Chonglin Chen

State Key Laboratory Of Ophthalmology, Guangdong Provincial Key Laboratory Of Ophthalmology And Visual Science
Guangzhou, 510060, China

Last Updated: 09/26/2026

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Found 23 publications

Ocular Phenotypes and Novel SLC45A2 Variants in Patients with Oculocutaneous Albinism Type 4.

Ocular Phenotypes and Novel SLC45A2 Variants in Patients with Oculocutaneous Albinism Type 4.

Journal: Genes

Published: July 12, 2026

Clinical Manifestations and Genetic Spectrum of Oculocutaneous Albinism Type 2 in Chinese Patients.

Clinical Manifestations and Genetic Spectrum of Oculocutaneous Albinism Type 2 in Chinese Patients.

Journal: Genes

Published: March 18, 2026

VISUAL AND ANATOMIC OUTCOMES OF VITRECTOMY FOR MYOPIC MACULOSCHISIS WITH AND WITHOUT MACULAR DETACHMENT: A Case-Control Study.

VISUAL AND ANATOMIC OUTCOMES OF VITRECTOMY FOR MYOPIC MACULOSCHISIS WITH AND WITHOUT MACULAR DETACHMENT: A Case-Control Study.

Journal: Retina (Philadelphia, Pa.)

Published: September 22, 2025

TYR mutation in a Chinese population with oculocutaneous albinism: Molecular characteristics and ophthalmic manifestations.

TYR mutation in a Chinese population with oculocutaneous albinism: Molecular characteristics and ophthalmic manifestations.

Journal: Experimental eye research

Published: August 22, 2023

Improvement in health-related quality of life with Botulinum toxin A injection in acquired superior oblique palsy.

Improvement in health-related quality of life with Botulinum toxin A injection in acquired superior oblique palsy.

Journal: Frontiers in medicine

Published: April 01, 2023

Clinical Features and Novel Genetic Variants Associated with Hermansky-Pudlak Syndrome.

Clinical Features and Novel Genetic Variants Associated with Hermansky-Pudlak Syndrome.

Journal: Genes

Published: June 23, 2022

Clinical features of ocular toxocariasis: a comparison between ultra-wide-field and conventional camera imaging.

Clinical features of ocular toxocariasis: a comparison between ultra-wide-field and conventional camera imaging.

Journal: Eye (London, England)

Published: July 28, 2020

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Journal: Genes

Published: July 20, 2020

Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment.

Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment.

Journal: Genes

Published: June 06, 2020

New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuroma.

New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuroma.

Journal: BMC ophthalmology

Published: June 02, 2020

Novel Compound Heterozygous BBS2 and Homozygous MKKS Variants Detected in Chinese Families with Bardet-Biedl Syndrome.

Novel Compound Heterozygous BBS2 and Homozygous MKKS Variants Detected in Chinese Families with Bardet-Biedl Syndrome.

Journal: Journal of ophthalmology

Published: May 23, 2020

Clinical manifestation and genetic analysis in Chinese early onset X-linked retinoschisis.

Clinical manifestation and genetic analysis in Chinese early onset X-linked retinoschisis.

Journal: Molecular genetics & genomic medicine

Published: March 27, 2020

Showing 1-12 of 23

Last Updated: 09/26/2026