Omar A. Mahroo
School Of Life Course Sciences
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 207 publications
Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.
Journal: Investigative ophthalmology & visual science
Published: August 10, 2026
Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.
Journal: Research square
Published: July 17, 2026
MERTK-associated retinal dystrophy: clinical course and imaging.
Journal: Ophthalmic genetics
Published: May 04, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genes.
Journal: Eye (London, England)
Published: April 21, 2026
Correction: ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.
Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: March 26, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental Disorder.
Journal: Investigative ophthalmology & visual science
Published: March 11, 2026
Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathy.
Journal: Acta ophthalmologica
Published: March 02, 2026
ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.
Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: February 03, 2026
A New Gene for Congenital Stationary Night Blindness.
Journal: JAMA ophthalmology
Published: December 04, 2025
Clinical Findings and Molecular Genetics of USH1C-Associated Usher Syndrome.
Journal: JAMA ophthalmology
Published: November 26, 2025
Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype.
Journal: Investigative ophthalmology & visual science
Published: November 13, 2025
Last Updated: 09/26/2026