| Choroideremia: a review of general findings and pathogenesis RG Coussa, EI Traboulsi Ophthalmic genetics 33 (2), 57-65, 2012 | 133 | 2012 |
| Gene therapy for RPE65-related retinal disease V Miraldi Utz, RG Coussa, F Antaki, EI Traboulsi Ophthalmic genetics 39 (6), 671-677, 2018 | 127 | 2018 |
| Cell–matrix interactions in the eye: From cornea to choroid AE Pouw, MA Greiner, RG Coussa, C Jiao, IC Han, JM Skeie, JH Fingert, ... Cells 10 (3), 687, 2021 | 76 | 2021 |
| WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome RG Coussa, EA Otto, HY Gee, P Arthurs, H Ren, I Lopez, V Keser, Q Fu, ... Clinical genetics 84 (2), 150-159, 2013 | 74 | 2013 |
| Surgical management of lens subluxation in Marfan syndrome VM Utz, RG Coussa, EI Traboulsi Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2014 | 63 | 2014 |
| Choroideremia: effect of age on visual acuity in patients and female carriers RG Coussa, J Kim, EI Traboulsi Ophthalmic genetics 33 (2), 66-73, 2012 | 61 | 2012 |
| Stickler syndrome: exploring prophylaxis for retinal detachment RG Coussa, J Sears, EI Traboulsi Current opinion in ophthalmology 30 (5), 306-313, 2019 | 47 | 2019 |
| Accuracy of automated machine learning in classifying retinal pathologies from ultra-widefield pseudocolour fundus images F Antaki, RG Coussa, G Kahwati, K Hammamji, M Sebag, R Duval British Journal of Ophthalmology 107 (1), 90-95, 2023 | 43 | 2023 |
| Genotype and phenotype studies in autosomal dominant retinitis pigmentosa (adRP) of the French Canadian founder population RG Coussa, C Chakarova, R Ajlan, M Taha, C Kavalec, J Gomolin, ... Investigative ophthalmology & visual science 56 (13), 8297-8305, 2015 | 39 | 2015 |
| Sector retinitis pigmentosa: Report of ten cases and a review of the literature RG Coussa, D Basali, A Maeda, M DeBenedictis, EI Traboulsi Molecular vision 25, 869, 2019 | 37 | 2019 |
| Leber congenital amaurosis, from darkness to light: an ode to Irene Maumenee RG Coussa, I Lopez Solache, RK Koenekoop Ophthalmic genetics 38 (1), 7-15, 2017 | 34 | 2017 |
| Predictive modeling of proliferative vitreoretinopathy using automated machine learning by ophthalmologists without coding experience F Antaki, G Kahwati, J Sebag, RG Coussa, A Fanous, R Duval, M Sebag Scientific reports 10 (1), 19528, 2020 | 32 | 2020 |
| Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease VM Utz, RG Coussa, MJ Marino, AV Chappelow, GJ Pauer, SA Hagstrom, ... British Journal of Ophthalmology 98 (4), 513-518, 2014 | 30 | 2014 |
| Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literature RG Coussa, Y Zhao, MJ DeBenedictis, A Babiuch, J Sears, EI Traboulsi Ophthalmic Genetics 41 (1), 63-68, 2020 | 29 | 2020 |
| Treatment of cystic cavities in X-linked juvenile retinoschisis: The first sequential cross-over treatment regimen with dorzolamide RG Coussa, MA Kapusta American Journal of Ophthalmology Case Reports 8, 1-3, 2017 | 19 | 2017 |
| Expression of PRPF31 and TFPT: regulation in health and retinal disease AM Rose, AZ Shah, NH Waseem, CF Chakarova, G Alfano, RG Coussa, ... Human molecular genetics 21 (18), 4126-4137, 2012 | 19 | 2012 |
| Mitochondrial DNA A3243G variant-associated retinopathy: current perspectives and clinical implications RG Coussa, S Parikh, EI Traboulsi Survey of Ophthalmology 66 (5), 838-855, 2021 | 18 | 2021 |
| The prognostic value of peripheral retinal nonperfusion in diabetic retinopathy using ultra-widefield fluorescein angiography F Antaki, RG Coussa, M Mikhail, C Archambault, DE Lederer Graefe's Archive for Clinical and Experimental Ophthalmology 258, 2681-2690, 2020 | 18 | 2020 |
| Post-transplant venous thromboembolic events and their effect on graft survival N Abualhassan, M Aljiffry, L Thalib, R Coussa, P Metrakos, M Hassanain Saudi Journal of Kidney Diseases and Transplantation 26 (1), 1-5, 2015 | 17 | 2015 |
| Propagation and selectivity of axonal loss in Leber hereditary optic neuropathy RG Coussa, P Merat, LA Levin Scientific Reports 9 (1), 6720, 2019 | 15 | 2019 |
Elias TraboulsiCole Eye Institute, Cleveland Clinic在 ccf.org 的电子邮件经过验证
