Omar A Mahroo
Overview
Explore the profile of Omar A Mahroo including associated specialties, affiliations and a list of published articles.
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Articles
142
Citations
1002
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0
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Recent Articles
1.
Laich Y, Georgiou M, Fujinami K, Varela M, Fujinami-Yokokawa Y, Hashem S, et al.
Ophthalmol Retina
. 2025 Mar;
PMID: 40086732
Purpose: To analyze the retinal imaging findings and natural history of Best vitelliform macular dystrophy (BVMD). Design: Single-center retrospective, consecutive, observational study. Participants: Patients with a clinical diagnosis of BVMD,...
2.
Kaminska K, Cancellieri F, Quinodoz M, Moye A, Bauwens M, Lin S, et al.
Am J Hum Genet
. 2025 Mar;
PMID: 40081374
Inherited retinal diseases (IRDs) are a genetically heterogeneous group of Mendelian disorders that often lead to progressive vision loss and involve approximately 300 distinct genes. Although variants in these loci...
3.
Wong W, Mahroo O
Clin Exp Ophthalmol
. 2025 Feb;
PMID: 40013354
Phototransduction, the process by which captured photons elicit electrical changes in retinal rod and cone cells, represents the first neuronal step in vision and involves interactions between several highly specialised...
4.
Allon G, Lin S, Robson A, Arno G, Neveu M, Hysi P, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):50.
PMID: 39969478
Purpose: To report findings in GUCA1A-associated retinopathy, a rare autosomal-dominant retinopathy. Methods: Clinical features and investigations from molecularly confirmed patients at a large referral center were analyzed (retrospective cohort study)....
5.
Woof W, de Guimaraes T, Al-Khuzaei S, Varela M, Sen S, Bagga P, et al.
Ophthalmol Sci
. 2025 Feb;
5(2):100652.
PMID: 39896422
Purpose: To quantify relevant fundus autofluorescence (FAF) features cross-sectionally and longitudinally in a large cohort of patients with inherited retinal diseases (IRDs). Design: Retrospective study of imaging data. Participants: Patients...
6.
Vanzara A, Schiff E, Lin S, Pulido J, Michaelides M, Webster A, et al.
Eye (Lond)
. 2025 Jan;
PMID: 39875726
No abstract available.
7.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A, et al.
medRxiv
. 2025 Jan;
PMID: 39830270
The U4 small nuclear RNA (snRNA) forms a duplex with the U6 snRNA and, together with U5 and ~30 proteins, is part of the U4/U6.U5 tri-snRNP complex, located at the...
8.
Lee C, Wafa H, Murphy G, Galloway J, Mahroo O, Jackson T
BMJ Open Ophthalmol
. 2024 Dec;
9(1.
PMID: 39719323
Introduction: Annual screening for hydroxychloroquine (HCQ) retinopathy is recommended, and electroretinography (ERG) is considered a gold-standard test, but there are screening shortfalls and standard ERG is burdensome and has limited...
9.
Lin S, Arno G, Robson A, Schiff E, Mohamed M, Michaelides M, et al.
Eye (Lond)
. 2024 Dec;
PMID: 39632990
Background: Variants in CRX are associated with dominantly inherited retinopathy with considerable phenotypic variability. Many patients have central retinal degeneration; in some patients, we have observed an additional focus of...
10.
Xu Z, Tan J, Vetrivel K, Jiang X, Leo S, Bhatti T, et al.
Invest Ophthalmol Vis Sci
. 2024 Nov;
65(13):21.
PMID: 39530998
Purpose: One of the strongest genetic associations with myopia is near the GJD2 gene. Recently, this locus was associated with cone-driven electroretinograms (ERGs), with findings highlighting OFF pathway signals specifically....