Adam Dubis

Affiliations: 
Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Adaptive Optics, Visual Neuroscience
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"Adam Dubis"
Mean distance: 17.39 (cluster 17)
 
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Publications

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Toledo-Cortés S, Dubis AM, González FA, et al. (2023) Deep Density Estimation for Cone Counting and Diagnosis of Genetic Eye Diseases From Adaptive Optics Scanning Light Ophthalmoscope Images. Translational Vision Science & Technology. 12: 25
Jackson DJ, Dubis AM, Moosajee M. (2022) The Natural History of -Related Retinopathy: A Longitudinal Phenotypic Analysis. International Journal of Molecular Sciences. 23
Gill JS, Theofylaktopoulos V, Mitsios A, et al. (2022) Investigating Biomarkers for Retinopathy Using Multimodal Retinal Imaging. International Journal of Molecular Sciences. 23
Sampson DM, Dubis AM, Chen FK, et al. (2022) Towards standardizing retinal optical coherence tomography angiography: a review. Light, Science & Applications. 11: 63
Jolly JK, Simunovic MP, Dubis AM, et al. (2021) Structural and Functional Characteristics of Color Vision Changes in Choroideremia. Frontiers in Neuroscience. 15: 729807
Hanumunthadu D, Keane PA, Balaskas K, et al. (2021) Agreement Between Spectral-Domain and Swept-Source Optical Coherence Tomography Retinal Thickness Measurements in Macular and Retinal Disease. Ophthalmology and Therapy
Gopalakrishnan S, Mehrvar S, Maleki S, et al. (2020) Photobiomodulation preserves mitochondrial redox state and is retinoprotective in a rodent model of retinitis pigmentosa. Scientific Reports. 10: 20382
Nunez do Rio JM, Sen P, Rasheed R, et al. (2020) Deep Learning-Based Segmentation and Quantification of Retinal Capillary Non-Perfusion on Ultra-Wide-Field Retinal Fluorescein Angiography. Journal of Clinical Medicine. 9
Sarkar H, Dubis AM, Downes S, et al. (2020) Novel Heterozygous Deletion in Retinol Dehydrogenase 12 () Causes Familial Autosomal Dominant Retinitis Pigmentosa. Frontiers in Genetics. 11: 335
Toms M, Dubis AM, de Vrieze E, et al. (2020) Clinical and preclinical therapeutic outcome metrics for USH2A-related disease. Human Molecular Genetics
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