Jiamin Ouyang

State Key Laboratory Of Ophthalmology
Guangzhou, China

Last Updated: 09/26/2026

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Found 33 publications

Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort.

Clinical and Genetic Characteristics of a Chinese Occult Maculopathy Cohort.

Journal: Translational vision science & technology

Published: March 27, 2026

ARR3 variant-induced cone mosaicism alters cone subtype composition and disrupts phototransduction.

ARR3 variant-induced cone mosaicism alters cone subtype composition and disrupts phototransduction.

Journal: Zoological research

Published: January 06, 2026

Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor Morphology.

Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor Morphology.

Journal: Investigative ophthalmology & visual science

Published: December 11, 2025

Retinitis Pigmentosa-Associated Gene TRIM49 Regulates ULK1-Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium.

Retinitis Pigmentosa-Associated Gene TRIM49 Regulates ULK1-Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: July 02, 2025

Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndrome.

Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndrome.

Journal: Molecular vision

Published: June 20, 2025

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype.

ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype.

Journal: Investigative ophthalmology & visual science

Published: January 30, 2025

The Systemic Genotype-Phenotype Characterization of PAX6-Related Eye Disease in 164 Chinese Families.

The Systemic Genotype-Phenotype Characterization of PAX6-Related Eye Disease in 164 Chinese Families.

Journal: Investigative ophthalmology & visual science

Published: August 30, 2024

Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families.

Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families.

Journal: Investigative ophthalmology & visual science

Published: January 08, 2024

Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner.

Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner.

Journal: International journal of molecular sciences

Published: October 12, 2023

Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia.

Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia.

Journal: Nature communications

Published: June 06, 2023

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.

Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.

Journal: Investigative ophthalmology & visual science

Published: April 25, 2023

The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia.

The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia.

Journal: Investigative ophthalmology & visual science

Published: March 14, 2023

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Last Updated: 09/26/2026