|
| 37853106 | Associations of presenting visual acuity with morphological changes on OCT in neovascular age-related macular degeneration: PRECISE Study Report 2. | Eye (Lond) | 2024 |
| 36252678 | Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa. | Am J Ophthalmol | 2023 |
| 37088464 | Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants: Lessons Learned From the ABCA4 Locus. | Lab Invest | 2023 |
| 37284979 | Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. | Mol Diagn Ther | 2023 |
| 37109349 | A Multi-Modal AI-Driven Cohort Selection Tool to Predict Suboptimal Non-Responders to Aflibercept Loading-Phase for Neovascular Age-Related Macular Degeneration: PRECISE Study Report 1. | J Clin Med | 2023 |
| 36819107 | Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis. | Front Cell Dev Biol | 2023 |
| 36746120 | Associations with Non-Persistence with Intra-Vitreal Therapy for Neovascular Age-Related Macular Degeneration at 24 Months. | Ophthalmologica | 2023 |
| 36934458 | Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategies. | Mol Genet Genomic Med | 2023 |
| 36672932 | Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. | Genes (Basel) | 2023 |
| 36729561 | UNITED KINGDOM DATABASE STUDY OF INTRAVITREAL DEXAMETHASONE IMPLANT (OZURDEX) FOR MACULAR EDEMA RELATED TO RETINAL VEIN OCCLUSION. | Retina | 2023 |
| 35934205 | Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene. | Ophthalmology | 2023 |
| 35314386 | The Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D Gene. | Ophthalmol Retina | 2022 |
| 35693422 | Novel homozygous mutations in the transcription factor <i>NRL</i> cause non-syndromic retinitis pigmentosa. | Mol Vis | 2022 |
| 35693420 | Novel <i>SIX6</i> mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. | Mol Vis | 2022 |
| 36161843 | Associations with visual acuity outcomes after 12 months of treatment in 9401 eyes with neovascular AMD. | BMJ Open Ophthalmol | 2022 |
| 32415187 | Changes in venous calibre during intra-vitreal therapy for central retinal vein occlusion. | Eye (Lond) | 2021 |
| 34766849 | Prevalence of Dark without Pressure and Angioid Streaks in Sickle Cell Disease. | Ophthalmic Surg Lasers Imaging Retina | 2021 |
| 33120391 | Sickle Cell Maculopathy: Prevalence, Associations and Impact on Visual Acuity. | Ophthalmologica | 2021 |
| 32144084 | Progression from Early/Intermediate to Advanced Forms of Age-Related Macular Degeneration in a Large UK Cohort: Rates and Risk Factors. | Ophthalmol Retina | 2020 |
| 32821523 | Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular Degeneration. | Transl Vis Sci Technol | 2020 |
| 30676615 | Secondary End Points in the RIVAL Study. | JAMA Ophthalmol | 2019 |
| 31416764 | Direct Ophthalmic Healthcare Resource Use among Patients with Geographic Atrophy in a Large Cohort from the United Kingdom. | Ophthalmol Retina | 2019 |
| 31058429 | Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene. | Hum Mutat | 2019 |
| 30825406 | Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders. | Hum Mutat | 2019 |
| 30377383 | Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. | Genet Med | 2019 |
| 30607024 | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. | Genet Med | 2019 |
| 28929832 | CNGB3 mutations cause severe rod dysfunction. | Ophthalmic Genet | 2018 |
| 30255790 | Rare retinal complications of bone marrow transplantation (BMT): a case report. | BMC Ophthalmol | 2018 |
| 29852030 | Association of Genetic Variants With Response to Anti-Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration. | JAMA Ophthalmol | 2018 |
| 30315276 | Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa. | Nat Commun | 2018 |
| 28406859 | VISUAL ACUITY IMPROVEMENT WHEN SWITCHING FROM RANIBIZUMAB TO AFLIBERCEPT IS NOT SUSTAINED. | Retina | 2018 |
| 29391521 | A clinical and molecular characterisation of CRB1-associated maculopathy. | Eur J Hum Genet | 2018 |
| 29657974 | Monocular and binocular visual impairment in the UK Biobank study: prevalence, associations and diagnoses. | BMJ Open Ophthalmol | 2018 |
| 29366564 | Characterizing Disease Burden and Progression of Geographic Atrophy Secondary to Age-Related Macular Degeneration. | Ophthalmology | 2018 |
| 29320387 | Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes. | Genes (Basel) | 2018 |
| 27965262 | The United Kingdom Diabetic Retinopathy Electronic Medical Record Users Group, Report 1: baseline characteristics and visual acuity outcomes in eyes treated with intravitreal injections of ranibizumab for diabetic macular oedema. | Br J Ophthalmol | 2017 |
| 28487377 | The UK Diabetic Retinopathy Electronic Medical Record (UK DR EMR) Users Group, Report 2: real-world data for the impact of cataract surgery on diabetic macular oedema. | Br J Ophthalmol | 2017 |
| 28253385 | Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy. | JAMA Ophthalmol | 2017 |
| 28478396 | UK AMD/DR EMR REPORT IX: comparative effectiveness of predominantly as needed (PRN) ranibizumab versus continuous aflibercept in UK clinical practice. | Br J Ophthalmol | 2017 |
| 29354705 | Vitreoretinal interface abnormalities in middle-aged adults with visual impairment in the UK Biobank study: prevalence, impact on visual acuity and associations. | BMJ Open Ophthalmol | 2017 |
| 28572062 | The United Kingdom Diabetic Retinopathy Electronic Medical Record Users Group: Report 3: Baseline Retinopathy and Clinical Features Predict Progression of Diabetic Retinopathy. | Am J Ophthalmol | 2017 |
| 28913923 | An Induced Pluripotent Stem Cell Patient Specific Model of Complement Factor H (Y402H) Polymorphism Displays Characteristic Features of Age-Related Macular Degeneration and Indicates a Beneficial Role for UV Light Exposure. | Stem Cells | 2017 |
| 28643799 | Appropriateness of quality standards for meaningful intercentre comparisons of aflibercept service provision for neovascular age-related macular degeneration. | Eye (Lond) | 2017 |
| 28586915 | Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. | Invest Ophthalmol Vis Sci | 2017 |
| 26173461 | The association between systolic blood pressure, ocular perfusion pressure and subfoveal choroidal thickness in normal individuals. | Acta Ophthalmol | 2016 |
| 28173158 | Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility. | Hum Mol Genet | 2016 |
| 26578446 | First-Year Visual Acuity Outcomes of Providing Aflibercept According to the VIEW Study Protocol for Age-Related Macular Degeneration. | Ophthalmology | 2016 |
| 27615601 | UK Age-Related Macular Degeneration Electronic Medical Record System (AMD EMR) Users Group Report IV: Incidence of Blindness and Sight Impairment in Ranibizumab-Treated Patients. | Ophthalmology | 2016 |
| 27173377 | Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes. | Prog Retin Eye Res | 2016 |
| 27419839 | The UK Neovascular AMD Database Report 3: inter-centre variation in visual acuity outcomes and establishing real-world measures of care. | Eye (Lond) | 2016 |