Gemma C. Atkinson

4.8k total citations · 1 hit paper
62 papers, 3.1k citations indexed

About

Gemma C. Atkinson is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Gemma C. Atkinson has authored 62 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 19 papers in Genetics and 17 papers in Ecology. Recurrent topics in Gemma C. Atkinson's work include RNA and protein synthesis mechanisms (46 papers), RNA modifications and cancer (21 papers) and Bacterial Genetics and Biotechnology (19 papers). Gemma C. Atkinson is often cited by papers focused on RNA and protein synthesis mechanisms (46 papers), RNA modifications and cancer (21 papers) and Bacterial Genetics and Biotechnology (19 papers). Gemma C. Atkinson collaborates with scholars based in Sweden, Estonia and Germany. Gemma C. Atkinson's co-authors include Vasili Hauryliuk, Tanel Tenson, Katsuhiko Murakami, Kenn Gerdes, Daniel N. Wilson, Chayan Kumar Saha, Victoriia Murina, Sandra L. Baldauf, Hiraku Takada and Alex J. O’Neill and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Gemma C. Atkinson

61 papers receiving 3.1k citations

Hit Papers

Recent functional insights into the role of (p)ppGpp in b... 2015 2026 2018 2022 2015 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
Gemma C. Atkinson Sweden 30 2.3k 1.0k 631 490 312 62 3.1k
Vasili Hauryliuk Sweden 35 3.1k 1.4× 1.7k 1.6× 821 1.3× 658 1.3× 425 1.4× 92 4.3k
Douglas F. Browning United Kingdom 30 2.4k 1.1× 1.7k 1.6× 757 1.2× 309 0.6× 323 1.0× 71 3.6k
Natalie Verstraeten Belgium 24 1.5k 0.7× 966 0.9× 422 0.7× 635 1.3× 267 0.9× 52 2.6k
Pierre Genevaux France 31 2.5k 1.1× 1.1k 1.0× 548 0.9× 304 0.6× 419 1.3× 64 3.2k
Jue D. Wang United States 32 2.8k 1.2× 2.0k 1.9× 771 1.2× 348 0.7× 271 0.9× 58 3.6k
Agata L. Starosta Germany 24 2.4k 1.1× 734 0.7× 405 0.6× 461 0.9× 296 0.9× 40 3.2k
Philippe Bouloc France 31 2.4k 1.1× 1.7k 1.6× 839 1.3× 299 0.6× 430 1.4× 73 3.3k
Irine Ronin Israel 12 1.3k 0.6× 1.1k 1.1× 394 0.6× 874 1.8× 375 1.2× 14 2.6k
Kenneth C. Keiler United States 27 2.4k 1.1× 1.2k 1.2× 680 1.1× 180 0.4× 213 0.7× 54 2.9k
Jan‐Willem De Gier Sweden 38 3.3k 1.5× 2.0k 1.9× 883 1.4× 263 0.5× 201 0.6× 68 4.2k

Countries citing papers authored by Gemma C. Atkinson

Since Specialization
Citations

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

Fields of papers citing papers by Gemma C. Atkinson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gemma C. Atkinson. 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 Gemma C. Atkinson. The network helps show where Gemma C. Atkinson may publish in the future.

Co-authorship network of co-authors of Gemma C. Atkinson

This figure shows the co-authorship network connecting the top 25 collaborators of Gemma C. Atkinson. A scholar is included among the top collaborators of Gemma C. Atkinson 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 Gemma C. Atkinson. Gemma C. Atkinson 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.
Tenson, Tanel, et al.. (2025). The Viral AlphaFold Database of monomers and homodimers reveals conserved protein folds in viruses of bacteria, archaea, and eukaryotes. Science Advances. 11(40). eadz8560–eadz8560. 2 indexed citations
2.
Egorov, Artyom A. & Gemma C. Atkinson. (2025). LoVis4u: a locus visualization tool for comparative genomics and coverage profiles. NAR Genomics and Bioinformatics. 7(1). lqaf009–lqaf009. 6 indexed citations
3.
Egorov, Artyom A., Alicia M. Cole, Toomas Mets, et al.. (2025). Characterization of five environmental phages infecting Escherichia coli K-12 isolated during a phage biology training course. Microbiology Spectrum. 13(12). e0227425–e0227425.
4.
Takada, Hiraku, Keigo Fujiwara, Gemma C. Atkinson, Shinobu Chiba, & Vasili Hauryliuk. (2024). Resolution of ribosomal stalling by EF-P and ABCF ATPases YfmR and YkpA/YbiT. Nucleic Acids Research. 52(16). 9854–9866. 9 indexed citations
5.
Svetlov, Maxim S., Gemma C. Atkinson, Haaris Ahsan Safdari, et al.. (2024). Peptidyl-tRNA hydrolase is the nascent chain release factor in bacterial ribosome-associated quality control. Molecular Cell. 84(4). 715–726.e5. 10 indexed citations
6.
Huang, Weiping, Elena V. Aleksandrova, Gemma C. Atkinson, et al.. (2024). Activity, structure, and diversity of Type II proline-rich antimicrobial peptides from insects. EMBO Reports. 25(11). 5194–5211. 5 indexed citations
7.
Tesson, Florian, Rémi Planel, Artyom A. Egorov, et al.. (2024). A Comprehensive Resource for Exploring Antiphage Defense: DefenseFinder Webservice,Wiki and Databases. SHILAP Revista de lepidopterología. 4. 27 indexed citations
8.
Takada, Hiraku, Gabriel Mazzucchelli, Iva Pichová, et al.. (2023). The structure of DarB in complex with Rel NTD reveals nonribosomal activation of Rel stringent factors. Science Advances. 9(3). eade4077–eade4077. 7 indexed citations
9.
Obana, Nozomu, Hiraku Takada, Caillan Crowe‐McAuliffe, et al.. (2023). Genome-encoded ABCF factors implicated in intrinsic antibiotic resistance in Gram-positive bacteria: VmlR2, Ard1 and CplR. Nucleic Acids Research. 51(9). 4536–4554. 16 indexed citations
10.
Egorov, Artyom A. & Gemma C. Atkinson. (2023). uORF4u: a tool for annotation of conserved upstream open reading frames. Bioinformatics. 39(5). 4 indexed citations
11.
Crowe‐McAuliffe, Caillan, Victoriia Murina, Kathryn Jane Turnbull, et al.. (2022). Structural basis for PoxtA-mediated resistance to phenicol and oxazolidinone antibiotics. Nature Communications. 13(1). 1860–1860. 41 indexed citations
12.
Kurata, Tatsuaki, Chayan Kumar Saha, Toomas Mets, et al.. (2022). A hyperpromiscuous antitoxin protein domain for the neutralization of diverse toxin domains. Proceedings of the National Academy of Sciences. 119(6). 22 indexed citations
13.
Tamman, Hedvig, Tatsuaki Kurata, Michele LeRoux, et al.. (2022). Direct activation of a bacterial innate immune system by a viral capsid protein. Nature. 612(7938). 132–140. 93 indexed citations
14.
Marks, James, Dorota Klepacki, Chayan Kumar Saha, et al.. (2022). Context-based sensing of orthosomycin antibiotics by the translating ribosome. Nature Chemical Biology. 18(11). 1277–1286. 6 indexed citations
15.
Tamman, Hedvig, Mohammad Roghanian, Ariel Talavera, et al.. (2022). Structure of SpoT reveals evolutionary tuning of catalysis via conformational constraint. Nature Chemical Biology. 19(3). 334–345. 8 indexed citations
16.
Svetlov, Maxim S., Egor A. Syroegin, Elena V. Aleksandrova, et al.. (2021). Structure of Erm-modified 70S ribosome reveals the mechanism of macrolide resistance. Nature Chemical Biology. 17(4). 412–420. 90 indexed citations
17.
Saha, Chayan Kumar, Tatsuaki Kurata, Sofia Raquel Alves Oliveira, et al.. (2020). A widespread toxin−antitoxin system exploiting growth control via alarmone signaling. Proceedings of the National Academy of Sciences. 117(19). 10500–10510. 74 indexed citations
18.
Kuzmenko, Anton, Stoyan Tankov, Gemma C. Atkinson, et al.. (2016). Aim-less translation: loss of Saccharomyces cerevisiae mitochondrial translation initiation factor mIF3/Aim23 leads to unbalanced protein synthesis. Scientific Reports. 6(1). 18749–18749. 22 indexed citations
19.
Kuzmenko, Anton, С. А. Левицкий, Gemma C. Atkinson, et al.. (2013). Protein biosynthesis in mitochondria. Biochemistry (Moscow). 78(8). 855–866. 11 indexed citations
20.
Atkinson, Gemma C. & Sandra L. Baldauf. (2010). Evolution of Elongation Factor G and the Origins of Mitochondrial and Chloroplast Forms. Molecular Biology and Evolution. 28(3). 1281–1292. 32 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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