Jonathan Cook

958 total citations
23 papers, 725 citations indexed

About

Jonathan Cook is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Jonathan Cook has authored 23 papers receiving a total of 725 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Immunology and 5 papers in Genetics. Recurrent topics in Jonathan Cook's work include Toxin Mechanisms and Immunotoxins (8 papers), Transgenic Plants and Applications (5 papers) and Connexins and lens biology (4 papers). Jonathan Cook is often cited by papers focused on Toxin Mechanisms and Immunotoxins (8 papers), Transgenic Plants and Applications (5 papers) and Connexins and lens biology (4 papers). Jonathan Cook collaborates with scholars based in United Kingdom, Germany and United States. Jonathan Cook's co-authors include Lynne M. Roberts, Janet M. Lord, Daniel C. Smith, Robert A. Spooner, David J. Evans, Nicholas Dale, Philip J. Day, Kym Lowry, Andrew Woodman and Peter Watson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Jonathan Cook

23 papers receiving 720 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan Cook United Kingdom 16 329 319 220 128 103 23 725
Martin B. Dorner Germany 22 571 1.7× 485 1.5× 164 0.7× 42 0.3× 66 0.6× 53 1.6k
Maria Rita Spinosa Italy 13 112 0.3× 430 1.3× 49 0.2× 219 1.7× 89 0.9× 17 903
Chiara Rodighiero United States 7 245 0.7× 468 1.5× 99 0.5× 431 3.4× 77 0.7× 9 880
Annabel Guichard United States 13 139 0.4× 519 1.6× 47 0.2× 145 1.1× 130 1.3× 19 719
Christopher J. Langford Australia 15 142 0.4× 765 2.4× 35 0.2× 60 0.5× 99 1.0× 19 1.2k
Amit P. Mehrotra United Kingdom 7 73 0.2× 464 1.5× 69 0.3× 32 0.3× 140 1.4× 8 720
Amanda Nga-Sze Mak Hong Kong 13 199 0.6× 583 1.8× 159 0.7× 16 0.1× 109 1.1× 16 903
Lucien Cabanié France 11 242 0.7× 332 1.0× 26 0.1× 77 0.6× 122 1.2× 14 738
Jeman Kim Japan 17 202 0.6× 501 1.6× 26 0.1× 51 0.4× 267 2.6× 50 834
Ronald S. Boshuizen Netherlands 19 324 1.0× 464 1.5× 210 1.0× 12 0.1× 193 1.9× 27 1.0k

Countries citing papers authored by Jonathan Cook

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan Cook

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Cook

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Cook. A scholar is included among the top collaborators of Jonathan Cook 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 Jonathan Cook. Jonathan Cook 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
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Cook, Jonathan, et al.. (2023). Activator-induced conformational changes regulate division-associated peptidoglycan amidases. Proceedings of the National Academy of Sciences. 120(24). e2302580120–e2302580120. 15 indexed citations
3.
Bhandare, Amol, et al.. (2020). Connexin26 mediates CO2-dependent regulation of breathing via glial cells of the medulla oblongata. Communications Biology. 3(1). 521–521. 28 indexed citations
4.
Cook, Jonathan, et al.. (2020). Insights into bacterial cell division from a structure of EnvC bound to the FtsX periplasmic domain. Proceedings of the National Academy of Sciences. 117(45). 28355–28365. 36 indexed citations
5.
Nijjar, Sarbjit, et al.. (2019). Structural determinants of CO2-sensitivity in the β connexin family suggested by evolutionary analysis. Communications Biology. 2(1). 331–331. 20 indexed citations
6.
Cook, Jonathan, et al.. (2019). Cx26 keratitis ichthyosis deafness syndrome mutations trigger alternative splicing of Cx26 to prevent expression and cause toxicityin vitro. Royal Society Open Science. 6(8). 191128–191128. 11 indexed citations
7.
Cook, Jonathan, et al.. (2017). Evolutionary adaptation of the sensitivity of connexin26 hemichannels to CO 2. Proceedings of the Royal Society B Biological Sciences. 284(1848). 20162723–20162723. 18 indexed citations
8.
Cook, Jonathan, et al.. (2016). Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro. Physiological Reports. 4(22). e13038–e13038. 13 indexed citations
9.
Tuplin, Andrew, et al.. (2015). Inhibition of HCV translation by disrupting the structure and interactions of the viral CRE and 3′ X-tail. Nucleic Acids Research. 43(5). 2914–2926. 31 indexed citations
10.
Lowry, Kym, Andrew Woodman, Jonathan Cook, & David J. Evans. (2014). Recombination in Enteroviruses Is a Biphasic Replicative Process Involving the Generation of Greater-than Genome Length ‘Imprecise’ Intermediates. PLoS Pathogens. 10(6). e1004191–e1004191. 62 indexed citations
11.
Pietroni, Paola, N. Vasisht, Jonathan Cook, et al.. (2013). The proteasome cap RPT5/Rpt5p subunit prevents aggregation of unfolded ricin A chain. Biochemical Journal. 453(3). 435–445. 14 indexed citations
12.
Redmann, Veronika, et al.. (2011). Dislocation of Ricin Toxin A Chains in Human Cells Utilizes Selective Cellular Factors. Journal of Biological Chemistry. 286(24). 21231–21238. 28 indexed citations
13.
Mayerhofer, Peter, et al.. (2009). Ricin A Chain Insertion into Endoplasmic Reticulum Membranes Is Triggered by a Temperature Increase to 37 °C. Journal of Biological Chemistry. 284(15). 10232–10242. 40 indexed citations
14.
Spooner, Robert A., Jonathan Cook, Paola Pietroni, et al.. (2008). Cytosolic chaperones influence the fate of a toxin dislocated from the endoplasmic reticulum. Proceedings of the National Academy of Sciences. 105(45). 17408–17413. 61 indexed citations
15.
Cook, Jonathan & Malcolm A. McCrae. (2004). Sequence analysis of the guanylyltransferase (VP3) of group A rotaviruses. Journal of General Virology. 85(4). 929–932. 22 indexed citations
16.
Spooner, Robert A., Peter Watson, Catherine J. Marsden, et al.. (2004). Protein disulphide-isomerase reduces ricin to its A and B chains in the endoplasmic reticulum. Biochemical Journal. 383(2). 285–293. 118 indexed citations
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Cook, Jonathan, Philip Savage, Jonathan Lord, & Lynne M. Roberts. (1993). Biologically active interleukin 2-ricin A chain fusion proteins may require intracellular proteolytic cleavage to exhibit A cytotoxic effect. Bioconjugate Chemistry. 4(6). 440–447. 21 indexed citations
20.
Beavil, Andrew J., Rebecca L. Beavil, Christina M.W. Chan, et al.. (1993). Structural basis of the IgE-FcɛRI interaction. Biochemical Society Transactions. 21(4). 968–972. 18 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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