Thomas Surrey

9.9k total citations · 1 hit paper
93 papers, 7.2k citations indexed

About

Thomas Surrey is a scholar working on Cell Biology, Molecular Biology and Condensed Matter Physics. According to data from OpenAlex, Thomas Surrey has authored 93 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Cell Biology, 66 papers in Molecular Biology and 12 papers in Condensed Matter Physics. Recurrent topics in Thomas Surrey's work include Microtubule and mitosis dynamics (80 papers), Photosynthetic Processes and Mechanisms (33 papers) and Cellular Mechanics and Interactions (19 papers). Thomas Surrey is often cited by papers focused on Microtubule and mitosis dynamics (80 papers), Photosynthetic Processes and Mechanisms (33 papers) and Cellular Mechanics and Interactions (19 papers). Thomas Surrey collaborates with scholars based in Germany, United Kingdom and Spain. Thomas Surrey's co-authors include Peter Bieling, Stanislas Leibler, Ivo A. Telley, François Nédélec, Johanna Roostalu, A. C. Maggs, Fritz Jähnig, Eric Karsenti, Nicholas I. Cade and Sebastian P. Maurer and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Thomas Surrey

92 papers receiving 7.1k citations

Hit Papers

Self-organization of microtubules and motors 1997 2026 2006 2016 1997 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Surrey Germany 48 5.0k 4.5k 1.1k 575 554 93 7.2k
Stefan Diez Germany 43 3.7k 0.7× 3.0k 0.7× 1.0k 1.0× 376 0.7× 917 1.7× 175 6.6k
Marileen Dogterom Netherlands 33 4.2k 0.8× 3.4k 0.8× 399 0.4× 675 1.2× 496 0.9× 83 5.6k
William O. Hancock United States 35 3.2k 0.6× 2.3k 0.5× 660 0.6× 348 0.6× 390 0.7× 114 4.2k
Aurélien Roux Switzerland 47 4.8k 1.0× 6.7k 1.5× 265 0.3× 246 0.4× 961 1.7× 120 9.8k
Daniel Needleman United States 34 1.6k 0.3× 1.8k 0.4× 769 0.7× 235 0.4× 418 0.8× 90 3.6k
Patricia Bassereau France 55 3.5k 0.7× 6.8k 1.5× 490 0.5× 135 0.2× 1.6k 2.8× 157 9.6k
Matthieu Piel France 60 6.8k 1.4× 5.0k 1.1× 471 0.4× 429 0.7× 3.1k 5.5× 153 11.5k
Taro Q.P. Uyeda Japan 37 2.7k 0.5× 2.5k 0.5× 502 0.5× 273 0.5× 817 1.5× 134 5.1k
Ron Vale United States 27 4.2k 0.8× 4.1k 0.9× 381 0.4× 408 0.7× 399 0.7× 43 6.6k
G. V. Shivashankar Singapore 40 2.4k 0.5× 3.2k 0.7× 262 0.2× 425 0.7× 1.0k 1.8× 151 5.7k

Countries citing papers authored by Thomas Surrey

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Surrey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Surrey

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Surrey. A scholar is included among the top collaborators of Thomas Surrey 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 Surrey. Thomas Surrey 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.
Nédélec, François, et al.. (2025). Molecular design principles for bipolar spindle organization by two opposing motors. Proceedings of the National Academy of Sciences. 122(12). e2422190122–e2422190122.
2.
Brito, Cláudia, et al.. (2024). Transition of human γ-tubulin ring complex into a closed conformation during microtubule nucleation. Science. 383(6685). 870–876. 23 indexed citations
3.
Brito, Cláudia, et al.. (2023). The minus-end depolymerase KIF2A drives flux-like treadmilling of γTuRC-uncapped microtubules. The Journal of Cell Biology. 222(10). 8 indexed citations
4.
Nédélec, François, et al.. (2023). Effects of microtubule length and crowding on active microtubule network organization. iScience. 26(2). 106063–106063. 5 indexed citations
5.
LaFrance, Benjamin, Johanna Roostalu, Basil J. Greber, et al.. (2022). Structural transitions in the GTP cap visualized by cryo-electron microscopy of catalytically inactive microtubules. Proceedings of the National Academy of Sciences. 119(2). 47 indexed citations
6.
Fineberg, Adam, Thomas Surrey, & Philipp Kukura. (2020). Quantifying the Monomer–Dimer Equilibrium of Tubulin with Mass Photometry. Journal of Molecular Biology. 432(23). 6168–6172. 14 indexed citations
7.
Lera-Ramírez, Manuel, et al.. (2019). Self-Organization of Minimal Anaphase Spindle Midzone Bundles. Current Biology. 29(13). 2120–2130.e7. 34 indexed citations
8.
Jha, Rupam, Johanna Roostalu, Nicholas I. Cade, Martina Trokter, & Thomas Surrey. (2017). Combinatorial regulation of the balance between dynein microtubule end accumulation and initiation of directed motility. The EMBO Journal. 36(22). 3387–3404. 44 indexed citations
9.
Ti, Shih-Chieh, Melissa C. Pamula, Stuart C. Howes, et al.. (2016). Mutations in Human Tubulin Proximal to the Kinesin-Binding Site Alter Dynamic Instability at Microtubule Plus- and Minus-Ends. Developmental Cell. 37(1). 72–84. 81 indexed citations
10.
Roostalu, Johanna, Nicholas I. Cade, & Thomas Surrey. (2015). Complementary activities of TPX2 and chTOG constitute an efficient importin-regulated microtubule nucleation module. Nature Cell Biology. 17(11). 1422–1434. 117 indexed citations
11.
Duellberg, Christian, et al.. (2014). Reconstitution of a hierarchical +TIP interaction network controlling microtubule end tracking of dynein. Nature Cell Biology. 16(8). 804–811. 76 indexed citations
12.
Trokter, Martina, Norbert Mücke, & Thomas Surrey. (2012). Reconstitution of the human cytoplasmic dynein complex. Proceedings of the National Academy of Sciences. 109(51). 20895–20900. 86 indexed citations
13.
Roostalu, Johanna, et al.. (2011). Directional Switching of the Kinesin Cin8 Through Motor Coupling. Science. 332(6025). 94–99. 133 indexed citations
14.
Maurer, Sebastian P., Peter Bieling, Julia Cope, Andreas Hoenger, & Thomas Surrey. (2011). GTPγS microtubules mimic the growing microtubule end structure recognized by end-binding proteins (EBs). Proceedings of the National Academy of Sciences. 108(10). 3988–3993. 165 indexed citations
15.
Bieling, Peter, Ivo A. Telley, Christian Hentrich, Jacob Piehler, & Thomas Surrey. (2010). Fluorescence Microscopy Assays on Chemically Functionalized Surfaces for Quantitative Imaging of Microtubule, Motor, and +TIP Dynamics. Methods in cell biology. 95. 555–580. 85 indexed citations
16.
Espeut, Julien, Amaury Gaussen, Peter Bieling, et al.. (2008). Phosphorylation Relieves Autoinhibition of the Kinetochore Motor Cenp-E. Molecular Cell. 29(5). 637–643. 86 indexed citations
17.
Sung, Hsin-Ho, et al.. (2008). Drosophila Ensconsin Promotes Productive Recruitment of Kinesin-1 to Microtubules. Developmental Cell. 15(6). 866–876. 74 indexed citations
18.
Sarli, Vasiliki, Michael Gärtner, Jeanette Seiler, et al.. (2005). Synthesis and biological evaluation of new tetrahydro-β-carbolines as inhibitors of the mitotic kinesin Eg5. Bioorganic & Medicinal Chemistry. 13(22). 6094–6111. 78 indexed citations
19.
Bringmann, Henrik, et al.. (2004). A Kinesin-like Motor Inhibits Microtubule Dynamic Instability. Science. 303(5663). 1519–1522. 122 indexed citations
20.
Surrey, Thomas, et al.. (2001). Assaying Spatial Organization of Microtubules by Kinesin Motors. Humana Press eBooks. 164. 213–222. 3 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026