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Mark Pennesi

Affiliations: 
University of California, San Francisco, San Francisco, CA 
Area:
Ophthalmology
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"Mark Pennesi"
Cross-listing: Neurotree

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Parents

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Samuel M. Wu grad student Baylor College of Medicine

Children

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Collaborators

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Seung-Yun Yoo collaborator 2001-2003 Baylor College of Medicine
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Publications

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Wongchaisuwat N, Amato A, Yang P, et al. (2024) Optical Coherence Tomography Split-Spectrum Amplitude-Decorrelation Optoretinography Detects Early Central Cone Photoreceptor Dysfunction in Retinal Dystrophies. Translational Vision Science & Technology. 13: 5
DeVine T, Elizondo G, Gaston G, et al. (2024) iPSC-Derived LCHADD Retinal Pigment Epithelial Cells Are Susceptible to Lipid Peroxidation and Rescued by Transfection of a Wildtype AAV-HADHA Vector. Investigative Ophthalmology & Visual Science. 65: 22
Pennesi ME, Wang YZ, Birch DG. (2024) Deep learning aided measurement of outer retinal layer metrics as biomarkers for inherited retinal degenerations: opportunities and challenges. Current Opinion in Ophthalmology. 35: 447-454
Kalaw FGP, Wagner NE, de Oliveira TB, et al. (2024) Using multi-modal imaging to refine the phenotype of PRPH2-associated retinal degeneration. Ophthalmology. Retina
Igelman AD, White E, Tayyib A, et al. (2024) Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study. The British Journal of Ophthalmology
MacLaren RE, Audo I, Fischer MD, et al. (2024) An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study. Human Gene Therapy
Pierce EA, Ashimatey BS, Jayasundera T, et al. (2024) Twelve-month Natural History Study of Centrosomal Protein 290 (CEP290)-associated Inherited Retinal Degeneration. Ophthalmology Science. 4: 100483
Pierce EA, Aleman TS, Jayasundera KT, et al. (2024) Gene Editing for -Associated Retinal Degeneration. The New England Journal of Medicine
Lam BL, Pennesi ME, Kay CN, et al. (2024) Assessment of Visual Function With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study. Ophthalmology
Han JH, Rodenburg K, Hayman T, et al. (2024) Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101106
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