Paul A. Sieving, MD PhD

Affiliations: 
1985-2001 Ophthalmology University of Michigan Medical School Ann Arbor 
 2001-2016 National Eye Institute, Bethesda, Maryland 
Area:
visual system, retina, genetics, retinal degeneration, gene therapy, Biomedical Engineering, Ophthalmology, Neuroscience Biology
Google:
"Paul Sieving"
Mean distance: 18.28
 

Collaborators

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J Bernard Heymann collaborator (Computational Biology Tree)
Laura Frishman collaborator 1982- University of Houston College of Optometry
Ronald A. Bush collaborator 1990- NEI
BETA: Related publications

Publications

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Zeng Y, Qian H, Wu Z, et al. (2019) AAVrh-10 transduces outer retinal cells in rodents and rabbits following intravitreal administration. Gene Therapy
Turriff A, Blain D, Similuk M, et al. (2019) Motivations and Decision-Making Processes of Men with X-linked Retinoschisis Considering Participation in an Ocular Gene Therapy Trial. American Journal of Ophthalmology
Song H, Bush RA, Zeng Y, et al. (2019) Trans-ocular Electric Current Enhances AAV-Mediated Retinal Gene Transduction after Intravitreal Vector Administration. Molecular Therapy. Methods & Clinical Development. 13: 77-85
Mott MC, Austin CP, Bianchi DW, et al. (2019) The NIH Blueprint for Neuroscience Research Seeks Community Input on Future Neuroscience Investments. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 39: 774-775
Heymann JB, Vijayasarathy C, Huang RK, et al. (2019) Cryo-EM of retinoschisin branched networks suggests an intercellular adhesive scaffold in the retina. The Journal of Cell Biology
Bianchi DW, Cooper JA, Gordon JA, et al. (2018) Neuroethics for the National Institutes of Health BRAIN Initiative. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 38: 10583-10585
Cukras C, Wiley HE, Jeffrey BG, et al. (2018) Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery. Molecular Therapy : the Journal of the American Society of Gene Therapy. 26: 2282-2294
Li L, Jiao X, D'Atri I, et al. (2018) Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. Plos Genetics. 14: e1007504
Cukras CA, Huryn LA, Jeffrey BP, et al. (2018) Analysis of Anatomic and Functional Measures in X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 59: 2841-2847
Chekuri A, Guru AA, Biswas P, et al. (2018) IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. Human Genetics
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