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Mark Pennesi
Mark Pennesi
Professor of Ophthalmology, Oregon Health & Science University
Verified email at ohsu.edu
Title
Cited by
Cited by
Year
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
7002015
Animal models of age related macular degeneration
ME Pennesi, M Neuringer, RJ Courtney
Molecular aspects of medicine 33 (4), 487-509, 2012
4272012
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
3111999
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
2482003
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
2252016
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
1632019
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
1512012
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
1362003
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
1242010
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
1242007
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
1222004
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
1182003
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
1142004
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
1142002
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
1132020
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
1132016
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
1042015
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
1022016
Effects of elevated intraocular pressure on mouse retinal ganglion cells
J Ji, P Chang, ME Pennesi, Z Yang, J Zhang, D Li, SM Wu, RL Gross
Vision research 45 (2), 169-179, 2005
1002005
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
992019
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