Ronald Chalmers

2.6k total citations
56 papers, 2.0k citations indexed

About

Ronald Chalmers is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Ronald Chalmers has authored 56 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 16 papers in Plant Science and 14 papers in Genetics. Recurrent topics in Ronald Chalmers's work include CRISPR and Genetic Engineering (21 papers), Chromosomal and Genetic Variations (16 papers) and Advanced biosensing and bioanalysis techniques (15 papers). Ronald Chalmers is often cited by papers focused on CRISPR and Genetic Engineering (21 papers), Chromosomal and Genetic Variations (16 papers) and Advanced biosensing and bioanalysis techniques (15 papers). Ronald Chalmers collaborates with scholars based in United Kingdom, United States and Canada. Ronald Chalmers's co-authors include Nancy Kleckner, Corentin Claeys Bouuaert, Christoph M. Tang, Karen Lipkow, Nicolas Buisine, Julien Bischerour, Danxu Liu, Sven Sewitz, Paul K. Crellin and Yaohui Sun and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Ronald Chalmers

56 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ronald Chalmers United Kingdom 26 1.4k 551 527 346 309 56 2.0k
Mark S. Thomas United Kingdom 25 939 0.7× 383 0.7× 604 1.1× 348 1.0× 140 0.5× 68 1.8k
Dorit Amikam Israel 17 1.4k 1.0× 584 1.1× 671 1.3× 282 0.8× 254 0.8× 27 2.4k
Alfonso H. Magadán Canada 11 2.3k 1.6× 298 0.5× 545 1.0× 1.0k 2.9× 196 0.6× 13 2.7k
Bradford S. Powell United States 25 1.2k 0.9× 298 0.5× 944 1.8× 626 1.8× 181 0.6× 43 2.1k
Małgorzata Łobocka Poland 22 937 0.7× 343 0.6× 471 0.9× 1.2k 3.3× 404 1.3× 37 1.8k
Jonathan Filée France 21 1.3k 0.9× 779 1.4× 284 0.5× 872 2.5× 87 0.3× 36 2.0k
Dmitri A. Ryjenkov United States 8 1.4k 1.0× 367 0.7× 692 1.3× 180 0.5× 142 0.5× 8 1.9k
Emily J. Stevens United Kingdom 10 1000 0.7× 240 0.4× 391 0.7× 183 0.5× 131 0.4× 17 1.7k
Pier Paolo Di Nocera Italy 23 1.3k 0.9× 524 1.0× 299 0.6× 141 0.4× 78 0.3× 43 1.6k
Elisabeth A. Raleigh United States 28 2.2k 1.6× 428 0.8× 1.1k 2.1× 863 2.5× 83 0.3× 54 2.8k

Countries citing papers authored by Ronald Chalmers

Since Specialization
Citations

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

Fields of papers citing papers by Ronald Chalmers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ronald Chalmers

This figure shows the co-authorship network connecting the top 25 collaborators of Ronald Chalmers. A scholar is included among the top collaborators of Ronald Chalmers 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 Ronald Chalmers. Ronald Chalmers 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.
Chalmers, Ronald, et al.. (2019). Targeted DNA transposition in vitro using a dCas9-transposase fusion protein. Nucleic Acids Research. 47(15). 8126–8135. 25 indexed citations
2.
Tellier, Michael & Ronald Chalmers. (2019). The roles of the human SETMAR (Metnase) protein in illegitimate DNA recombination and non-homologous end joining repair. DNA repair. 80. 26–35. 12 indexed citations
3.
Bouuaert, Corentin Claeys & Ronald Chalmers. (2017). A single active site in the mariner transposase cleaves DNA strands of opposite polarity. Nucleic Acids Research. 45(20). 11467–11478. 7 indexed citations
4.
Gravato‐Nobre, Maria J., Filipa Vaz, Sérgio R. Filipe, Ronald Chalmers, & Jonathan Hodgkin. (2016). The Invertebrate Lysozyme Effector ILYS-3 Is Systemically Activated in Response to Danger Signals and Confers Antimicrobial Protection in C. elegans. PLoS Pathogens. 12(8). e1005826–e1005826. 36 indexed citations
5.
Liu, Danxu & Ronald Chalmers. (2013). Hyperactive mariner transposons are created by mutations that disrupt allosterism and increase the rate of transposon end synapsis. Nucleic Acids Research. 42(4). 2637–2645. 25 indexed citations
6.
Xu, Zhengyao, Louise Thomas, Benjamin Davies, et al.. (2013). Accuracy and efficiency define Bxb1 integrase as the best of fifteen candidate serine recombinases for the integration of DNA into the human genome. BMC Biotechnology. 13(1). 87–87. 74 indexed citations
7.
Bouuaert, Corentin Claeys & Ronald Chalmers. (2013). Hsmar1 Transposition Is Sensitive to the Topology of the Transposon Donor and the Target. PLoS ONE. 8(1). e53690–e53690. 17 indexed citations
8.
Loh, Edmund, Elisabeth Kugelberg, Alexander Tracy, et al.. (2013). Temperature triggers immune evasion by Neisseria meningitidis. Nature. 502(7470). 237–240. 110 indexed citations
9.
Marzo, Mar, Danxu Liu, Alfredo Ruíz, & Ronald Chalmers. (2013). Identification of multiple binding sites for the THAP domain of the Galileo transposase in the long terminal inverted-repeats. Gene. 525(1). 84–91. 8 indexed citations
10.
Haniford, David B., et al.. (2011). H-NS mediates the dissociation of a refractory protein-DNA complex during Tn10/IS10 transposition. Nucleic Acids Research. 39(15). 6660–6668. 9 indexed citations
11.
Siddique, Azeem, Nicolas Buisine, & Ronald Chalmers. (2011). The Transposon-Like Correia Elements Encode Numerous Strong Promoters and Provide a Potential New Mechanism for Phase Variation in the Meningococcus. PLoS Genetics. 7(1). e1001277–e1001277. 29 indexed citations
12.
Chalmers, Ronald, et al.. (2010). Delivering the goods: viral and non-viral gene therapy systems and the inherent limits on cargo DNA and internal sequences. Genetica. 138(5). 485–498. 66 indexed citations
13.
Bischerour, Julien, Ping Lu, David B. Roth, & Ronald Chalmers. (2009). Base Flipping in V(D)J Recombination: Insights into the Mechanism of Hairpin Formation, the 12/23 Rule, and the Coordination of Double-Strand Breaks. Molecular and Cellular Biology. 29(21). 5889–5899. 19 indexed citations
14.
Bischerour, Julien & Ronald Chalmers. (2009). Base Flipping in Tn10 Transposition: An Active Flip and Capture Mechanism. PLoS ONE. 4(7). e6201–e6201. 22 indexed citations
15.
Bouuaert, Corentin Claeys & Ronald Chalmers. (2009). Transposition of the human Hsmar1 transposon: rate-limiting steps and the importance of the flanking TA dinucleotide in second strand cleavage. Nucleic Acids Research. 38(1). 190–202. 36 indexed citations
16.
Bouuaert, Corentin Claeys & Ronald Chalmers. (2009). Gene therapy vectors: the prospects and potentials of the cut-and-paste transposons. Genetica. 138(5). 473–484. 34 indexed citations
17.
Muñoz-López, Martín, Azeem Siddique, Julien Bischerour, et al.. (2008). Transposition of Mboumar-9: Identification of a New Naturally Active mariner-Family Transposon. Journal of Molecular Biology. 382(3). 567–572. 41 indexed citations
18.
Tang, Christoph M., Dave Stroud, Katherine Makepeace, et al.. (2002). Genetic linkage analysis to identify a gene required for the addition of phosphoethanolamine to meningococcal lipopolysaccharide. Gene. 284(1-2). 133–140. 6 indexed citations
19.
Sun, Yaohui, et al.. (2000). Functional genomics of Neisseria meningitidis pathogenesis. Nature Medicine. 6(11). 1269–1273. 165 indexed citations
20.

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

Breakdown of academic impact, for papers by Mark S. Thomas Breakdown of academic impact, for papers by Dorit Amikam Breakdown of academic impact, for papers by Alfonso H. Magadán Breakdown of academic impact, for papers by Bradford S. Powell Breakdown of academic impact, for papers by Małgorzata Łobocka Breakdown of academic impact, for papers by Jonathan Filée Breakdown of academic impact, for papers by Dmitri A. Ryjenkov Breakdown of academic impact, for papers by Emily J. Stevens Breakdown of academic impact, for papers by Pier Paolo Di Nocera Breakdown of academic impact, for papers by Elisabeth A. Raleigh
Rankless by CCL
2026