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.

Publications

A Review of the Ocular Phenotype and Correlation with Genotype in Poretti-Boltshauser Syndrome.

Moon WY. et al, (2025), Medicina (Kaunas), 61

Ozanimod-associated macular edema.

Buckley TMW. et al, (2025), Can J Ophthalmol

Collaborative care for pregnant women with eye conditions.

Ong AY. et al, (2025), Clin Med (Lond)

[Correction: Differential diagnosis of age-related macular degeneration].

Charbel Issa P. et al, (2025), Klin Monbl Augenheilkd, 242

Differential Diagnosis of Age-Related Macular Degeneration.

Charbel Issa P. et al, (2025), Klin Monbl Augenheilkd, 242, 7 - 21

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

Pontikos N. et al, (2025), Nature Machine Intelligence

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

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)

Retinopathy associated with maternally inherited diabetes and deafness.

Suribhatla R. and de Silva SR., (2024), Eye (Lond)

Occlusive retinal vasculitis associated with intravitreal Faricimab injections.

Reichel FF. et al, (2024), J Ophthalmic Inflamm Infect, 14

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, 1 - 7

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom.

Woof W. et al, (2024)

IMPG2-Related Maculopathy.

Birtel J. et al, (2024), Am J Ophthalmol, 258, 32 - 42

Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy.

Borchert GA. et al, (2024), Front Neurosci, 18

Retinograd-AI: An Open-source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Dystrophies

Naik G. et al, (2024)

Visual Acuity by Decade in 139 Males with RPGR-Associated Retinitis Pigmentosa.

De Silva SR. et al, (2024), Ophthalmol Sci, 4

Diabetic retinopathy screening: does one size fit all?

Desai P. and De Silva SR., (2023), Br J Ophthalmol, 107, 1763 - 1764

Genetic Counseling For Predictive Retinal Imaging.

De Silva SR. et al, (2023), JAMA Ophthalmol

Intravitreal anti-vascular endothelial growth factor injections in pregnancy and breastfeeding: a case series and systematic review of the literature.

Ong AY. et al, (2023), Eye (Lond)

CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural History.

Daich Varela M. et al, (2023), Ophthalmology. Retina, 7, 918 - 931

Load More

Include forthcoming?