Iain F. Davidson

4.7k total citations · 3 hit papers
30 papers, 2.8k citations indexed

About

Iain F. Davidson is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Iain F. Davidson has authored 30 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 7 papers in Plant Science and 6 papers in Cell Biology. Recurrent topics in Iain F. Davidson's work include Genomics and Chromatin Dynamics (21 papers), RNA and protein synthesis mechanisms (8 papers) and DNA Repair Mechanisms (7 papers). Iain F. Davidson is often cited by papers focused on Genomics and Chromatin Dynamics (21 papers), RNA and protein synthesis mechanisms (8 papers) and DNA Repair Mechanisms (7 papers). Iain F. Davidson collaborates with scholars based in Austria, Germany and United States. Iain F. Davidson's co-authors include Jan‐Michael Peters, Wen Tang, Gordana Wutz, Benedikt Bauer, René Ladurner, Venugopal Bhaskara, Pim J. Huis in ’t Veld, Anatoliy Li, J. Julian Blow and Gabriele Litos and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Iain F. Davidson

29 papers receiving 2.7k citations

Hit Papers

DNA loop extrusion by human cohesin 2019 2026 2021 2023 2019 2021 2023 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iain F. Davidson Austria 21 2.6k 626 407 320 125 30 2.8k
Camilla Sjögren Sweden 24 2.1k 0.8× 406 0.6× 582 1.4× 239 0.7× 139 1.1× 34 2.4k
Elçin Ünal United States 20 2.6k 1.0× 611 1.0× 651 1.6× 254 0.8× 105 0.8× 45 2.8k
Alexander Strunnikov United States 27 3.2k 1.3× 885 1.4× 1.1k 2.6× 411 1.3× 158 1.3× 46 3.5k
Luís Aragón United Kingdom 29 2.9k 1.1× 676 1.1× 658 1.6× 338 1.1× 175 1.4× 54 3.1k
Gordana Wutz Austria 20 2.4k 0.9× 709 1.1× 268 0.7× 253 0.8× 121 1.0× 25 2.7k
Yota Murakami Japan 27 2.2k 0.9× 541 0.9× 535 1.3× 364 1.1× 452 3.6× 78 2.7k
Hisao Masukata Japan 27 2.5k 1.0× 733 1.2× 423 1.0× 722 2.3× 99 0.8× 45 2.7k
Michiko Hirano United States 12 2.5k 1.0× 717 1.1× 886 2.2× 308 1.0× 106 0.8× 13 2.7k
John T. Lis United States 21 2.0k 0.8× 202 0.3× 144 0.4× 211 0.7× 121 1.0× 38 2.2k
Sarah Elderkin United Kingdom 14 1.5k 0.6× 175 0.3× 239 0.6× 392 1.2× 139 1.1× 15 1.7k

Countries citing papers authored by Iain F. Davidson

Since Specialization
Citations

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

Fields of papers citing papers by Iain F. Davidson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Iain F. Davidson. 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 Iain F. Davidson. The network helps show where Iain F. Davidson may publish in the future.

Co-authorship network of co-authors of Iain F. Davidson

This figure shows the co-authorship network connecting the top 25 collaborators of Iain F. Davidson. A scholar is included among the top collaborators of Iain F. Davidson 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 Iain F. Davidson. Iain F. Davidson 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.
Barth, Roman, Iain F. Davidson, Jaco van der Torre, et al.. (2025). SMC motor proteins extrude DNA asymmetrically and can switch directions. Cell. 188(3). 749–763.e21. 15 indexed citations
2.
Barth, Roman, Richard Janissen, Jaco van der Torre, et al.. (2025). Two CTCF motifs impede cohesin-mediated DNA loop extrusion. Molecular Cell. 85(23). 4304–4317.e9. 1 indexed citations
3.
Janissen, Richard, Roman Barth, Iain F. Davidson, Jan‐Michael Peters, & Cees Dekker. (2024). All eukaryotic SMC proteins induce a twist of −0.6 at each DNA loop extrusion step. Science Advances. 10(50). eadt1832–eadt1832. 9 indexed citations
4.
Barth, Roman, Biswajit Pradhan, Eugene Kim, et al.. (2023). Testing pseudotopological and nontopological models for SMC-driven DNA loop extrusion against roadblock-traversal experiments. Scientific Reports. 13(1). 8100–8100. 10 indexed citations
5.
Nagasaka, Kota, Iain F. Davidson, Roman R. Stocsits, et al.. (2023). Cohesin mediates DNA loop extrusion and sister chromatid cohesion by distinct mechanisms. Molecular Cell. 83(17). 3049–3063.e6. 24 indexed citations
6.
Davidson, Iain F., Roman Barth, Jaco van der Torre, et al.. (2023). CTCF is a DNA-tension-dependent barrier to cohesin-mediated loop extrusion. Nature. 616(7958). 822–827. 94 indexed citations breakdown →
7.
Scherr, Matthias J, Hugo B. Brandão, Johanna Gassler, et al.. (2022). MCM complexes are barriers that restrict cohesin-mediated loop extrusion. Nature. 606(7912). 197–203. 86 indexed citations
8.
Pradhan, Biswajit, Roman Barth, Eugene Kim, et al.. (2022). SMC complexes can traverse physical roadblocks bigger than their ring size. Cell Reports. 41(3). 111491–111491. 87 indexed citations
9.
Bauer, Benedikt, Iain F. Davidson, Gordana Wutz, et al.. (2021). Cohesin mediates DNA loop extrusion by a “swing and clamp” mechanism. Cell. 184(21). 5448–5464.e22. 101 indexed citations
10.
Davidson, Iain F. & Jan‐Michael Peters. (2021). Genome folding through loop extrusion by SMC complexes. Nature Reviews Molecular Cell Biology. 22(7). 445–464. 301 indexed citations breakdown →
11.
Wutz, Gordana, René Ladurner, Brian Glenn St Hilaire, et al.. (2020). ESCO1 and CTCF enable formation of long chromatin loops by protecting cohesinSTAG1 from WAPL. eLife. 9. 111 indexed citations
12.
Davidson, Iain F., et al.. (2019). DNA loop extrusion by human cohesin. Science. 366(6471). 1338–1345. 538 indexed citations breakdown →
13.
Soh, Young‐Min, Iain F. Davidson, Stefano Zamuner, et al.. (2019). Self-organization of parS centromeres by the ParB CTP hydrolase. Science. 366(6469). 1129–1133. 94 indexed citations
14.
Holzmann, Johann, Antonio Z. Politi, Kota Nagasaka, et al.. (2019). Absolute quantification of cohesin, CTCF and their regulators in human cells. eLife. 8. 73 indexed citations
15.
Davidson, Iain F., Maxim I. Molodtsov, Pim J. Huis in ’t Veld, et al.. (2016). Rapid movement and transcriptional re‐localization of human cohesin on DNA. The EMBO Journal. 35(24). 2671–2685. 179 indexed citations
16.
Qiao, Renping, Florian Weissmann, Masaya Yamaguchi, et al.. (2016). Mechanism of APC/C CDC20 activation by mitotic phosphorylation. Proceedings of the National Academy of Sciences. 113(19). E2570–8. 108 indexed citations
17.
Brown, Nicholas G., Edmond R. Watson, Florian Weissmann, et al.. (2014). Mechanism of Polyubiquitination by Human Anaphase-Promoting Complex: RING Repurposing for Ubiquitin Chain Assembly. Molecular Cell. 56(2). 246–260. 92 indexed citations
18.
Asencio, Claudio, Iain F. Davidson, Rachel Santarella‐Mellwig, et al.. (2012). Coordination of Kinase and Phosphatase Activities by Lem4 Enables Nuclear Envelope Reassembly during Mitosis. Cell. 150(1). 122–135. 132 indexed citations
19.
Davidson, Iain F., Anatoliy Li, & J. Julian Blow. (2006). Deregulated Replication Licensing Causes DNA Fragmentation Consistent with Head-to-Tail Fork Collision. Molecular Cell. 24(3). 433–443. 114 indexed citations
20.
Davidson, Iain F.. (1983). Non-linear effects in the support motion of an elastically mounted slider crank mechanism. Journal of Sound and Vibration. 86(1). 71–83. 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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