Max E. Wilkinson

2.6k total citations · 3 hit papers
25 papers, 1.6k citations indexed

About

Max E. Wilkinson is a scholar working on Molecular Biology, Ecology and Plant Science. According to data from OpenAlex, Max E. Wilkinson has authored 25 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 5 papers in Ecology and 3 papers in Plant Science. Recurrent topics in Max E. Wilkinson's work include RNA and protein synthesis mechanisms (21 papers), CRISPR and Genetic Engineering (11 papers) and RNA modifications and cancer (10 papers). Max E. Wilkinson is often cited by papers focused on RNA and protein synthesis mechanisms (21 papers), CRISPR and Genetic Engineering (11 papers) and RNA modifications and cancer (10 papers). Max E. Wilkinson collaborates with scholars based in United States, United Kingdom and New Zealand. Max E. Wilkinson's co-authors include Kiyoshi Nagai, Clément Charenton, Sebastian M. Fica, Andrew J. Newman, Wojciech P. Galej, Chris Oubridge, Rhiannon K. Macrae, Feng Zhang, Jonathan Strecker and Linyi Gao and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Max E. Wilkinson

23 papers receiving 1.6k citations

Hit Papers

RNA Splicing by the Spliceosome 2019 2026 2021 2023 2019 2022 2024 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Max E. Wilkinson United States 16 1.4k 151 111 92 91 25 1.6k
Célia Plisson‐Chastang France 18 1.1k 0.8× 269 1.8× 143 1.3× 95 1.0× 87 1.0× 25 1.5k
Philip Mitchell United Kingdom 24 2.7k 1.9× 153 1.0× 100 0.9× 140 1.5× 206 2.3× 33 2.9k
Rhiannon K. Macrae United States 18 1.3k 0.9× 179 1.2× 165 1.5× 56 0.6× 299 3.3× 33 1.6k
Jasminka Boskovic Spain 17 610 0.4× 116 0.8× 59 0.5× 72 0.8× 118 1.3× 35 933
Michaela Rode Germany 13 1.5k 1.1× 122 0.8× 113 1.0× 53 0.6× 149 1.6× 15 1.7k
Andrey V. Pisarev United States 18 2.0k 1.4× 123 0.8× 87 0.8× 38 0.4× 130 1.4× 22 2.2k
Bryan Gibb United States 12 987 0.7× 70 0.5× 120 1.1× 68 0.7× 180 2.0× 14 1.1k
Karim‐Jean Armache United States 17 2.1k 1.5× 233 1.5× 191 1.7× 53 0.6× 358 3.9× 26 2.3k
Prashant Bhat United States 10 1.3k 0.9× 212 1.4× 41 0.4× 165 1.8× 165 1.8× 13 1.4k
Ivan N. Shatsky Russia 22 1.8k 1.3× 130 0.9× 83 0.7× 76 0.8× 170 1.9× 36 2.1k

Countries citing papers authored by Max E. Wilkinson

Since Specialization
Citations

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

Fields of papers citing papers by Max E. Wilkinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Max E. Wilkinson

This figure shows the co-authorship network connecting the top 25 collaborators of Max E. Wilkinson. A scholar is included among the top collaborators of Max E. Wilkinson 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 Max E. Wilkinson. Max E. Wilkinson 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.
Wilkinson, Max E., Daniel Strebinger, Blake Lash, et al.. (2025). Structure and biochemistry-guided engineering of an all-RNA system for DNA insertion with R2 retrotransposons. Nature Communications. 16(1). 6079–6079.
2.
Faure, Guilhem, Makoto Saito, Max E. Wilkinson, et al.. (2025). TIGR-Tas: A family of modular RNA-guided DNA-targeting systems in prokaryotes and their viruses. Science. 388(6746). eadv9789–eadv9789. 17 indexed citations
3.
Zilberzwige‐Tal, Shai, Han Altae-Tran, Soumya Kannan, et al.. (2025). Reprogrammable RNA-targeting CRISPR systems evolved from RNA toxin-antitoxins. Cell. 188(7). 1925–1940.e20. 9 indexed citations
4.
Wilkinson, Max E., et al.. (2024). Control of 3′ splice site selection by the yeast splicing factor Fyv6. eLife. 13. 2 indexed citations
5.
Wilkinson, Max E., et al.. (2024). Control of 3′ splice site selection by the yeast splicing factor Fyv6. eLife. 13. 1 indexed citations
6.
Frangieh, Chris J., Max E. Wilkinson, Daniel Strebinger, et al.. (2024). Internal initiation of reverse transcription in a Penelope-like retrotransposon. Mobile DNA. 15(1). 12–12.
7.
Xu, Peiyu, Makoto Saito, Guilhem Faure, et al.. (2024). Structural insights into the diversity and DNA cleavage mechanism of Fanzor. Cell. 187(19). 5238–5252.e20. 5 indexed citations
8.
Birkholz, Nils, Max E. Wilkinson, Christian Cuba Samaniego, et al.. (2024). Phage anti-CRISPR control by an RNA- and DNA-binding helix–turn–helix protein. Nature. 631(8021). 670–677. 12 indexed citations
9.
Wilkinson, Max E., David Li, Linyi Gao, Rhiannon K. Macrae, & Feng Zhang. (2024). Phage-triggered reverse transcription assembles a toxic repetitive gene from a noncoding RNA. Science. 386(6717). eadq3977–eadq3977. 21 indexed citations
10.
Madigan, Victoria J., Yugang Zhang, Max E. Wilkinson, et al.. (2024). Human paraneoplastic antigen Ma2 (PNMA2) forms icosahedral capsids that can be engineered for mRNA delivery. Proceedings of the National Academy of Sciences. 121(11). e2307812120–e2307812120. 15 indexed citations
11.
Strecker, Jonathan, F. Esra Demircioglu, David Li, et al.. (2022). RNA-activated protein cleavage with a CRISPR-associated endopeptidase. Science. 378(6622). 874–881. 48 indexed citations
12.
Hirano, Seiichi, Kalli Kappel, Han Altae-Tran, et al.. (2022). Structure of the OMEGA nickase IsrB in complex with ωRNA and target DNA. Nature. 610(7932). 575–581. 27 indexed citations
13.
Gao, Linyi, Max E. Wilkinson, Jonathan Strecker, et al.. (2022). Prokaryotic innate immunity through pattern recognition of conserved viral proteins. Science. 377(6607). eabm4096–eabm4096. 138 indexed citations breakdown →
14.
Wilkinson, Max E., Sebastian M. Fica, Wojciech P. Galej, & Kiyoshi Nagai. (2021). Structural basis for conformational equilibrium of the catalytic spliceosome. Molecular Cell. 81(7). 1439–1452.e9. 37 indexed citations
15.
Fica, Sebastian M., Chris Oubridge, Max E. Wilkinson, Andrew J. Newman, & Kiyoshi Nagai. (2019). A human postcatalytic spliceosome structure reveals essential roles of metazoan factors for exon ligation. Science. 363(6428). 710–714. 88 indexed citations
16.
Wilkinson, Max E., Clément Charenton, & Kiyoshi Nagai. (2019). RNA Splicing by the Spliceosome. Annual Review of Biochemistry. 89(1). 359–388. 426 indexed citations breakdown →
17.
Fica, Sebastian M., Chris Oubridge, Wojciech P. Galej, et al.. (2017). Structure of a spliceosome remodelled for exon ligation. Nature. 542(7641). 377–380. 140 indexed citations
18.
Wilkinson, Max E., Sebastian M. Fica, Wojciech P. Galej, et al.. (2017). Postcatalytic spliceosome structure reveals mechanism of 3′–splice site selection. Science. 358(6368). 1283–1288. 89 indexed citations
19.
Galej, Wojciech P., Max E. Wilkinson, Sebastian M. Fica, et al.. (2016). Cryo-EM structure of the spliceosome immediately after branching. Nature. 537(7619). 197–201. 180 indexed citations
20.
Wilkinson, Max E., Yoshio Nakatani, Raymond H.J. Staals, et al.. (2016). Structural plasticity and in vivo activity of Cas1 from the type I-F CRISPR–Cas system. Biochemical Journal. 473(8). 1063–1072. 9 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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