Rachel Wong

15.4k total citations · 4 hit papers
151 papers, 11.6k citations indexed

About

Rachel Wong is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Rachel Wong has authored 151 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 121 papers in Cellular and Molecular Neuroscience, 116 papers in Molecular Biology and 20 papers in Cognitive Neuroscience. Recurrent topics in Rachel Wong's work include Retinal Development and Disorders (108 papers), Neuroscience and Neuropharmacology Research (86 papers) and Photoreceptor and optogenetics research (85 papers). Rachel Wong is often cited by papers focused on Retinal Development and Disorders (108 papers), Neuroscience and Neuropharmacology Research (86 papers) and Photoreceptor and optogenetics research (85 papers). Rachel Wong collaborates with scholars based in United States, Australia and United Kingdom. Rachel Wong's co-authors include Carla J. Shatz, Markus Meister, Wai T. Wong, Anirvan Ghosh, D. A. Baylor, Haruhisa Okawa, Luca Della Santina, Mrinalini Hoon, Jaime Grutzendler and Fred Rieke and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Rachel Wong

148 papers receiving 11.4k citations

Hit Papers

Synchronous Bursts of Action Potentials in Ganglion Cells... 1991 2026 2002 2014 1991 2001 2002 2014 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rachel Wong United States 55 7.8k 7.5k 2.0k 1.6k 1.3k 151 11.6k
Richard H. Masland United States 55 9.6k 1.2× 7.8k 1.0× 2.1k 1.0× 799 0.5× 386 0.3× 110 12.2k
Dennis D.M. O’Leary United States 76 7.7k 1.0× 10.4k 1.4× 2.4k 1.2× 2.8k 1.7× 5.1k 4.0× 127 16.1k
Herwig Baier United States 64 6.2k 0.8× 5.1k 0.7× 2.2k 1.1× 5.9k 3.6× 960 0.7× 129 11.8k
Anton Reiner United States 68 4.6k 0.6× 7.1k 0.9× 1.9k 0.9× 796 0.5× 812 0.6× 218 12.6k
Heinz Wässle Germany 83 16.2k 2.1× 14.4k 1.9× 3.8k 1.9× 1.3k 0.8× 337 0.3× 157 19.3k
Andrew D. Huberman United States 41 4.2k 0.5× 4.3k 0.6× 1.8k 0.9× 489 0.3× 939 0.7× 66 8.6k
R. W. Guillery United States 64 5.6k 0.7× 7.6k 1.0× 6.6k 3.2× 1.4k 0.9× 1.2k 0.9× 149 13.9k
Christine E. Holt United Kingdom 67 10.0k 1.3× 8.2k 1.1× 786 0.4× 4.5k 2.8× 2.5k 1.9× 146 15.3k
Raymond D. Lund United States 63 8.0k 1.0× 8.3k 1.1× 2.7k 1.3× 714 0.4× 2.6k 2.0× 225 13.9k
Carlos Portera‐Cailliau United States 39 3.3k 0.4× 3.6k 0.5× 1.7k 0.9× 554 0.3× 1.1k 0.9× 71 7.5k

Countries citing papers authored by Rachel Wong

Since Specialization
Citations

This map shows the geographic impact of Rachel Wong'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 Rachel Wong with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Wong more than expected).

Fields of papers citing papers by Rachel Wong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rachel Wong. 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 Rachel Wong. The network helps show where Rachel Wong may publish in the future.

Co-authorship network of co-authors of Rachel Wong

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Wong. A scholar is included among the top collaborators of Rachel Wong 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 Rachel Wong. Rachel Wong 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.
Wong, Rachel, et al.. (2025). Tidal Synchronization of TESS Eclipsing Binaries. The Astrophysical Journal. 990(2). 124–124. 1 indexed citations
2.
Sheng, Alexander Y., et al.. (2025). Five-Year Trends in Emergency Medicine Match Results and Future Outlook. Western Journal of Emergency Medicine. 26(5). 1392–1396.
3.
Yu, Wan‐Qing, et al.. (2024). A presynaptic source drives differing levels of surround suppression in two mouse retinal ganglion cell types. Nature Communications. 15(1). 599–599. 6 indexed citations
4.
Levin, Leonard A., Michael F. Chiang, Michael A. Dyer, et al.. (2023). Translational roadmap for regenerative therapies of eye disease. Med. 4(9). 583–590. 1 indexed citations
5.
Gelder, Russell N. Van, Michael F. Chiang, Michael A. Dyer, et al.. (2022). Regenerative and restorative medicine for eye disease. Nature Medicine. 28(6). 1149–1156. 68 indexed citations
6.
Grimes, William N., Mrinalini Hoon, Takeshi Yoshimatsu, et al.. (2021). A High-Density Narrow-Field Inhibitory Retinal Interneuron with Direct Coupling to Müller Glia. Journal of Neuroscience. 41(28). 6018–6037. 12 indexed citations
7.
Okawa, Haruhisa, Wan‐Qing Yu, Ulf Matti, et al.. (2019). Dynamic assembly of ribbon synapses and circuit maintenance in a vertebrate sensory system. Nature Communications. 10(1). 2167–2167. 28 indexed citations
8.
Packer, Orin, Richard Schalek, Rachel Wong, et al.. (2017). Restricted cone connections of horizontal cells in the human foveal center. Investigative Ophthalmology & Visual Science. 58(8). 1035–1035. 2 indexed citations
9.
Jorstad, Nikolas L., Matthew S. Wilken, William N. Grimes, et al.. (2017). Stimulation of functional neuronal regeneration from Müller glia in adult mice. Nature. 548(7665). 103–107. 339 indexed citations
10.
Hoshino, Akina, Rinki Ratnapriya, Matthew J. Brooks, et al.. (2017). Molecular Anatomy of the Developing Human Retina. Developmental Cell. 43(6). 763–779.e4. 169 indexed citations
11.
Sinha, Raunak, Mrinalini Hoon, Jacob Baudin, et al.. (2017). Cellular and Circuit Mechanisms Shaping the Perceptual Properties of the Primate Fovea. Cell. 168(3). 413–426.e12. 116 indexed citations
12.
Sharpe, James & Rachel Wong. (2011). Imaging in developmental biology : a laboratory manual. 31 indexed citations
13.
Parker, Steve, et al.. (2010). How many constraints are there? A preliminary inventory of OT phonological constraints. 1 indexed citations
14.
Huckfeldt, Rachel M., Timm Schubert, Josh Morgan, et al.. (2008). Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions. Nature Neuroscience. 12(1). 35–43. 78 indexed citations
15.
Godinho, Leanne, Philip R. Williams, Y. Claassen, et al.. (2007). Nonapical Symmetric Divisions Underlie Horizontal Cell Layer Formation in the Developing Retina In Vivo. Neuron. 56(4). 597–603. 99 indexed citations
16.
Mumm, Jeff S., Leanne Godinho, Josh Morgan, et al.. (2004). Laminar circuit formation in the vertebrate retina. Progress in brain research. 147. 155–169. 40 indexed citations
17.
Gan, Wen-Biao, Jaime Grutzendler, Wai T. Wong, Rachel Wong, & Jeff W. Lichtman. (2000). Multicolor “DiOlistic” Labeling of the Nervous System Using Lipophilic Dye Combinations. Neuron. 27(2). 219–225. 277 indexed citations
18.
Shields, Colleen R., Peter D. Lukasiewicz, & Rachel Wong. (1996). Gabaergic modulation of spontaneous bursting activity in the developing ferret retina. Investigative Ophthalmology & Visual Science. 37(3). 2 indexed citations
19.
Lukasiewicz, Peter D. & Rachel Wong. (1996). The properties of GABAC receptors on ferret retinal bipolar cells. Investigative Ophthalmology & Visual Science. 37(3). 2 indexed citations
20.
Wong, Rachel, Markus Meister, & Carla J. Shatz. (1993). Transient period of correlated bursting activity during development of the mammalian retina. Neuron. 11(5). 923–938. 416 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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