John F. Atkins

21.5k total citations · 3 hit papers
290 papers, 16.2k citations indexed

About

John F. Atkins is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, John F. Atkins has authored 290 papers receiving a total of 16.2k indexed citations (citations by other indexed papers that have themselves been cited), including 206 papers in Molecular Biology, 57 papers in Genetics and 49 papers in Ecology. Recurrent topics in John F. Atkins's work include RNA and protein synthesis mechanisms (167 papers), RNA modifications and cancer (73 papers) and Bacteriophages and microbial interactions (47 papers). John F. Atkins is often cited by papers focused on RNA and protein synthesis mechanisms (167 papers), RNA modifications and cancer (73 papers) and Bacteriophages and microbial interactions (47 papers). John F. Atkins collaborates with scholars based in United States, Ireland and United Kingdom. John F. Atkins's co-authors include Raymond F. Gesteland, Andrew E. Firth, R.F. Gesteland, Pavel V. Baranov, Norma M. Wills, Robert B. Weiss, Betty Chung, Ivaylo P. Ivanov, Carl W. Anderson and Gary Loughran and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

John F. Atkins

284 papers receiving 15.5k citations

Hit Papers

An overlapping essential gene in the Potyviridae 2008 2026 2014 2020 2008 2012 2021 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John F. Atkins United States 71 11.1k 3.0k 2.3k 2.0k 1.4k 290 16.2k
Hugh R.B. Pelham United Kingdom 80 20.7k 1.9× 2.1k 0.7× 2.6k 1.1× 1.5k 0.7× 710 0.5× 133 26.7k
John J. Dunn United States 43 10.8k 1.0× 4.7k 1.6× 1.3k 0.6× 3.0k 1.5× 1.8k 1.2× 98 15.9k
S Inouye Japan 61 8.8k 0.8× 2.2k 0.7× 1.4k 0.6× 1.1k 0.5× 1.3k 0.9× 337 13.6k
Walter Fiers Belgium 79 13.5k 1.2× 3.6k 1.2× 1.3k 0.6× 3.2k 1.6× 1.8k 1.2× 308 27.5k
Henry D. Hunt United States 30 7.2k 0.6× 2.0k 0.7× 1.1k 0.5× 698 0.3× 763 0.5× 73 12.1k
Charles Weissmann Switzerland 81 22.5k 2.0× 3.6k 1.2× 1.3k 0.5× 1.7k 0.8× 1.1k 0.8× 216 28.5k
David F. Smith United States 68 12.9k 1.2× 2.4k 0.8× 587 0.3× 822 0.4× 1.0k 0.7× 215 17.2k
Robert M. Horton United States 22 7.8k 0.7× 2.0k 0.7× 1.1k 0.5× 793 0.4× 770 0.5× 64 12.6k
Aaron J. Shatkin United States 68 11.0k 1.0× 3.1k 1.1× 1.4k 0.6× 2.0k 1.0× 3.6k 2.5× 197 15.4k
John M. Taylor United States 79 8.6k 0.8× 2.1k 0.7× 1.2k 0.5× 708 0.4× 2.4k 1.7× 286 19.4k

Countries citing papers authored by John F. Atkins

Since Specialization
Citations

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

Fields of papers citing papers by John F. Atkins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John F. Atkins

This figure shows the co-authorship network connecting the top 25 collaborators of John F. Atkins. A scholar is included among the top collaborators of John F. Atkins 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 John F. Atkins. John F. Atkins 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.
Vallesi, Adriana, et al.. (2023). Nontriplet feature of genetic code in Euplotes ciliates is a result of neutral evolution. Proceedings of the National Academy of Sciences. 120(22). e2221683120–e2221683120. 12 indexed citations
2.
Vila‐Sanjurjo, Antón, Natalia Mallo, John F. Atkins, Joanna L. Elson, & Paul Smith. (2023). Our current understanding of the toxicity of altered mito-ribosomal fidelity during mitochondrial protein synthesis: What can it tell us about human disease?. Frontiers in Physiology. 14. 1082953–1082953. 4 indexed citations
3.
Fromm, Simon A., Michael D. Purdy, Pramod R. Bhatt, et al.. (2023). The translating bacterial ribosome at 1.55 Å resolution generated by cryo-EM imaging services. Nature Communications. 14(1). 1095–1095. 28 indexed citations
4.
Hudson, Andrew M., et al.. (2021). Tissue-specific dynamic codon redefinition in Drosophila. Proceedings of the National Academy of Sciences. 118(5). 10 indexed citations
5.
Bhatt, Pramod R., Alain Scaiola, Gary Loughran, et al.. (2021). Structural basis of ribosomal frameshifting during translation of the SARS-CoV-2 RNA genome. Science. 372(6548). 1306–1313. 176 indexed citations breakdown →
6.
Loughran, Gary, Alexander V. Zhdanov, Sergey I. Kovalchuk, et al.. (2020). Unusually efficient CUG initiation of an overlapping reading frame in POLG mRNA yields novel protein POLGARF. Proceedings of the National Academy of Sciences. 117(40). 24936–24946. 26 indexed citations
7.
Antonov, Ivan, et al.. (2013). Identification of the nature of reading frame transitions observed in prokaryotic genomes. Nucleic Acids Research. 41(13). 6514–6530. 24 indexed citations
8.
Atkins, John F., Raymond F. Gesteland, & Thomas R. Cech. (2011). RNA worlds : from life's origins to diversity in gene regulation. 84 indexed citations
10.
Lao, Nga T., Alan P. Maloney, John F. Atkins, & Tony A. Kavanagh. (2009). Versatile Dual Reporter Gene Systems for Investigating Stop Codon Readthrough in Plants. PLoS ONE. 4(10). e7354–e7354. 8 indexed citations
11.
Chung, Betty, W. Allen Miller, John F. Atkins, & Andrew E. Firth. (2008). An overlapping essential gene in the Potyviridae. Proceedings of the National Academy of Sciences. 105(15). 5897–5902. 711 indexed citations breakdown →
12.
Wills, Norma M., et al.. (2008). Translational bypassing without peptidyl‐tRNA anticodon scanning of coding gap mRNA. The EMBO Journal. 27(19). 2533–2544. 22 indexed citations
13.
Atkins, John F., Raymond F. Gesteland, Richard J. Jackson, & Norma M. Wills. (2006). 16 The Shapely mRNA: Knotting Ventured, Knotting Gained. Cold Spring Harbor Monograph Archive. 43. 437–467. 4 indexed citations
14.
Zhang, Yan, Pavel V. Baranov, John F. Atkins, & Vadim N. Gladyshev. (2005). Pyrrolysine and Selenocysteine Use Dissimilar Decoding Strategies. Journal of Biological Chemistry. 280(21). 20740–20751. 91 indexed citations
15.
Baranov, Pavel V., Raymond F. Gesteland, & John F. Atkins. (2004). P-site tRNA is a crucial initiator of ribosomal frameshifting. RNA. 10(2). 221–230. 70 indexed citations
16.
Atkins, John F., August Böck, Senya Matsufuji, & Raymond F. Gesteland. (1999). 24 Dynamics of the Genetic Code. Cold Spring Harbor Monograph Archive. 37. 637–673. 14 indexed citations
17.
Choi, Kyoung Moo, John F. Atkins, Raymond F. Gesteland, & Richard Brimacombe. (1998). Flexibility of the nascent polypeptide chain within the ribosome. European Journal of Biochemistry. 255(2). 409–413. 26 indexed citations
18.
Gesteland, Raymond F. & John F. Atkins. (1993). The RNA world : the nature of modern RNA suggests a prebiotic RNA world. 207 indexed citations
19.
Condron, Barry, Raymond F. Gesteland, & John F. Atkins. (1991). An analysis of sequences stimulating frameshifting in the decoding of gene 10 of bacteriophage T7. Nucleic Acids Research. 19(20). 5607–5612. 38 indexed citations
20.
Atkins, John F.. (1980). Nontriplet tRNA–mRNA Interactions. Cold Spring Harbor Monograph Archive. 439–449. 3 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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