| Quantitative optical coherence tomography angiography of vascular abnormalities in the living human eye Y Jia, ST Bailey, TS Hwang, SM McClintic, SS Gao, ME Pennesi, ... Proceedings of the National Academy of Sciences 112 (18), E2395-E2402, 2015 | 727 | 2015 |
| Animal models of age related macular degeneration ME Pennesi, M Neuringer, RJ Courtney Molecular aspects of medicine 33 (4), 487-509, 2012 | 441 | 2012 |
| UV-and midwave-sensitive cone-driven retinal responses of the mouse: a possible phenotype for coexpression of cone photopigments AL Lyubarsky, B Falsini, ME Pennesi, P Valentini, EN Pugh Journal of Neuroscience 19 (1), 442-455, 1999 | 316 | 1999 |
| SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity SY Yoo, ME Pennesi, EJ Weeber, B Xu, R Atkinson, S Chen, ... Neuron 37 (3), 383-401, 2003 | 252 | 2003 |
| Results at 2 years after gene therapy for RPE65-deficient Leber congenital amaurosis and severe early-childhood–onset retinal dystrophy RG Weleber, ME Pennesi, DJ Wilson, S Kaushal, LR Erker, L Jensen, ... Ophthalmology 123 (7), 1606-1620, 2016 | 227 | 2016 |
| Lipid nanoparticles for delivery of messenger RNA to the back of the eye S Patel, RC Ryals, KK Weller, ME Pennesi, G Sahay Journal of Controlled Release 303, 91-100, 2019 | 177 | 2019 |
| Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomography ME Pennesi, KV Michaels, SS Magee, A Maricle, SP Davin, AK Garg, ... Investigative ophthalmology & visual science 53 (8), 4644-4656, 2012 | 155 | 2012 |
| BETA2/NeuroD1 null mice: a new model for transcription factor-dependent photoreceptor degeneration ME Pennesi, JH Cho, Z Yang, SH Wu, J Zhang, SM Wu, MJ Tsai Journal of Neuroscience 23 (2), 453-461, 2003 | 136 | 2003 |
| The effects of PEGylation on LNP based mRNA delivery to the eye RC Ryals, S Patel, C Acosta, M McKinney, ME Pennesi, G Sahay PLoS One 15 (10), e0241006, 2020 | 130 | 2020 |
| Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa S Walia, GA Fishman, SG Jacobson, TS Aleman, RK Koenekoop, ... Ophthalmology 117 (6), 1190-1198, 2010 | 129 | 2010 |
| Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet–Biedl syndrome MM Abd-El-Barr, K Sykoudis, S Andrabi, ER Eichers, ME Pennesi, PL Tan, ... Vision research 47 (27), 3394-3407, 2007 | 127 | 2007 |
| Intravitreal voriconazole: an electroretinographic and histopathologic study H Gao, ME Pennesi, K Shah, X Qiao, SM Hariprasad, WF Mieler, SM Wu, ... Archives of ophthalmology 122 (11), 1687-1692, 2004 | 124 | 2004 |
| A mouse model of elevated intraocular pressure: retina and optic nerve findings. RL Gross, J Ji, P Chang, ME Pennesi, Z Yang, J Zhang, SM Wu Transactions of the American Ophthalmological Society 101, 163, 2003 | 119 | 2003 |
| Long-term follow-up of patients with retinitis pigmentosa receiving intraocular ciliary neurotrophic factor implants DG Birch, LD Bennett, JL Duncan, RG Weleber, ME Pennesi American journal of ophthalmology 170, 10-14, 2016 | 115 | 2016 |
| The transcription factor Bhlhb4 is required for rod bipolar cell maturation DE Bramblett, ME Pennesi, SM Wu, MJ Tsai Neuron 43 (6), 779-793, 2004 | 115 | 2004 |
| GCAP1 rescues rod photoreceptor response in GCAP1/GCAP2 knockout mice KA Howes, ME Pennesi, I Sokal, J Church‐Kopish, B Schmidt, D Margolis, ... The EMBO journal, 2002 | 115 | 2002 |
| Residual foveal cone structure in CNGB3-associated achromatopsia CS Langlo, EJ Patterson, BP Higgins, P Summerfelt, MM Razeen, ... Investigative ophthalmology & visual science 57 (10), 3984-3995, 2016 | 112 | 2016 |
| Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium DA Thompson, RR Ali, E Banin, KE Branham, JG Flannery, DM Gamm, ... Investigative ophthalmology & visual science 56 (2), 918-931, 2015 | 106 | 2015 |
| Assessing photoreceptor structure in retinitis pigmentosa and Usher syndrome LW Sun, RD Johnson, CS Langlo, RF Cooper, MM Razeen, MC Russillo, ... Investigative Ophthalmology & Visual Science 57 (6), 2428-2442, 2016 | 105 | 2016 |
| The natural history of inherited retinal dystrophy due to biallelic mutations in the RPE65 gene DC Chung, M Bertelsen, B Lorenz, ME Pennesi, BP Leroy, CP Hamel, ... American journal of ophthalmology 199, 58-70, 2019 | 103 | 2019 |
