Razek Georges Coussa

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 6

Top Venues

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

McGill University (BSC)

This page only lists publications with an associated author ORCID identifier.

Education History

McGill University

Canada

BSC :: Chemical Engineering

Publications

Omar Babar Saeed, Elias I Traboulsi, Razek Georges Coussa
Profiling of visual acuity and genotype correlations in RP2 patients: a cross-sectional comparative meta-analysis between carrier females and affected males. Eye (London, England) (2022)
Razek Georges Coussa, Elliott H Sohn, Ian C Han, Sumit Parikh, Elias I Traboulsi
Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations. Ophthalmic genetics 42 (4) (2021)
Razek Georges Coussa, Nikita Lomis, Fares Antaki, Jason Samle, Kavita Patel, George Christodoulou, Satya Prakash, James Oestreicher, Bryan Arthurs
Blink detection and magnetic force generation for correction of lagophthalmos, with specific regard to implant compatibility testing. Orbit (Amsterdam, Netherlands) (2020)
Razek Georges Coussa, Yue Zhao, Meghan J M DeBenedictis, Allison Babiuch, Jonathan Sears, Elias I Traboulsi
Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literature. Ophthalmic genetics 41 (1) (2020)
Fares Antaki, Razek Georges Coussa, Mikel Mikhail, Cyril Archambault, David E Lederer
The prognostic value of peripheral retinal nonperfusion in diabetic retinopathy using ultra-widefield fluorescein angiography. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 258 (12) (2020)
Yue Zhao, Razek Georges Coussa, Meghan J M DeBenedictis, Elias I Traboulsi
Retinal dystrophy associated with a Kizuna (KIZ) mutation and a predominantly macular phenotype. Ophthalmic genetics 40 (5) (2019)

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Publication Activity (10 Years)

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Razek Georges Coussa