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Author Details
Full Name
Jason Charng
Affiliation
University of Western Australia
ORCID
Career Start Year
2011
Papers
48
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37743021
Nonlinear Reduction in Hyperautofluorescent Ring Area in Retinitis Pigmentosa.
Ophthalmol Retina
2024
34815236
Conjunctival ultraviolet autofluorescence area decreases with age and sunglasses use.
Br J Ophthalmol
2023
37594450
Distribution of Axial Length in Australians of Different Age Groups, Ethnicities, and Refractive Errors.
Transl Vis Sci Technol
2023
37619623
Microperimetry Findings in Pentosan Polysulfate Maculopathy.
Ophthalmol Retina
2023
36973718
L-arginine and aged garlic extract for the prevention of migraine: a study protocol for a randomised, double-blind, placebo-controlled, phase-II trial (LARGE trial).
BMC Neurol
2023
36607619
Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation Carriers.
Invest Ophthalmol Vis Sci
2023
35999058
Deep learning: applications in retinal and optic nerve diseases.
Clin Exp Optom
2023
35129629
Localised relative scotoma in cuticular drusen.
Graefes Arch Clin Exp Ophthalmol
2022
35642435
Association between dietary niacin and retinal nerve fibre layer thickness in healthy eyes of different ages.
Clin Exp Ophthalmol
2022
35568370
Prevalence of Toxoplasmic Retinochoroiditis in an Australian Adult Population: A Community-Based Study.
Ophthalmol Retina
2022
36249684
Evaluating Distribution of Foveal Avascular Zone Parameters Corrected by Lateral Magnification and Their Associations with Retinal Thickness.
Ophthalmol Sci
2022
35909098
Correcting magnification error in foveal avascular zone area measurements of optical coherence tomography angiography images with estimated axial length.
Eye Vis (Lond)
2022
32985313
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathy.
Ophthalmic Genet
2021
33624564
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathy.
Ophthalmic Genet
2021
34904999
Short-Term Parafoveal Cone Loss Despite Preserved Ellipsoid Zone in Rod Cone Dystrophy.
Transl Vis Sci Technol
2021
34662343
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
2021
33934469
Increased interdigitation zone visibility on optical coherence tomography following systemic fibroblast growth factor receptor 1-3 tyrosine kinase inhibitor anticancer therapy.
Clin Exp Ophthalmol
2021
34342609
Distribution and Classification of Peripapillary Retinal Nerve Fiber Layer Thickness in Healthy Young Adults.
Transl Vis Sci Technol
2021
34003942
Macular Thickness Profile and Its Association With Best-Corrected Visual Acuity in Healthy Young Adults.
Transl Vis Sci Technol
2021
33047631
Progressive sector retinitis pigmentosa due to c.440G>T mutation in <i>SAG</i> in an Australian family.
Ophthalmic Genet
2021
32217560
Rationale and protocol for the 7- and 8-year longitudinal assessments of eye health in a cohort of young adults in the Raine Study.
BMJ Open
2020
32100917
Western Australia Atropine for the Treatment of Myopia (WA-ATOM) study: Rationale, methodology and participant baseline characteristics.
Clin Exp Ophthalmol
2020
32719476
Age-dependent regional retinal nerve fibre changes in SIX1/SIX6 polymorphism.
Sci Rep
2020
32974081
Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in <i>USH2A</i> Retinopathy.
Transl Vis Sci Technol
2020
32832226
Interpreting MAIA Microperimetry Using Age- and Retinal Loci-Specific Reference Thresholds.
Transl Vis Sci Technol
2020
32627976
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect.
Mol Genet Genomic Med
2020
32931148
Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variants.
Mol Genet Genomic Med
2020
33020556
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease.
Sci Rep
2020
32724127
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations.
Sci Rep
2020
30559420
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect.
Nat Med
2019
31810409
Estimation of heritability and familial correlation in myopia is not affected by past sun exposure.
Ophthalmic Genet
2019
31717845
Autosomal Dominant Retinitis Pigmentosa Due to Class B <i>Rhodopsin</i> Mutations: An Objective Outcome for Future Treatment Trials.
Int J Mol Sci
2019
30285110
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.
Hum Mol Genet
2019
30516820
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion Mutations.
Invest Ophthalmol Vis Sci
2018
30208424
Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 Years.
Invest Ophthalmol Vis Sci
2018
29953849
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG Mutation.
Am J Ophthalmol
2018
28660274
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion Cells.
Invest Ophthalmol Vis Sci
2017
28212877
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations.
Am J Ophthalmol
2017
28174096
Retinal biomarkers provide "insight" into cortical pharmacology and disease.
Pharmacol Ther
2017
28973367
Imaging Lenticular Autofluorescence in Older Subjects.
Invest Ophthalmol Vis Sci
2017
28510626
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene.
Invest Ophthalmol Vis Sci
2017
27309625
Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone Diseases.
Invest Ophthalmol Vis Sci
2016
27798110
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.
Hum Mol Genet
2016
27239335
Retinal Electrophysiology Is a Viable Preclinical Biomarker for Drug Penetrance into the Central Nervous System.
J Ophthalmol
2016
27403810
Implantation and Recording of Wireless Electroretinogram and Visual Evoked Potential in Conscious Rats.
J Vis Exp
2016
23422944
Increased susceptibility to injury in older eyes.
Optom Vis Sci
2013
24069276
Conscious wireless electroretinogram and visual evoked potentials in rats.
PLoS One
2013
22003116
Age-related retinal function changes in albino and pigmented rats.
Invest Ophthalmol Vis Sci
2011
1 - 48 of 48
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Flinders Medical Centre, Flinders University
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The University of Melbourne
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University of California San Diego
Co-authored papers
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Henry Ferreyra
University of California San Diego
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Robyn H Guymer
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Praveen J Patel
NIHR Moorfields Biomedical Research Centre
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