Thomas E. Hughes

4.9k total citations · 2 hit papers
64 papers, 3.1k citations indexed

About

Thomas E. Hughes is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biophysics. According to data from OpenAlex, Thomas E. Hughes has authored 64 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 37 papers in Cellular and Molecular Neuroscience and 29 papers in Biophysics. Recurrent topics in Thomas E. Hughes's work include Advanced Fluorescence Microscopy Techniques (29 papers), Photoreceptor and optogenetics research (21 papers) and Retinal Development and Disorders (15 papers). Thomas E. Hughes is often cited by papers focused on Advanced Fluorescence Microscopy Techniques (29 papers), Photoreceptor and optogenetics research (21 papers) and Retinal Development and Disorders (15 papers). Thomas E. Hughes collaborates with scholars based in United States, Estonia and Canada. Thomas E. Hughes's co-authors include Mikhail Drobizhev, Aleksander Rebane, Nikolay S. Makarov, Shane Tillo, Charles O. Boyd, Marc Pypaert, Peter Novick, Lorise C. Gahring, Barbara J. Crain and Scott W. Rogers and has published in prestigious journals such as Science, New England Journal of Medicine and The Journal of Cell Biology.

In The Last Decade

Thomas E. Hughes

64 papers receiving 3.1k citations

Hit Papers

Two-photon absorption pro... 1994 2026 2004 2015 2011 1994 100 200 300 400 500

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Thomas E. Hughes 1.7k 1.3k 859 464 284 64 3.1k
Karl A. Kasischke 878 0.5× 822 0.6× 634 0.7× 399 0.9× 88 0.3× 33 2.6k
Sabine Lévi 2.3k 1.4× 2.0k 1.6× 272 0.3× 278 0.6× 662 2.3× 68 4.2k
Tomomi Nemoto 1.5k 0.9× 1.6k 1.2× 782 0.9× 513 1.1× 245 0.9× 107 4.0k
Harshad D. Vishwasrao 1.2k 0.7× 635 0.5× 603 0.7× 525 1.1× 382 1.3× 30 2.6k
Mazahir T. Hasan 1.9k 1.1× 1.2k 1.0× 551 0.6× 370 0.8× 131 0.5× 44 3.9k
Martin Heine 2.6k 1.6× 2.8k 2.2× 343 0.4× 196 0.4× 241 0.8× 83 4.9k
Gabriele S. Kaminski Schierle 2.5k 1.5× 1.2k 1.0× 755 0.9× 580 1.3× 734 2.6× 121 5.5k
Steven S. Vogel 3.3k 2.0× 1.4k 1.1× 821 1.0× 341 0.7× 265 0.9× 68 5.1k
Varda Lev‐Ram 2.5k 1.5× 2.2k 1.7× 888 1.0× 444 1.0× 191 0.7× 47 5.1k
Oliver Griesbeck 3.5k 2.1× 2.9k 2.2× 1.7k 1.9× 309 0.7× 141 0.5× 64 6.5k

Countries citing papers authored by Thomas E. Hughes

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Hughes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Hughes. 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 Thomas E. Hughes. The network helps show where Thomas E. Hughes may publish in the future.

Co-authorship network of co-authors of Thomas E. Hughes

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Hughes. A scholar is included among the top collaborators of Thomas E. Hughes 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 Thomas E. Hughes. Thomas E. Hughes 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.
Zhang, Jinfan, Bian Liu, Ingie Hong, et al.. (2020). An ultrasensitive biosensor for high-resolution kinase activity imaging in awake mice. Nature Chemical Biology. 17(1). 39–46. 71 indexed citations
2.
Molina, Rosana S., Jonathan King, Nathan Clack, et al.. (2020). High throughput instrument to screen fluorescent proteins under two-photon excitation. Biomedical Optics Express. 11(12). 7192–7192. 5 indexed citations
3.
Qian, Yong, Kiryl D. Piatkevich, Benedict Mc Larney, et al.. (2019). A genetically encoded near-infrared fluorescent calcium ion indicator. Nature Methods. 16(2). 171–174. 162 indexed citations
4.
Harlen, Kevin, et al.. (2019). Live-Cell Assays for Cell Stress Responses Reveal New Patterns of Cell Signaling Caused by Mutations in Rhodopsin, α-Synuclein and TDP-43. Frontiers in Cellular Neuroscience. 13. 535–535. 7 indexed citations
5.
Tewson, Paul, Scott Martinka, Nathan C. Shaner, et al.. (2018). Assay for Detecting Gαi-Mediated Decreases in cAMP in Living Cells. SLAS DISCOVERY. 23(9). 898–906. 11 indexed citations
6.
Piatkevich, Kiryl D., Ho-Jun Suk, Suhasa B. Kodandaramaiah, et al.. (2017). Near-Infrared Fluorescent Proteins Engineered from Bacterial Phytochromes in Neuroimaging. Biophysical Journal. 113(10). 2299–2309. 42 indexed citations
7.
Ding, Yidan, Jiao Li, Jhon R. Enterina, et al.. (2015). Ratiometric biosensors based on dimerization-dependent fluorescent protein exchange. Nature Methods. 12(3). 195–198. 121 indexed citations
8.
Guan, Yinghua, Matthias Meurer, Aleksander Rebane, et al.. (2015). Live-cell multiphoton fluorescence correlation spectroscopy with an improved large Stokes shift fluorescent protein. Molecular Biology of the Cell. 26(11). 2054–2066. 17 indexed citations
9.
Sung, Uhna, et al.. (2015). Improving Signal Dynamics of Fluorescent Protein Voltage Sensors by Optimizing FRET Interactions. Biophysical Journal. 108(2). 152a–152a. 3 indexed citations
10.
Sarkisyan, Karen S., Peter V. Lidsky, D.A. Gorbachev, et al.. (2015). Green Fluorescent Protein with Anionic Tryptophan-Based Chromophore and Long Fluorescence Lifetime. Biophysical Journal. 109(2). 380–389. 53 indexed citations
11.
Stoltzfus, Caleb, et al.. (2014). The Two-Photon Bazooka: A New Way of Optically Screening Randomly Mutagenized Libraries of Fluorescent Proteins. Biophysical Journal. 106(2). 810a–811a. 1 indexed citations
12.
Drobizhev, Mikhail, Thomas E. Hughes, Yuriy Stepanenko, et al.. (2012). Primary Role of the Chromophore Bond Length Alternation in Reversible Photoconversion of Red Fluorescence Proteins. Scientific Reports. 2(1). 688–688. 27 indexed citations
13.
Drobizhev, Mikhail, Shane Tillo, Nikolay S. Makarov, Aleksander Rebane, & Thomas E. Hughes. (2010). Color Hues in Fluorescent Proteins with the Same Chromophore are due to Internal Quadratic Stark Effect. Biophysical Journal. 98(3). 413a–413a. 1 indexed citations
14.
Drobizhev, Mikhail, Shane Tillo, Nikolay S. Makarov, Aleksander Rebane, & Thomas E. Hughes. (2009). Absolute Two-photon Absorption Spectra Of Orange And Red Fluorescent Proteins. Biophysical Journal. 96(3). 400a–401a. 1 indexed citations
15.
Miranda, Pablo, et al.. (2008). FRET with multiply labeled HERG K+ channels as a reporter of the in vivo coarse architecture of the cytoplasmic domains. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783(10). 1681–1699. 22 indexed citations
17.
Giráldez, Teresa, Thomas E. Hughes, & Fred J. Sigworth. (2005). Generation of Functional Fluorescent BK Channels by Random Insertion of GFP Variants. The Journal of General Physiology. 126(5). 429–438. 43 indexed citations
18.
Rex, Tonia S., Enrico Maria Surace, Alberto Auricchio, et al.. (2004). EGFP levels and toxicity in transgenic and virus injected animals.. Investigative Ophthalmology & Visual Science. 45(13). 3707–3707. 1 indexed citations
19.
Molloy, Raymond, et al.. (1998). Ionotropic glutamate receptors in the retina: Moving from molecules to circuits. Vision Research. 38(10). 1399–1410. 21 indexed citations
20.
Hughes, Thomas E.. (1994). Transmembrane topology of the glutamate receptors. Journal of Molecular Neuroscience. 5(4). 211–217. 6 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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