Brett Jeffrey, PhD

Affiliations: 
National Institutes of Health, Bethesda, MD 
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"Brett Jeffrey"
Mean distance: 16.54 (cluster 29)
 
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Publications

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Li J, Liu T, Flynn OJ, et al. (2021) Persistent Dark Cones in Oligocone Trichromacy Revealed by Multimodal Adaptive Optics Ophthalmoscopy. Frontiers in Aging Neuroscience. 13: 629214
Uddin D, Jeffrey BG, Flynn O, et al. (2020) Repeatability of Scotopic Sensitivity and Dark Adaptation Using a Medmont Dark-Adapted Chromatic Perimeter in Age-related Macular Degeneration. Translational Vision Science & Technology. 9: 31
Flynn OJ, Jeffrey BG. (2019) Scotopic contour and shape discrimination using radial frequency patterns. Journal of Vision. 19: 7
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
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
Flynn OJ, Cukras CA, Jeffrey BG. (2018) Characterization of Rod Function Phenotypes Across a Range of Age-Related Macular Degeneration Severities and Subretinal Drusenoid Deposits. Investigative Ophthalmology & Visual Science. 59: 2411-2421
Cukras C, Jeffrey BG. (2017) The Importance of Outcome Measure Research in Stargardt Disease. Jama Ophthalmology
Jeffrey BG, Cukras CA, Vitale S, et al. (2014) Test-Retest Intervisit Variability of Functional and Structural Parameters in X-Linked Retinoschisis. Translational Vision Science & Technology. 3: 5
Zein WM, Jeffrey BG, Wiley HE, et al. (2014) CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone function. Investigative Ophthalmology & Visual Science. 55: 6301-8
Huynh N, Jeffrey BG, Turriff A, et al. (2014) Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindness. Ophthalmic Genetics. 35: 51-6
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