Alexander Sher

13.2k total citations · 3 hit papers
90 papers, 9.0k citations indexed

About

Alexander Sher is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Alexander Sher has authored 90 papers receiving a total of 9.0k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Cellular and Molecular Neuroscience, 50 papers in Cognitive Neuroscience and 40 papers in Molecular Biology. Recurrent topics in Alexander Sher's work include Neuroscience and Neural Engineering (54 papers), Photoreceptor and optogenetics research (41 papers) and Retinal Development and Disorders (40 papers). Alexander Sher is often cited by papers focused on Neuroscience and Neural Engineering (54 papers), Photoreceptor and optogenetics research (41 papers) and Retinal Development and Disorders (40 papers). Alexander Sher collaborates with scholars based in United States, Poland and United Kingdom. Alexander Sher's co-authors include A. M. Litke, E. J. Chichilnisky, Jonathon Shlens, Ben A. Barres, Stephen J Smith, Benjamin K. Stafford, W. Dąbrowski, Paweł Hottowy, Greg D. Field and Liam Paninski and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Alexander Sher

87 papers receiving 8.8k citations

Hit Papers

The Classical Complement Cascade Mediates CNS Synapse Eli... 2007 2026 2013 2019 2007 2013 2008 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Alexander Sher United States 37 4.7k 3.3k 2.6k 2.2k 1.5k 90 9.0k
Hongkui Zeng United States 58 6.9k 1.5× 4.5k 1.4× 6.6k 2.6× 1.6k 0.7× 312 0.2× 128 16.6k
Wen‐Biao Gan United States 44 6.4k 1.4× 3.3k 1.0× 3.1k 1.2× 5.2k 2.3× 289 0.2× 90 13.9k
Yi Zuo United States 35 3.6k 0.8× 1.7k 0.5× 1.7k 0.7× 3.0k 1.4× 228 0.2× 77 7.8k
Kouichi Hashimoto Japan 58 6.0k 1.3× 1.5k 0.4× 4.8k 1.8× 1.9k 0.8× 817 0.5× 203 11.0k
Ania K. Majewska United States 33 3.9k 0.8× 1.5k 0.5× 1.8k 0.7× 2.7k 1.2× 185 0.1× 102 7.0k
Axel Nimmerjahn United States 29 4.0k 0.9× 1.6k 0.5× 2.6k 1.0× 5.8k 2.6× 232 0.2× 39 11.3k
Graham Knott Switzerland 53 6.9k 1.5× 3.3k 1.0× 4.1k 1.6× 1.9k 0.9× 476 0.3× 140 13.2k
Kristina D. Micheva United States 30 2.7k 0.6× 969 0.3× 2.4k 0.9× 2.2k 1.0× 141 0.1× 52 6.9k
Alfredo Kirkwood United States 46 6.4k 1.4× 4.3k 1.3× 3.1k 1.2× 1.1k 0.5× 585 0.4× 99 9.8k
Masanobu Kano Japan 84 15.9k 3.4× 6.0k 1.8× 7.8k 3.0× 4.3k 1.9× 435 0.3× 300 23.3k

Countries citing papers authored by Alexander Sher

Since Specialization
Citations

This map shows the geographic impact of Alexander Sher's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alexander Sher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexander Sher more than expected).

Fields of papers citing papers by Alexander Sher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander Sher. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alexander Sher. The network helps show where Alexander Sher may publish in the future.

Co-authorship network of co-authors of Alexander Sher

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Sher. A scholar is included among the top collaborators of Alexander Sher based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alexander Sher. Alexander Sher is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hottowy, Paweł, W. Dąbrowski, Alexander Sher, et al.. (2024). Understanding responses to multi-electrode epiretinal stimulation using a biophysical model. Journal of Neural Engineering. 22(1). 16010–16010. 1 indexed citations
2.
Wu, Eric, Nora Brackbill, Alexandra Kling, et al.. (2024). Fixational eye movements enhance the precision of visual information transmitted by the primate retina. Nature Communications. 15(1). 7964–7964. 5 indexed citations
3.
Shah, Nishal P., Sasidhar Madugula, Lauren E. Grosberg, et al.. (2024). Precise control of neural activity using dynamically optimized electrical stimulation. eLife. 13. 2 indexed citations
4.
Shah, Nishal P., Georges Goetz, Sasidhar Madugula, et al.. (2023). Inferring light responses of primate retinal ganglion cells using intrinsic electrical signatures. Journal of Neural Engineering. 20(4). 45001–45001. 5 indexed citations
5.
Shah, Nishal P., Nora Brackbill, Alexandra Kling, et al.. (2020). Inference of nonlinear receptive field subunits with spike-triggered clustering. eLife. 9. 20 indexed citations
6.
Shah, Nishal P., Sasidhar Madugula, Paweł Hottowy, et al.. (2019). Efficient characterization of electrically evoked responses for neural interfaces. Neural Information Processing Systems. 32. 14421–14431. 2 indexed citations
7.
Merel, Josh, Nora Brackbill, Alexander Sher, et al.. (2017). Multilayer Recurrent Network Models of Primate Retinal Ganglion Cell Responses. International Conference on Learning Representations. 26 indexed citations
8.
Shah, Nishal P., Nora Brackbill, Georges Goetz, et al.. (2016). Novel Model-based identification of retinal ganglion cell subunits. Investigative Ophthalmology & Visual Science. 57(12). 1 indexed citations
9.
Greschner, Martin, Greg D. Field, Peter H. Li, et al.. (2016). Identification of a Retinal Circuit for Recurrent Suppression Using Indirect Electrical Imaging. Current Biology. 26(15). 1935–1942. 12 indexed citations
10.
Grosberg, Lauren E., Paweł Hottowy, Lauren H. Jepson, et al.. (2015). Axon activation with focal epiretinal stimulation in primate retina. Investigative Ophthalmology & Visual Science. 56(7). 780–780. 1 indexed citations
11.
Palanker, Daniel, Henri Lorach, Georges Goetz, et al.. (2014). Photovoltaic Restoration of Sight in Rats with Retinal Degeneration: Assessment of Spatial Resolution and Visual Functions. Investigative Ophthalmology & Visual Science. 55(13). 5964–5964. 2 indexed citations
12.
Greschner, Martin, Greg D. Field, Peter H. Li, et al.. (2014). A Polyaxonal Amacrine Cell Population in the Primate Retina. Journal of Neuroscience. 34(10). 3597–3606. 45 indexed citations
13.
Beier, Corinne, Jennifer Kung, Philip Huie, et al.. (2014). Bipolar Cells Restructure Dendrites After Selective Ablation of Photoreceptors. Investigative Ophthalmology & Visual Science. 55(13). 4171–4171. 1 indexed citations
14.
Triplett, Jason W., Cory Pfeiffenberger, Jena Yamada, et al.. (2011). Competition is a driving force in topographic mapping. Proceedings of the National Academy of Sciences. 108(47). 19060–19065. 44 indexed citations
15.
Jones, Bryan W., et al.. (2011). Neural Activity in the Inner Retina After Photocoagulation. Investigative Ophthalmology & Visual Science. 52(14). 1170–1170. 4 indexed citations
16.
Sher, Alexander, Loh-Shan Leung, Theodore Leng, et al.. (2010). Retinal Plasticity and Restoration of Function After Photocoagulation. Investigative Ophthalmology & Visual Science. 51(13). 2482–2482. 3 indexed citations
17.
Leung, Loh-Shan, Theodore Leng, Yannis M. Paulus, et al.. (2010). Restorative Retinal Photocoagulation. Investigative Ophthalmology & Visual Science. 51(13). 5579–5579. 1 indexed citations
18.
Field, Greg D., Martin Greschner, Jeffrey L. Gauthier, et al.. (2009). High-sensitivity rod photoreceptor input to the blue-yellow color opponent pathway in macaque retina. Nature Neuroscience. 12(9). 1159–1164. 86 indexed citations
19.
Sher, Alexander, Jeffrey L. Gauthier, Greg D. Field, et al.. (2009). Functional Identification of Individual Cones in the Receptive Fields of Primate Retinal Ganglion Cells. Investigative Ophthalmology & Visual Science. 50(13). 6150–6150. 1 indexed citations
20.
Field, Greg D., Jeffrey L. Gauthier, Martin Greschner, et al.. (2008). Light Adaptation Changes the Size of Receptive Fields in Seven Distinct Primate Retinal Ganglion Cell Types. Investigative Ophthalmology & Visual Science. 49(13). 3856–3856. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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