King‐Wai Yau

28.2k total citations · 10 hit papers
149 papers, 21.2k citations indexed

About

King‐Wai Yau is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, King‐Wai Yau has authored 149 papers receiving a total of 21.2k indexed citations (citations by other indexed papers that have themselves been cited), including 121 papers in Cellular and Molecular Neuroscience, 97 papers in Molecular Biology and 35 papers in Endocrine and Autonomic Systems. Recurrent topics in King‐Wai Yau's work include Photoreceptor and optogenetics research (82 papers), Retinal Development and Disorders (82 papers) and Neurobiology and Insect Physiology Research (37 papers). King‐Wai Yau is often cited by papers focused on Photoreceptor and optogenetics research (82 papers), Retinal Development and Disorders (82 papers) and Neurobiology and Insect Physiology Research (37 papers). King‐Wai Yau collaborates with scholars based in United States, Japan and United Kingdom. King‐Wai Yau's co-authors include Samer Hattar, D. A. Baylor, David M. Berson, Motoharu Takao, Trevor D. Lamb, H.–W. Liao, Kazuhiko Nakatani, Randall R. Reed, Hsi‐Wen Liao and Michael Tri H. and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

King‐Wai Yau

148 papers receiving 20.6k citations

Hit Papers

Melanopsin-Containing Ret... 1979 2026 1994 2010 2002 2005 2003 2006 1979 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
King‐Wai Yau United States 70 13.4k 12.6k 7.0k 3.7k 2.7k 149 21.2k
Martin Biel Germany 64 7.3k 0.5× 11.8k 0.9× 1.2k 0.2× 2.4k 0.6× 890 0.3× 253 17.2k
William Cowan United States 89 16.5k 1.2× 8.3k 0.7× 3.4k 0.5× 1.4k 0.4× 10.8k 4.1× 235 28.9k
Harvey J. Karten United States 71 6.9k 0.5× 5.5k 0.4× 1.2k 0.2× 792 0.2× 3.4k 1.3× 184 14.8k
Shigetada Nakanishi Japan 116 30.6k 2.3× 29.5k 2.4× 2.3k 0.3× 2.4k 0.6× 4.7k 1.8× 344 47.2k
Robert Y. Moore United States 77 11.9k 0.9× 3.6k 0.3× 13.8k 2.0× 1.3k 0.3× 10.0k 3.8× 183 25.5k
Samer Hattar United States 45 5.9k 0.4× 4.7k 0.4× 8.7k 1.2× 1.1k 0.3× 2.6k 1.0× 108 12.2k
Noboru Mizuno Japan 77 18.6k 1.4× 9.7k 0.8× 3.4k 0.5× 2.0k 0.5× 6.0k 2.3× 413 25.9k
Joseph Altman United States 77 11.4k 0.9× 8.3k 0.7× 1.9k 0.3× 1.6k 0.4× 3.1k 1.2× 158 25.1k
D. A. Baylor United States 61 11.2k 0.8× 10.8k 0.9× 720 0.1× 841 0.2× 4.1k 1.6× 98 15.5k
David A. McCormick United States 97 23.4k 1.7× 8.1k 0.6× 2.1k 0.3× 2.2k 0.6× 24.6k 9.3× 200 36.8k

Countries citing papers authored by King‐Wai Yau

Since Specialization
Citations

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

Fields of papers citing papers by King‐Wai Yau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by King‐Wai Yau. 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 King‐Wai Yau. The network helps show where King‐Wai Yau may publish in the future.

Co-authorship network of co-authors of King‐Wai Yau

This figure shows the co-authorship network connecting the top 25 collaborators of King‐Wai Yau. A scholar is included among the top collaborators of King‐Wai Yau 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 King‐Wai Yau. King‐Wai Yau 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.
Chai, Zuying, et al.. (2024). Dark continuous noise from visual pigment as a major mechanism underlying rod–cone difference in light sensitivity. Proceedings of the National Academy of Sciences. 121(51). e2418031121–e2418031121. 1 indexed citations
2.
Tsuji, Tadataka, Vladimir Tolstikov, Yang Zhang, et al.. (2024). Light-responsive adipose-hypothalamus axis controls metabolic regulation. Nature Communications. 15(1). 6768–6768. 4 indexed citations
3.
Chai, Zuying, et al.. (2024). Dark continuous noise from mutant G90D-rhodopsin predominantly underlies congenital stationary night blindness. Proceedings of the National Academy of Sciences. 121(21). e2404763121–e2404763121. 2 indexed citations
4.
Li, Guang, et al.. (2023). Coexistence within one cell of microvillous and ciliary phototransductions across M1- through M6-IpRGCs. Proceedings of the National Academy of Sciences. 120(52). e2315282120–e2315282120. 6 indexed citations
5.
Kim, Yeon Jin, Beth B. Peterson, Joanna D. Crook, et al.. (2022). Origins of direction selectivity in the primate retina. Nature Communications. 13(1). 2862–2862. 30 indexed citations
6.
Jiang, Zheng, et al.. (2017). Novel Phototransduction Pathway in Intrinsically Photosensitive Retinal Ganglion Cells (ipRGCs). Investigative Ophthalmology & Visual Science. 58(8). 4127–4127. 1 indexed citations
7.
Sun, Lu, Zheng Jiang, Michal Rivlin‐Etzion, et al.. (2013). On and Off Retinal Circuit Assembly by Divergent Molecular Mechanisms. Science. 342(6158). 1241974–1241974. 106 indexed citations
8.
Matsuoka, Ryota, Zheng Jiang, Ivy S. Samuels, et al.. (2012). Guidance-Cue Control of Horizontal Cell Morphology, Lamination, and Synapse Formation in the Mammalian Outer Retina. Journal of Neuroscience. 32(20). 6859–6868. 51 indexed citations
9.
Fan, Jie, Keisuke Sakurai, Ching-Kang Chen, et al.. (2010). Deletion of GRK1 Causes Retina Degeneration through a Transducin-Independent Mechanism. Journal of Neuroscience. 30(7). 2496–2503. 15 indexed citations
10.
Shi, Guang, King‐Wai Yau, Jeannie Chen, & Vladimir J. Kefalov. (2007). Signaling Properties of a Short-Wave Cone Visual Pigment and Its Role in Phototransduction. Journal of Neuroscience. 27(38). 10084–10093. 65 indexed citations
11.
Dacey, Dennis M., Hsi‐Wen Liao, Beth B. Peterson, et al.. (2005). Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN. Nature. 433(7027). 749–754. 991 indexed citations breakdown →
12.
Kefalov, Vladimir J., Yingbin Fu, & King‐Wai Yau. (2005). Higher Rate of Thermal Activation of Red Cone Pigments With 11–Cis A2 Compared to 11–Cis A1 Retinal as Chromophore. Investigative Ophthalmology & Visual Science. 46(13). 2264–2264. 3 indexed citations
13.
Kefalov, Vladimir J., Maureen E. Estevez, Masahiro Kono, et al.. (2005). Breaking the Covalent Bond— A Pigment Property that Contributes to Desensitization in Cones. Neuron. 46(6). 879–890. 89 indexed citations
14.
Hattar, Samer, et al.. (2004). Diverse Brain Targets of Melanopsin–Expressing Retinal Ganglion Cells. Investigative Ophthalmology & Visual Science. 45(13). 660–660. 1 indexed citations
15.
Lucas, Robert J., Samer Hattar, Motoharu Takao, et al.. (2003). Diminished Pupillary Light Reflex at High Irradiances in Melanopsin-Knockout Mice. Science. 299(5604). 245–247. 643 indexed citations breakdown →
16.
Hattar, Samer, Robert J. Lucas, Motoharu Takao, et al.. (2003). Diminished Pupillary Light Reflex at High Irradiances in Melanopsin-Knockout Mice. Investigative Ophthalmology & Visual Science. 44(13). 3232–3232. 3 indexed citations
17.
Kefalov, Vladimir J., Yingbin Fu, Nicholas Marsh‐Armstrong, & King‐Wai Yau. (2003). Role of visual pigment properties in rod and cone phototransduction. Nature. 425(6957). 526–531. 107 indexed citations
18.
Sun, Hui, Takashi Tsunenari, King‐Wai Yau, & Jeremy Nathans. (2002). The vitelliform macular dystrophy protein defines a new family of chloride channels. Proceedings of the National Academy of Sciences. 99(6). 4008–4013. 375 indexed citations
19.
Koutalos, Yiannis & King‐Wai Yau. (2000). [49] Characterization of guanylyl cyclase and phosphodiesterase activities in single rod outer segments. Methods in enzymology on CD-ROM/Methods in enzymology. 315. 742–752. 1 indexed citations
20.
Peng, Yuandong, Craig Blackstone, Richard L. Huganir, & King‐Wai Yau. (1995). Distribution of glutamate receptor subtypes in the vertebrate retina. Neuroscience. 66(2). 483–497. 175 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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