Jonathan A. King

1.7k total citations
25 papers, 1.3k citations indexed

About

Jonathan A. King is a scholar working on Molecular Biology, Ecology and Structural Biology. According to data from OpenAlex, Jonathan A. King has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 11 papers in Ecology and 4 papers in Structural Biology. Recurrent topics in Jonathan A. King's work include Bacteriophages and microbial interactions (10 papers), Microbial Community Ecology and Physiology (6 papers) and Heat shock proteins research (6 papers). Jonathan A. King is often cited by papers focused on Bacteriophages and microbial interactions (10 papers), Microbial Community Ecology and Physiology (6 papers) and Heat shock proteins research (6 papers). Jonathan A. King collaborates with scholars based in United States, Japan and Mexico. Jonathan A. King's co-authors include Cameron Haase‐Pettingell, Wah Chiu, Daniel Blankschtein, Daniel T. Kamei, Daniel I. C. Wang, Michael F. Schmid, Wen Jiang, Joanita Jakana, Corey F. Hryc and Melissa S. Kosinski‐Collins and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Jonathan A. King

25 papers receiving 1.3k 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 A. King United States 22 947 368 208 170 147 25 1.3k
Cameron Haase‐Pettingell United States 23 1.3k 1.3× 519 1.4× 342 1.6× 152 0.9× 191 1.3× 35 1.7k
Nelly R. Hajizadeh Germany 7 1.3k 1.4× 107 0.3× 528 2.5× 19 0.1× 169 1.1× 10 1.9k
Dmitri N. Ermolenko United States 25 2.5k 2.6× 188 0.5× 297 1.4× 33 0.2× 394 2.7× 49 2.7k
Melissa A. Graewert Germany 16 896 0.9× 77 0.2× 505 2.4× 33 0.2× 52 0.4× 34 1.4k
Irina A. Shkel United States 18 1.0k 1.1× 144 0.4× 228 1.1× 9 0.1× 279 1.9× 34 1.4k
Andrey Gruzinov Russia 11 568 0.6× 57 0.2× 269 1.3× 17 0.1× 46 0.3× 26 983
Jorge Alegre‐Cebollada Spain 25 1.1k 1.2× 79 0.2× 126 0.6× 49 0.3× 143 1.0× 54 2.1k
Anne Tuukkanen Germany 19 1.2k 1.3× 92 0.3× 402 1.9× 10 0.1× 202 1.4× 25 1.7k
Daouda A. K. Traoré Australia 17 553 0.6× 54 0.1× 125 0.6× 21 0.1× 124 0.8× 40 1.1k
Vincent L. G. Postis United Kingdom 16 908 1.0× 47 0.1× 75 0.4× 47 0.3× 117 0.8× 34 1.3k

Countries citing papers authored by Jonathan A. King

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan A. King

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan A. King

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan A. King. A scholar is included among the top collaborators of Jonathan A. King 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 A. King. Jonathan A. King 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.
Kosinski‐Collins, Melissa S., et al.. (2019). Kinetic Stability of Long-Lived Human Lens γ-Crystallins and Their Isolated Double Greek Key Domains. Biophysical Journal. 117(2). 269–280. 21 indexed citations
2.
Dai, Wei, Muyuan Chen, Christopher G. Myers, et al.. (2018). Visualizing Individual RuBisCO and Its Assembly into Carboxysomes in Marine Cyanobacteria by Cryo-Electron Tomography. Journal of Molecular Biology. 430(21). 4156–4167. 46 indexed citations
3.
Hryc, Corey F., Donghua Chen, Pavel V. Afonine, et al.. (2017). Accurate model annotation of a near-atomic resolution cryo-EM map. Proceedings of the National Academy of Sciences. 114(12). 3103–3108. 87 indexed citations
4.
Pintilie, Grigore, Donghua Chen, Cameron Haase‐Pettingell, Jonathan A. King, & Wah Chiu. (2015). Resolution and Probabilistic Models of Components in CryoEM Maps of Mature P22 Bacteriophage. Biophysical Journal. 110(4). 827–839. 32 indexed citations
5.
Darrow, Michele C., Oksana A. Sergeeva, J. Mario Isas, et al.. (2015). Structural Mechanisms of Mutant Huntingtin Aggregation Suppression by the Synthetic Chaperonin-like CCT5 Complex Explained by Cryoelectron Tomography. Journal of Biological Chemistry. 290(28). 17451–17461. 30 indexed citations
6.
Baker, Matthew L., et al.. (2014). Protruding knob-like proteins violate local symmetries in an icosahedral marine virus. Nature Communications. 5(1). 4278–4278. 21 indexed citations
7.
Chiu, Wah, Wei Dai, Caroline Fu, et al.. (2014). Visualizing Virus Assembly Intermediates Inside Marine Cyanobacteria by Zernike Phase Contrast Electron Cryo-Tomography. Microscopy and Microanalysis. 20(S3). 202–203. 2 indexed citations
8.
Sergeeva, Oksana A., et al.. (2013). Human CCT4 and CCT5 Chaperonin Subunits Expressed in Escherichia coli Form Biologically Active Homo-oligomers. Journal of Biological Chemistry. 288(24). 17734–17744. 51 indexed citations
9.
Dai, Wei, Caroline Fu, John M. Flanagan, et al.. (2013). Visualizing virus assembly intermediates inside marine cyanobacteria. Nature. 502(7473). 707–710. 104 indexed citations
10.
Zhu, Bin, et al.. (2012). The RNA Polymerase of Marine Cyanophage Syn5. Journal of Biological Chemistry. 288(5). 3545–3552. 24 indexed citations
11.
12.
Baker, Matthew L., Corey F. Hryc, Frank DiMaio, et al.. (2011). Structural basis for scaffolding-mediated assembly and maturation of a dsDNA virus. Proceedings of the National Academy of Sciences. 108(4). 1355–1360. 173 indexed citations
13.
Schmid, Michael F., et al.. (2010). Visualizing the Structural Changes of Bacteriophage Epsilon15 and Its Salmonella Host during Infection. Journal of Molecular Biology. 402(4). 731–740. 59 indexed citations
14.
Das, Payel, Jonathan A. King, & Ruhong Zhou. (2009). β‐strand interactions at the domain interface critical for the stability of human lens γD‐crystallin. Protein Science. 19(1). 131–140. 47 indexed citations
15.
Flaugh, Shannon L., et al.. (2007). Folding and stability of the isolated Greek key domains of the long‐lived human lens proteins γD‐crystallin and γS‐crystallin. Protein Science. 16(11). 2427–2444. 92 indexed citations
16.
Kamei, Daniel T., Jonathan A. King, Daniel I. C. Wang, & Daniel Blankschtein. (2002). Separating lysozyme from bacteriophage P22 in two‐phase aqueous micellar systems. Biotechnology and Bioengineering. 80(2). 233–236. 37 indexed citations
17.
Kamei, Daniel T., et al.. (2002). Understanding viral partitioning in two‐phase aqueous nonionic micellar systems: 1. Role of attractive interactions between viruses and micelles. Biotechnology and Bioengineering. 78(2). 190–202. 27 indexed citations
18.
Kamei, Daniel T., Jonathan A. King, Daniel I. C. Wang, & Daniel Blankschtein. (2002). Understanding viral partitioning in two‐phase aqueous nonionic micellar systems: 2. Effect of entrained micelle‐poor domains. Biotechnology and Bioengineering. 78(2). 203–216. 32 indexed citations
19.
Kamei, Daniel T., et al.. (1998). Separation of proteins and viruses using two-phase aqueous micellar systems. Journal of Chromatography B Biomedical Sciences and Applications. 711(1-2). 127–138. 129 indexed citations
20.
Smith, Albert V., Jonathan A. King, & Terry L. Orr‐Weaver. (1993). Identification of genomic regions required for DNA replication during Drosophila embryogenesis.. Genetics. 135(3). 817–829. 29 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Cameron Haase‐Pettingell Breakdown of academic impact, for papers by Nelly R. Hajizadeh Breakdown of academic impact, for papers by Dmitri N. Ermolenko Breakdown of academic impact, for papers by Melissa A. Graewert Breakdown of academic impact, for papers by Irina A. Shkel Breakdown of academic impact, for papers by Andrey Gruzinov Breakdown of academic impact, for papers by Jorge Alegre‐Cebollada Breakdown of academic impact, for papers by Anne Tuukkanen Breakdown of academic impact, for papers by Daouda A. K. Traoré Breakdown of academic impact, for papers by Vincent L. G. Postis
Rankless by CCL
2026