Wenmin Sun

State Key Laboratory Of Ophthalmology
Guangzhou, China

Last Updated: 09/26/2026

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Found 89 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

Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature Review.

Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature Review.

Journal: Investigative ophthalmology & visual science

Published: January 14, 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

Pigmentation Pattern of Iris and Fundus in 75 Chinese Families With GPR143-Associated Ocular Albinism.

Pigmentation Pattern of Iris and Fundus in 75 Chinese Families With GPR143-Associated Ocular Albinism.

Journal: Investigative ophthalmology & visual science

Published: September 30, 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

Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature Review.

Genetic and Clinical Features of FOXL2-Associated Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Based on 11 Chinese Families and Literature Review.

Journal: American journal of medical genetics. Part A

Published: June 20, 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

Clinical and Genetic Characteristics of 18 Patients from Southeast China with ABCA4-Associated Stargardt Disease.

Clinical and Genetic Characteristics of 18 Patients from Southeast China with ABCA4-Associated Stargardt Disease.

Journal: International journal of molecular sciences

Published: February 15, 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

Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes.

Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes.

Journal: Progress in retinal and eye research

Published: January 06, 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

Showing 1-12 of 89

Last Updated: 09/26/2026