Bing-Yi Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Bing-Yi Wang has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Andrew Shin
Department of Material Science, Stanford University
1 shared publication- Chuanben Chen
Department of Radiation Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, China
1 shared publication - Daniel Palanker
Stanford University
1 shared publication - Efstathios Vounotrypidis
Department of Ophthalmology, University Hospital Ulm, Ulm, Germany
1 shared publication - Fei Zheng
Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Department of Radiation Oncology, Fujian, China
1 shared publication - Keith Mathieson
University of Strathclyde
1 shared publication
Latest Publications
- Open Access
- 16 February 2023
- Published by Elsevier in Brazilian Journal of Otorhinolaryngology
- Vol. 89 (3) , 374-382
The effect of primary tumor volume on the prognosis of nasopharyngeal carcinoma in era of volumetric modulated arc therapy: a propensity score matched cohort study
- 16 February 2023
- Published by Elsevier in Brazilian Journal of Otorhinolaryngology
- Vol. 89 (3) , 374-382
Open AccessThe effect of primary tumor volume on the prognosis of nasopharyngeal carcinoma in era of volumetric modulated arc therapy: a propensity score matched cohort study
- Open Access
Cellular integration with a subretinal honeycomb-shaped prosthesis
In patients blinded by geographic atrophy, subretinal photovoltaic implant with 100µm pixels provided visual acuity closely matching the pixel pitch. However, such flat bipolar pixels cannot be scaled below 75µm, limiting the attainable visual acuity. This limitation can be overcome by shaping the electric field with 3-dimensional electrodes. In particular, elevating the return electrode on top of honeycomb-shaped vertical walls surrounding each pixel extends the electric field vertically and decouples its penetration into tissue from the pixel width. This approach relies on migration of the retinal cells into the honeycomb wells. Here, we demonstrate that the majority of the inner retinal neurons migrate into 25µm deep wells, leaving the third-order neurons, such as amacrine and ganglion cells, outside. This is important for selective stimulation of the second-order neurons to preserve the retinal signal processing in prosthetic vision. Comparable glial response to that with flat implants suggests that migration and separation of the retinal cells by the walls does not cause additional stress. Furthermore, retinal migration into the honeycombs does not negatively affect its electrical excitability.
Open AccessCellular integration with a subretinal honeycomb-shaped prosthesis
In patients blinded by geographic atrophy, subretinal photovoltaic implant with 100µm pixels provided visual acuity closely matching the pixel pitch. However, such flat bipolar pixels cannot be scaled below 75µm, limiting the attainable visual acuity. This limitation can be overcome by shaping the electric field with 3-dimensional electrodes. In particular, elevating the return electrode on top of honeycomb-shaped vertical walls surrounding each pixel extends the electric field vertically and decouples its penetration into tissue from the pixel width. This approach relies on migration of the retinal cells into the honeycomb wells. Here, we demonstrate that the majority of the inner retinal neurons migrate into 25µm deep wells, leaving the third-order neurons, such as amacrine and ganglion cells, outside. This is important for selective stimulation of the second-order neurons to preserve the retinal signal processing in prosthetic vision. Comparable glial response to that with flat implants suggests that migration and separation of the retinal cells by the walls does not cause additional stress. Furthermore, retinal migration into the honeycombs does not negatively affect its electrical excitability.