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Mark E. Pennesi

oregon health and science university

46H指数
378论文数
7.8K被引数
收录论文 82
发表时间
Assessment of In-Frame Indel Variants in an Unsolved Cohort of Inherited Retinal Diseases Using Machine Learning使用机器学习评估一个未解决的自体遗传性视网膜疾病队列中的同框插入缺失变异。
err2026-03-02
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errOAAI
errDavid E. Rauch; Meng Wang; Muhammad Jafar Hussain Hafiz; Daniel C. Brock; Yumei Li; Molly Marra; Mark E. Pennesi; Paul Yang; Everett Lesley; Irma Lopez; Robert Koenekoop; Edward Ryan Collantes; Joanne Bolinao; Rui Chen
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Corrigendum to “Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.” Am J Ophthalmol. 2020; 219:87-100勘误:“RUSH2A研究中的基线视场发现:相关因素与疾病严重程度其他指标的关联。” 美国眼科杂志。2020; 219:87-100
err2025-08-05
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PREAI
errJacque L. Duncan; Wendi Liang; Maureen G. Maguire; Isabelle Audo; Allison R. Ayala; David G. Birch; Joseph Carroll; Janet K. Cheetham; Simona Degli Esposti; Todd A. Durham; Laura Erker; Sina Farsiu; Frederick L. Ferris; Elise Heon; Robert B. Hufnagel; Alessandro Iannaccone; Glenn J. Jaffe; Christine N. Kay; Michel Michaelides; Mark E. Pennesi; José-Alain Sahel
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Longitudinal Imaging of the Parafoveal Cone Mosaic in Congenital Achromatopsia黄斑旁视锥细胞镶嵌的纵向成像研究先天性全色盲
err2025-07-01
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errOAAI
errChen, Nickolas; Litts, Katie M.; Nikezic, Danica; Langlo, Christopher S.; Higgins, Brian P.; Lam, Byron L.; Fishman, Gerald A.; Collison, Frederick T.; Pennesi, Mark E.; Kay, Christine N.; Tarima, Sergey; Carroll, Joseph
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Characterization of Visual Field Loss Over 4 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) StudyUSH2A相关视网膜变性的视野损失进展率特征:4年随访研究(RUSH2A研究)
err2025-05-22
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PREAI
errDuncan, JL; Maguire, MG; McDaniel, LS; Doucet, NR; Audo, I; Ayala, AR; Cheetham, JK; Cheng, PY; Durham, TA; Huckfeldt, RM; Hufnagel, RB; Jayasundera, KT; Khan, N; Malbin, B; Maldonado, RS; Michaelides, M; Pennesi, ME; Weng, CY; Zmejkoski, A; Aravind, S; Ishikawa, H; Birch, DG
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BASELINE VISUAL FIELD FINDINGS IN THE RUSH2A STUDY: ASSOCIATED FACTORS AND CORRELATION WITH OTHER MEASURES OF DISEASE SEVERITY (vol 219, pg 87, 2020)RUSH2A研究中的基线视场发现:相关因素及与其他疾病严重程度指标的相关性(卷219,页87,2020)
err2025-05-01
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PREAI
errDuncan, JL; Liang, WD; Maguire, MG; Audo, I; Ayala, AR; Birch, DG; Carroll, J; Cheetham, JK; Degli Esposti, S; Durham, TA; Erker, L; Farsiu, S; Ferris, FL III; Heon, E; Hufnagel, RB; Iannacconé, A; Jaffe, GJ; Kay, CN; Michaelides, M; Pennesi, ME; Sahel, JA
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Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapy基因治疗相关葡萄膜炎(GTAU):理解并减轻视网膜基因治疗中的不良免疫反应
err2025-05-01
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errOAAI
errPurdy, Ryan; John, Molly; Bray, Alissa; Clare, Alison J.; Copland, David A.; Chan, Ying Kai; Henderson, Robert H.; Nerinckx, Fanny; Leroy, Bart P.; Yang, Paul; Pennesi, Mark E.; Maclaren, Robert E.; Fischer, M. Dominik; Dick, Andrew D.
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Electroretinography of disease activity and treatment response in birdshot chorioretinopathy鸟枪脉络膜视网膜病变活动性与治疗反应的电生理检查
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IF3.2
err2025-03-28
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PREAI
errRosenberg, Christopher R.; White, Elizabeth; Alsamarraie, Aseel; Suresh, Sandip; Tschetter, Wayne; Choi, Dongseok; Choi, Rene Y.; Weleber, Richard G.; Rosenbaum, James T.; Lin, Phoebe; Pennesi, Mark E.; Suhler, Eric B.; Yang, Paul
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Subretinal Gene Therapy Drug AGTC-501 for XLRP Phase 1/2 Multicenter Study (HORIZON): 24-Month Safety and Efficacy Results
err2025-03-01
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PREAI
errYang, Paul; Birch, David; Lauer, Andreas; Sisk, Robert; Anand, Rajiv; Pennesi, Mark E.; Iannaccone, Alessandro; Yaghy, Antonio; Scaria, Abraham; Jung, Jung Ah; Curtiss, Darin; Waheed, Nadia K.
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Visual Acuity, Full-field Stimulus Thresholds, and Electroretinography for 4 Years in The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) Study
err2025-03-01
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errOAAI
errBirch, David G.; Cheng, Peiyao; Maguire, Maureen G.; Duncan, Jacque L.; Ayala, Allison R.; Cheetham, Janet K.; Doucet, Nicole R.; Durham, Todd A.; Fahim, Abigail T.; Ferris, Frederick L.; Huckfeldt, Rachel M.; Melia, Michele; Michaelides, Michel; Pennesi, Mark E.; Sahel, Jose-Alain; Stingl, Katarina; Vincent, Ajoy; Weng, Christina Y.
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Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll
err2025-02-06
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errBranham, Kari; Samarakoon, Lassana; Audo, Isabelle; Ayala, Allison R.; Cheetham, Janet K.; Daiger, Stephen P.; Dhooge, Patty; Duncan, Jacque L.; Durham, Todd A.; Fahim, Abigail T.; Huckfeldt, Rachel M.; Hufnagel, Robert B.; Kohl, Susanne; Maldonado, Ramiro S.; Melia, Michele; Michaelides, Michel; Pennesi, Mark E.; Sahel, Jose-Alain; Sallum, Juliana M. Ferraz; Singh, Mandeep S.; Sharon, Dror; Stepien, Kimberly; Jones, Kaylie; Weng, Christina Y.
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XOLARIS: A 24-Month, Prospective, Natural History Study of 201 Participants with Retinitis Pigmentosa GTPase Regulator-Associated X-Linked Retinitis Pigmentosa
err2025-01-01
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PREAI
errMacLaren, Robert E.; Duncan, Jacque L.; Fischer, M. Dominik; Lam, Byron L.; Meunier, Isabelle; Pennesi, Mark E.; Sankila, Eeva-Marja K.; Gow, James A.; Li, Jiang; Tsang, So-Fai
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Refractive Error in Inherited Retinal Disease
err2025-01-01
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PREAI
errYassin, Shaden H.; Wagner, Naomi E.; Khuu, Thomas; Schmidt, Ryan; Igelman, Austin D.; Marra, Molly; Schwartz, Hilary; Walker, Evan; Nagiel, Aaron; Yang, Paul; Everett, Lesley A.; Pennesi, Mark E.; Borooah, Shyamanga
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iPSC-Derived LCHADD Retinal Pigment Epithelial Cells Are Susceptible to Lipid Peroxidation and Rescued by Transfection of a Wildtype AAV-HADHA Vector
err2024-09-16
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errOAAI
errDevine, Tiffany; Elizondo, Gabriela; Gaston, Garen; Babcock, Shannon J.; Matern, Dietrich; Shchepinov, Mikhail S.; Pennesi, Mark E.; Harding, Cary O.; Gillingham, Melanie B.
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Assessment of Visual Function with Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study
err2024-09-01
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PREAI
errLam, Byron L.; Pennesi, Mark E.; Kay, Christine N.; Panda, Sushil; Gow, James A.; Zhao, Guolin; MacLaren, Robert E.
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Twelve-month Natural History Study of Centrosomal Protein 290 (CEP290)-associated Inherited Retinal Degeneration
err2024-09-01
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errPierce, Eric A.; Ashimatey, Bright S.; Jayasundera, Thiran; Hoyng, Carel; Lam, Byron L.; Lorenz, Birgit; Kim, Keunpyo; Rashid, Alia; Myers, Rene; Pennesi, Mark E.
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Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study
err2024-07-30
err2
PREAI
errIgelman, Austin D.; White, Elizabeth; Tayyib, Alaa; Everett, Lesley; Vincent, Ajoy; Heon, Elise; Zeitz, Christina; Michaelides, Michel; Mahroo, Omar A.; Katta, Mohamed; Webster, Andrew; Preising, Markus; Lorenz, Birgit; Khateb, Samer; Banin, Eyal; Sharon, Dror; Luski, Shahar; Van Den Broeck, Filip; Leroy, Bart Peter; De Baere, Elfride; Walraedt, Sophie; Stingl, Katarina; Kuehlewein, Laura; Kohl, Susanne; Reith, Milda; Fulton, Anne; Raghuram, Aparna; Meunier, Isabelle; Dollfus, Helene; Aleman, Tomas S.; Bedoukian, Emma C.; O'Neil, Erin C.; Krauss, Emily; Vincent, Andrea; Jordan, Charlotte; Iannaccone, Alessandro; Sen, Parveen; Sundaramurthy, Srilekha; Nagasamy, Soumittra; Balikova, Irina; Casteels, Ingele; Borooah, Shyamanga; Yassin, Shaden; Nagiel, Aaron; Schwartz, Hillary; Zanlonghi, Xavier; Gottlob, Irene; Mclean, Rebecca J.; Munier, Francis L.; Stephenson, Andrew; Sisk, Robert; Koenekoop, Robert; Wilson, Lorri B.; Fredrick, Douglas; Choi, Dongseok; Yang, Paul; Pennesi, Mark Edward
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A Prospective, Observational, Non-interventional Clinical Study of Participants With Choroideremia: The NIGHT Study
err2024-07-01
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PREAI
errMaclaren, Robert E.; Lam, Byron l.; Fischer, M. Dominik; Holz, Frank G.; Pennesi, Mark E.; Birch, David G.; Sankila, Eeva-Marja; Meunier, Isabelle Anne; Stepien, Kimberly E.; Sallum, Juliana Maria Ferraz; Li, Jiang; Yoon, Dan; Panda, Sushil; Gow, James A.
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