-Cell Transcriptomic Dataset of RPGR-associated Retinitis Pigmentosa Patient-Derived Retinal Organoids.

Journal: Scientific data

Published: July 23, 2024

From onset to blindness: a comprehensive analysis of RPGR-associated X-linked retinopathy in a large cohort in China.

From onset to blindness: a comprehensive analysis of RPGR-associated X-linked retinopathy in a large cohort in China.

Journal: Journal of medical genetics

Published: April 29, 2024

Neuroprotective effects of apigenin on retinal ganglion cells in ischemia/reperfusion: modulating mitochondrial dynamics in in vivo and in vitro models.

Neuroprotective effects of apigenin on retinal ganglion cells in ischemia/reperfusion: modulating mitochondrial dynamics in in vivo and in vitro models.

Journal: Journal of translational medicine

Published: December 12, 2023

Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants.

Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants.

Journal: NPJ genomic medicine

Published: May 29, 2023

TRPV4-induced Müller cell gliosis and TNF-α elevation-mediated retinal ganglion cell apoptosis in glaucomatous rats via JAK2/STAT3/NF-κB pathway.

TRPV4-induced Müller cell gliosis and TNF-α elevation-mediated retinal ganglion cell apoptosis in glaucomatous rats via JAK2/STAT3/NF-κB pathway.

Journal: Journal of neuroinflammation

Published: May 07, 2021

Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy.

Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy.

Journal: The British journal of ophthalmology

Published: May 31, 2019

Activation of 5-HT1A Receptors Promotes Retinal Ganglion Cell Function by Inhibiting the cAMP-PKA Pathway to Modulate Presynaptic GABA Release in Chronic Glaucoma.

Activation of 5-HT1A Receptors Promotes Retinal Ganglion Cell Function by Inhibiting the cAMP-PKA Pathway to Modulate Presynaptic GABA Release in Chronic Glaucoma.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: July 05, 2018

Alpha7 nicotinic acetylcholine receptor agonist promotes retinal ganglion cell function via modulating GABAergic presynaptic activity in a chronic glaucomatous model.

Alpha7 nicotinic acetylcholine receptor agonist promotes retinal ganglion cell function via modulating GABAergic presynaptic activity in a chronic glaucomatous model.

Journal: Scientific reports

Published: December 12, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026