Progress in Retinal and Eye Research

Papers
(The median citation count of Progress in Retinal and Eye Research is 14. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-08-01 to 2025-08-01.)
ArticleCitations
Widefield OCT angiography234
The neuroimmune interface in retinal regeneration233
In vivo application of base and prime editing to treat inherited retinal diseases233
Cell identity changes in ocular surface Epithelia143
Animal models for the evaluation of retinal stem cell therapies138
Immunological aspects of RPE cell transplantation121
Non-vasogenic cystoid maculopathies120
Editorial Board98
Unravelling CYP4V2: Clinical features, genetic insights, pathogenic mechanisms and therapeutic strategies in Bietti crystalline corneoretinal dystrophy97
Structure and function of ABCA4 and its role in the visual cycle and Stargardt macular degeneration96
Corneal stromal repair and regeneration94
Consensus and controversies in the science of endophthalmitis management: Basic research and clinical perspectives93
The impact of sensory neuropathy and inflammation on epithelial wound healing in diabetic corneas92
Mitophagy in the retina: Viewing mitochondrial homeostasis through a new lens88
Central serous chorioretinopathy: An evidence-based treatment guideline88
Editorial Board87
Gene-independent therapeutic interventions to maintain and restore light sensitivity in degenerating photoreceptors87
Squishy matters – Corneal mechanobiology in health and disease80
Photocoagulation for retinal vein occlusion78
Etiopathogenesis of primary acquired nasolacrimal duct obstruction (PANDO)78
Homeostatic plasticity in the retina72
A paradigm shift in retinal detachment repair: The concept of integrity71
Myocilin misfolding and glaucoma: A 20-year update70
The endoplasmic reticulum: Homeostasis and crosstalk in retinal health and disease70
Risk factors, clinical features and treatment of Behçet's disease uveitis70
Cell fate decisions, transcription factors and signaling during early retinal development66
Editorial Board66
Protection against corneal hyperosmolarity with soft-contact-lens wear64
The retinal pigmentation pathway in human albinism: Not so black and white63
Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes63
Multiple gene therapy as a tool for regulating the expression of molecules involved in neovascular age-related macular degeneration63
Corrigendum to “Optical coherence tomography in the management of diabetic macular oedema” [Prog. Retin. Eye Res. 98 (2024) 101220]61
Approaches for corneal endothelium regenerative medicine61
How gut microbiota may impact ocular surface homeostasis and related disorders61
RNA-targeting strategies as a platform for ocular gene therapy61
Cellular component transfer between photoreceptor cells of the retina60
Exploring single-cell RNA sequencing as a decision-making tool in the clinical management of Fuchs’ endothelial corneal dystrophy59
Identification of novel biomarkers for retinopathy of prematurity in preterm infants by use of innovative technologies and artificial intelligence57
Targeting inflammasomes and pyroptosis in retinal diseases—molecular mechanisms and future perspectives57
Rhodopsin, light-sensor of vision56
Optical coherence tomography angiography in diabetic retinopathy56
Editorial Board55
Female carriers of X-linked inherited retinal diseases – Genetics, diagnosis, and potential therapies54
Retinal pigment epithelium 65 kDa protein (RPE65): An update53
Regulation of lens water content: Effects on the physiological optics of the lens53
Genetic therapies and potential therapeutic applications of CRISPR activators in the eye53
Pseudoxanthoma elasticum – Genetics, pathophysiology, and clinical presentation53
The march to harmonized imaging standards for retinal imaging52
The retinal pigment epithelium: Development, injury responses, and regenerative potential in mammalian and non-mammalian systems52
Quantitative approaches in multimodal fundus imaging: State of the art and future perspectives50
Retinal TRP channels: Cell-type-specific regulators of retinal homeostasis and multimodal integration50
Assessment and management of retinopathy of prematurity in the era of anti-vascular endothelial growth factor (VEGF)47
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity43
VEGFR1 signaling in retinal angiogenesis and microinflammation43
Activation of retinal glial cells contributes to the degeneration of ganglion cells in experimental glaucoma43
Bacterial keratitis: identifying the areas of clinical uncertainty43
The immune response in tubercular uveitis and its implications for treatment: From anti-tubercular treatment to host-directed therapies42
Translocator protein (18 kDa) (Tspo) in the retina and implications for ocular diseases41
The role of CFTR in the eye, and the effect of early highly effective modulator treatment for cystic fibrosis on eye health41
Artificial intelligence in ophthalmology: Progress, challenges, and ethical implications40
Editorial Board39
Eye on the horizon: The metabolic landscape of the RPE in aging and disease39
Prospects for the application of Müller glia and their derivatives in retinal regenerative therapies38
Tilted disc syndrome (TDS): New hypotheses for posterior segment complications and their implications in other retinal diseases37
The relationship between intraocular pressure and glaucoma: An evolving concept37
From mouse to human: Accessing the biochemistry of vision in vivo by two-photon excitation36
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, 35
Value proposition of retinal imaging in Alzheimer's disease screening: A review of eight evolving trends34
Potential therapeutic targets for age-related macular degeneration: The nuclear option34
Familial normal tension glaucoma genetics33
Zebrafish and inherited photoreceptor disease: Models and insights33
The multifunctional human ocular melanocortin system31
Syndromic retinitis pigmentosa31
Retinal dystrophins and the retinopathy of Duchenne muscular dystrophy31
The dark and bright sides of retinal G protein-coupled receptor (RGR) in vision and disease30
Healing the cornea: Exploring the therapeutic solutions offered by MSCs and MSC-derived EVs30
Müller cells and astrocytes in tractional macular disorders29
Characterizing Bruch's membrane: State-of-the-art imaging, computational segmentation, and biologic models in retinal disease and health27
Corrigendum to “Glands of Moll: history, current knowledge and their role in ocular surface homeostasis and disease” [Progr. Retin. Eye Res. 106 (2025) 101362]27
Translation of single-cell transcriptomic analysis of uveal melanomas to clinical oncology27
Editorial Board26
Exploring the choroidal vascular labyrinth and its molecular and structural roles in health and disease26
A reinterpretation of critical flicker-frequency (CFF) data reveals key details about light adaptation and normal and abnormal visual processing26
Cellular and subcellular optogenetic approaches towards neuroprotection and vision restoration25
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms25
Editorial Board24
Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapy24
Ocular manifestations of COVID-1924
The two-faced effects of nerves and neuropeptides in corneal diseases24
Latest advances in white spot syndromes: New findings and interpretations24
The AI revolution in glaucoma: Bridging challenges with opportunities23
Pericytes in the optic nerve head23
Trustworthy AI: Closing the gap between development and integration of AI systems in ophthalmic practice21
Müller cells trophism and pathology as the next therapeutic targets for retinal diseases21
Editorial Board21
Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration20
Advances in understanding the molecular structure of retinoschisin while questions remain of biological function20
The physiological and pathophysiological roles of the autophagy lysosomal system in the conventional aqueous humor outflow pathway: More than cellular clean up20
Shining light on CRISPR/Cas9 therapeutics for inherited retinal diseases20
Optical coherence tomography in the management of diabetic macular oedema19
Age and intraocular pressure in murine experimental glaucoma19
Punctate inner choroidopathy: A review of the current diagnostic and therapeutic approaches18
Artificial intelligence in OCT angiography18
Therapy with voretigene neparvovec. How to measure success?18
In vitro and ex vivo models of microbial keratitis: Present and future18
Neuroimmune crosstalk in the cornea: The role of immune cells in corneal nerve maintenance during homeostasis and inflammation18
Corrigendum to “Splicing mutations in inherited retinal diseases” [Prog. Retin. Eye Res. 80 (2021) 100874]18
Posterior corneoscleral limbus: Architecture, stem cells, and clinical implications18
AI in the clinical management of GA: A novel therapeutic universe requires novel tools17
The role of the gut microbiome in eye diseases17
Comparative insights into the role of sex hormones in glaucoma among women and men17
Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities17
Diabetic macular ischaemia- a new therapeutic target?16
Mechanisms of blood-retinal barrier disruption related to intraocular inflammation and malignancy16
Editorial Board15
Toward an internationally accepted standard for reading charts14
IOP and glaucoma damage: The essential role of optic nerve head and retinal mechanosensors14
Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches14
Editorial Board14
Crosslinking with UV-A and riboflavin in progressive keratoconus: From laboratory to clinical practice – Developments over 25 years14
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