Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (266)

« Back to Publications

Geographic atrophy in age-related macular degeneration: phenotypic characterisation for clinical trial consideration.

Borchert GA. et al, (2026), Graefes Arch Clin Exp Ophthalmol

Automated cone photoreceptor detection using synthetic data and deep learning in confocal adaptive optics scanning laser ophthalmoscope images.

Shah M. et al, (2026), Sci Rep, 16

Multimodal imaging and electrophysiological features in bradyopsia associated with homozygous variants (c.895T>C) in Regulator of G-protein Signaling 9 (RGS9).

Borchert GA. et al, (2026), Ophthalmic Genet, 47, 14 - 21

Expanding the Genetic Spectrum in IMPG1 and IMPG2 Retinopathy

Al-Khuzaei S. et al, (2025), Genes, 16, 1474 - 1474

Inherited retinal disease pathway in the UK: a patient perspective and the potential of AI.

Wong W. et al, (2025), Br J Ophthalmol, 109, 1266 - 1271

Stargardt's Connected Research Network Inaugural Meeting: Landscape Review and Horizon Scanning of Stargardt Disease.

Britten-Jones AC. et al, (2025), Transl Vis Sci Technol, 14

Genotype–Phenotype Correlations in PRPH2 Retinopathies: A Comprehensive Analysis of 36 Patients from the Oxford Eye Hospital, UK

Al-Khuzaei S. et al, (2025), Genes, 16, 1016 - 1016

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

Woof W. et al, (2025), medRxiv

Sleep and mood in central serous chorioretinopathy.

Yang Y. et al, (2025), Eye (Lond), 39, 1615 - 1623

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.

Woof WA. et al, (2025), Ophthalmol Sci, 5

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.

Pontikos N. et al, (2025), Nat Mach Intell, 7, 967 - 978

Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases.

Naik G. et al, (2025), Ophthalmol Sci, 5

Real-world six-month outcomes in patients switched to faricimab following partial response to anti-VEGF therapy for neovascular age-related macular degeneration and diabetic macular oedema.

Borchert GA. et al, (2024), Eye (Lond), 38, 3569 - 3577

Expanding the genotypic and phenotypic spectra with a novel variant in the ciliopathy gene, CFAP410, associated with selective cone degeneration.

Borchert GA. et al, (2024), Ophthalmic Genet, 45, 633 - 639

Adaptive optics scanning laser ophthalmoscopy in a heterogenous cohort with Stargardt disease.

Shah M. et al, (2024), Sci Rep, 14

Load More

1
2
3
4
5
6
7
...
»