| Germline BAP1 alterations in familial uveal melanoma K Rai, R Pilarski, G Boru, M Rehman, AH Saqr, JB Massengill, A Singh, ... Genes, Chromosomes and Cancer 56 (2), 168-174, 2017 | 76 | 2017 |
| Visual acuity loss and associated risk factors in the retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2) X Kong, RW Strauss, M Michaelides, AV Cideciyan, JA Sahel, B Muñoz, ... Ophthalmology 123 (9), 1887-1897, 2016 | 66 | 2016 |
| A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16) BR Pattnaik, PK Shahi, MJ Marino, X Liu, N York, S Brar, J Chiang, ... Human mutation 36 (7), 720-727, 2015 | 60 | 2015 |
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| Relationship between different fluorescein and indocyanine green angiography features in multiple evanescent white dot syndrome R dell’Omo, R Wong, M Marino, K Konstantopoulou, C Pavesio British journal of ophthalmology 94 (1), 59-63, 2010 | 48 | 2010 |
| Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients CM Cebulla, EM Binkley, R Pilarski, JB Massengill, K Rai, DA Liebner, ... Ophthalmic genetics 36 (2), 126-131, 2015 | 47 | 2015 |
| Genetics of retinoblastoma A Mallipatna, M Marino, AD Singh Asia-Pacific Journal of Ophthalmology 5 (4), 260-264, 2016 | 44 | 2016 |
| Intraoperative OCT imaging of the Argus II retinal prosthesis system AV Rachitskaya, A Yuan, MJ Marino, J Reese, JP Ehlers Ophthalmic Surgery, Lasers and Imaging Retina 47 (11), 999-1003, 2016 | 35 | 2016 |
| Autosomal Dominant Retinitis Pigmentosa Secondary to Pre-mRNA Splicing-Factor Gene PRPF31 (RP11): Review of Disease Mechanism and Report of a Family … VM Utz, CD Beight, MJ Marino, SA Hagstrom, EI Traboulsi Ophthalmic genetics 34 (4), 183-188, 2013 | 32 | 2013 |
| 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 |
| Longitudinal changes of fixation location and stability within 12 months in Stargardt disease: ProgStar Report No. 12 EM Schönbach, RW Strauss, X Kong, B Muñoz, MA Ibrahim, JS Sunness, ... American journal of ophthalmology 193, 54-61, 2018 | 25 | 2018 |
| Faster sensitivity loss around dense scotomas than for overall macular sensitivity in Stargardt disease: ProgStar Report No. 14 EM Schönbach, RW Strauss, MA Ibrahim, JL Janes, DG Birch, ... American journal of ophthalmology 216, 219-225, 2020 | 24 | 2020 |
| Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations VL Bonilha, ME Rayborn, BA Bell, MJ Marino, GA Fishman, JG Hollyfield Ophthalmic genetics 37 (2), 150-160, 2016 | 23 | 2016 |
| Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations VL Bonilha, ME Rayborn, BA Bell, MJ Marino, GJ Pauer, CD Beight, ... Graefe's Archive for Clinical and Experimental Ophthalmology 253, 295-305, 2015 | 23 | 2015 |
| Toxoplasma gondii: an atypical presentation of toxoplasma as optic disc swelling and hemispherical retinal vein occlusion treated with intravitreal clindamycin R Wong, R dell’Omo, M Marino, B Hussein, N Okhravi, CE Pavesio International ophthalmology 29, 195-198, 2009 | 22 | 2009 |
| Congenital uveal melanoma? AD Singh, LA Schoenfield, BC Bastian, HA Aziz, MJ Marino, CV Biscotti Survey of Ophthalmology 61 (1), 59-64, 2016 | 15 | 2016 |
| Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations VL Bonilha, ME Rayborn, BA Bell, MJ Marino, CD Beight, GJ Pauer, ... Graefe's Archive for Clinical and Experimental Ophthalmology 253, 2161-2169, 2015 | 12 | 2015 |
| Germline large deletion of BAP1 and decreased expression in non‐tumor choroid in uveal melanoma patients with high risk for inherited cancer G Boru, TW Grosel, R Pilarski, M Stautberg, JB Massengill, J Jeter, ... Genes, Chromosomes and Cancer 58 (9), 650-656, 2019 | 11 | 2019 |
| Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia SH Lim, ES Germain, KN Tran-Viet, S Staffieri, M Marino, PH Dollfus, ... Ophthalmic genetics 35 (1), 1-6, 2014 | 6 | 2014 |
| Identification of three ABCA4 sequence variations exclusive to African American patients in a cohort of patients with Stargardt disease VM Utz, AV Chappelow, MJ Marino, CD Beight, GM Sturgill-Short, ... American Journal of Ophthalmology 156 (6), 1220-1227. e2, 2013 | 6 | 2013 |
