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Ophthalmic Genetics|January 25, 2026
A novel EYS c.6192-1G>A variant presents ideal base editing therapeutic opportunitiesMaria Kaukonen, Imran H Yusuf, Federica E Poli, et al.Eye (London, England)|May 1, 2018
Microperimetry and optical coherence tomography imaging in the fellow eye of patients with unilateral focal ischaemic glaucomaImran H Yusuf, Jasleen K Jolly, Gokulan Ratnarajan, et al.Journal of Cataract and Refractive Surgery|July 23, 2013
Black-on-black secondary occlusive IOL implantation to alleviate enigmatic light perception through a black IOLImran H Yusuf, Kikkeri S Arun, Paul Rosen, et al.Ophthalmic Genetics|November 23, 2019
A novel splice-site variant in CDH23 in a patient with Usher syndrome type 1Moreno Menghini, Jasmina Cehajic-Kapetanovic, Imran H Yusuf, et al.Ophthalmic Genetics|December 2, 2017
A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxiaImran H Yusuf, Morag E Shanks, Penny Clouston, et al.Eye (London, England)|July 31, 2024
The incidence, monitoring coverage and clinical characteristics of hydroxychloroquine retinopathy in the United KingdomImran H Yusuf, Ruofan C Han, Susan M Downes, et al.Progress in Retinal and Eye Research|January 23, 2022
Retinal cadherins and the retinal cadherinopathies: Current concepts and future directionsImran H Yusuf, Andrew M Garrett, Robert E MacLaren, et al.Klinische Monatsblatter Fur Augenheilkunde|March 30, 2021
Diagnosis of Inherited Retinal DiseasesJohannes Birtel, Imran H Yusuf, Claudia Priglinger, et al.Experimental Eye Research|May 8, 2021
Deep phenotyping of the Cdhr1-/- mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degenerationImran H Yusuf, Michelle E McClements, Robert E MacLaren, et al.Eye (London, England)|November 15, 2022
A nationwide survey of hydroxychloroquine retinopathy presenting to the hospital eye service in the United KingdomImran H Yusuf, Ruofan C Han, Susan M Downes, et al.Pageof 5