Xueqing Li

State Key Laboratory Of Ophthalmology, Guangdong Provincial Key Laboratory Of Ophthalmology And Visual Science
Guangzhou, 510623, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

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

Double Hyperautofluorescence Rings as a Sign of CFAP410-related Retinopathy.

Double Hyperautofluorescence Rings as a Sign of CFAP410-related Retinopathy.

Journal: Investigative ophthalmology & visual science

Published: December 28, 2023

Clinical features of patients with mutations in genes for nanophthalmos.

Clinical features of patients with mutations in genes for nanophthalmos.

Journal: The British journal of ophthalmology

Published: November 23, 2023

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

Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod Dystrophy.

Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod Dystrophy.

Journal: Investigative ophthalmology & visual science

Published: August 22, 2022

Truncation mutations in MYRF underlie primary angle closure glaucoma.

Truncation mutations in MYRF underlie primary angle closure glaucoma.

Journal: Human genetics

Published: July 08, 2022

Different Phenotypes Represent Advancing Stages of ABCA4-Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center.

Different Phenotypes Represent Advancing Stages of ABCA4-Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center.

Journal: Investigative ophthalmology & visual science

Published: May 24, 2022

Autosomal Dominant Retinitis Pigmentosa-Associated TOPORS Protein Truncating Variants Are Exclusively Located in the Region of Amino Acid Residues 807 to 867.

Autosomal Dominant Retinitis Pigmentosa-Associated TOPORS Protein Truncating Variants Are Exclusively Located in the Region of Amino Acid Residues 807 to 867.

Journal: Investigative ophthalmology & visual science

Published: May 17, 2022

Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance.

Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance.

Journal: The British journal of ophthalmology

Published: March 23, 2022

Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons.

Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons.

Journal: Experimental eye research

Published: October 14, 2021

Novel BMP4 Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than Microphthalmia.

Novel BMP4 Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than Microphthalmia.

Journal: Frontiers in cell and developmental biology

Published: September 02, 2021

Clinical and genetic features of retinoschisis in 120 families with RS1 mutations.

Clinical and genetic features of retinoschisis in 120 families with RS1 mutations.

Journal: The British journal of ophthalmology

Published: May 19, 2021

Showing 1-12 of 19

Last Updated: 09/26/2026