Fred K. Chen

The Royal Victorian Eye & Ear Hospital — Australia

Medicine · Health Sciences

49h-index9.8kcitations454works2.12yr avg
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Research Topics

Retinal Diseases and Treatments(181), Retinal Development and Disorders(118), Retinal Imaging and Analysis(115), Retinal and Optic Conditions(71), Glaucoma and retinal disorders(69)

Publications449 total

Australasian consensus recommendations on stem cell therapies for managing ocular surface diseases
The Ocular Surface·2026
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement
Nature Communications·2025Open Access
Using RNA-targeting CRISPR-Cas13 and engineered U1 systems to target ABCA4 splice variants in Stargardt disease
Molecular Therapy — Nucleic Acids·2025Open Access
Clinical and Experimental Ophthalmology Goes Paperless in 2026
Clinical and Experimental Ophthalmology·2025Open Access
Phenotypic expansion of retinal abnormalities in <i>folliculin</i> ( <i>FLCN</i> ) variant-related pathology (Birt–Hogg–Dubé syndrome)
Ophthalmic Genetics·2025
Anatomy- versus Sensitivity-Based Loci Preselection in Detecting USH2A-Retinopathy Microperimetric Progression
Ophthalmology Science·2025Open Access
Clinical features and recurrence patterns of pediatric idiopathic orbital inflammatory disease
BMC Ophthalmology·2025Open Access
Internal Limiting Membrane Flap Versus Conventional Peeling for Idiopathic Full Thickness Macular Holes: A Registry Analysis of 2990 Eyes
Clinical and Experimental Ophthalmology·2025Open Access
Peripapillary Retinoschisis: The Expanded Spectrum and New Insights From Multimodal Imaging
American Journal of Ophthalmology·2025Open Access
Inherited Retinal Disease or Age‐Related Macular Degeneration: Predictive Value of Genetic Testing in Macular Disease With Atypical Atrophy
Clinical and Experimental Ophthalmology·2025· 1 cited
#ECR-Poster-08 Phenotypic spectrum of congenital stationary night blindness: associations with foveal hypoplasia
2025Open Access
Genetic and Clinical Investigations of C12orf65 Gene Mutations in Three Chinese Pedigrees
Journal of Neuro-Ophthalmology·2025
Multimodal imaging and electrophysiological features in bradyopsia associated with homozygous variants (c.895T&gt;C) in Regulator of G-protein Signaling 9 ( <i>RGS9</i> )
Ophthalmic Genetics·2025
Self-powered wireless rapid oil quality sensing system based on triboelectric-discharge effect
Nano Energy·2025· 1 cited
Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis Pigmentosa
Investigative Ophthalmology & Visual Science·2025Open Access
Clinical Characteristics of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis in Carriers of a Leber Hereditary Optic Neuropathy Variant
Journal of Neuro-Ophthalmology·2025
Artificial intelligence techniques in inherited retinal diseases: a review
Biomedical Physics & Engineering Express·2025· 1 citedOpen Access
Commentary on ‘Genetic landscape of inherited retinal dystrophies in a Welsh tertiary referral centre’
British Journal of Ophthalmology·2025
Current approaches for Usher syndrome disease models and developing therapies
Frontiers in Cell and Developmental Biology·2025· 1 citedOpen Access
CTNNA1-associated retinal dystrophy: novel multimodal imaging and electrophysiology features
Documenta Ophthalmologica·2025Open Access
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Frequent Co-authors

Lyndon da Cruz(12), Vladimir Stojanović(9), Adnan Tufail(9), Praveen J. Patel(8), Peter Coffey(6), Robyn H. Guymer(4), Caroline R. Baumal(4), David A. Mackey(4), Hei Kam(4), Tsu‐Jae King Liu(4), Dejan Marković(4), Elad Alon(4), Gary S. Rubin(4), Charles C. Wykoff(3), Anantha P. Chandrakasan(3), Usha Chakravarthy(3), Jennifer Arnold(3), Wilson J. Heriot(3), Shane R. Durkin(3), Chi D. Luu(3)