Charles S. Bond

10.3k total citations · 1 hit paper
134 papers, 7.8k citations indexed

About

Charles S. Bond is a scholar working on Molecular Biology, Materials Chemistry and Epidemiology. According to data from OpenAlex, Charles S. Bond has authored 134 papers receiving a total of 7.8k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Molecular Biology, 28 papers in Materials Chemistry and 13 papers in Epidemiology. Recurrent topics in Charles S. Bond's work include RNA and protein synthesis mechanisms (30 papers), RNA Research and Splicing (27 papers) and Enzyme Structure and Function (24 papers). Charles S. Bond is often cited by papers focused on RNA and protein synthesis mechanisms (30 papers), RNA Research and Splicing (27 papers) and Enzyme Structure and Function (24 papers). Charles S. Bond collaborates with scholars based in Australia, United Kingdom and United States. Charles S. Bond's co-authors include Archa H. Fox, Ian Small, William N. Hunter, Alexander W. Schüttelkopf, Tetsuro Hirose, Shinichi Nakagawa, Sota Fujii, Gavin J. Knott, Alan H. Fairlamb and J.M. Guss and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Charles S. Bond

131 papers receiving 7.7k citations

Hit Papers

Functional Domains of NEAT1 Architectural lncRNA Induce P... 2018 2026 2020 2023 2018 100 200 300 400

Peers

Charles S. Bond
Joel P. Mackay Australia
Alper Küçükural United States
Florian Gnad Germany
Keith V. Wood United States
W. Andy Tao United States
Heng Zhu United States
Howard Riezman Switzerland
Ming‐Daw Tsai United States
Joel P. Mackay Australia
Charles S. Bond
Citations per year, relative to Charles S. Bond Charles S. Bond (= 1×) peers Joel P. Mackay

Countries citing papers authored by Charles S. Bond

Since Specialization
Citations

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

Fields of papers citing papers by Charles S. Bond

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles S. Bond. 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 Charles S. Bond. The network helps show where Charles S. Bond may publish in the future.

Co-authorship network of co-authors of Charles S. Bond

This figure shows the co-authorship network connecting the top 25 collaborators of Charles S. Bond. A scholar is included among the top collaborators of Charles S. Bond 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 Charles S. Bond. Charles S. Bond 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.
Ang, Ching‐Seng, Archa H. Fox, Anthony P. Duff, et al.. (2025). Structural dynamics of IDR interactions in human SFPQ and implications for liquid–liquid phase separation. Acta Crystallographica Section D Structural Biology. 81(7). 357–379. 1 indexed citations
2.
Kathman, Stefan G., Tao Liu, Charles S. Bond, et al.. (2025). NONO Maintains SREBP ‐Regulated Cholesterol Biosynthesis via RNA Binding in Neuroblastoma. The FASEB Journal. 39(18). e71051–e71051. 1 indexed citations
3.
Dennis, Michael, et al.. (2025). GRASP: a modular toolkit for building synthetic pentatricopeptide repeat RNA-binding proteins. Nucleic Acids Research. 53(20).
4.
Paudel, Bishnu P., Jason W. Schmidberger, Slobodan Jergic, et al.. (2024). Single-molecule visualization of sequence-specific RNA binding by a designer PPR protein. Nucleic Acids Research. 52(22). 14154–14170. 3 indexed citations
5.
Marshall, A.C., Gavin J. Knott, Timothy J. Ryan, et al.. (2024). Structural plasticity of the coiled–coil interactions in human SFPQ. Nucleic Acids Research. 53(2). 1 indexed citations
6.
Marshall, A.C., Simon Kobelke, Tianyi Zhu, et al.. (2023). Different Low-complexity Regions of SFPQ Play Distinct Roles in the Formation of Biomolecular Condensates. Journal of Molecular Biology. 435(24). 168364–168364. 13 indexed citations
7.
Debowski, Aleksandra W., David R. Thomas, Nichollas E. Scott, et al.. (2023). Macrophage infectivity potentiator protein, a peptidyl prolyl cis-trans isomerase, essential for Coxiella burnetii growth and pathogenesis. PLoS Pathogens. 19(7). e1011491–e1011491. 5 indexed citations
8.
Read, Randy J., Edward N. Baker, Charles S. Bond, Elspeth F. Garman, & Mark J. van Raaij. (2023). AlphaFold and the future of structural biology. Acta Crystallographica Section D Structural Biology. 79(7). 556–558. 6 indexed citations
9.
Haywood, Joel, et al.. (2022). A fungal tolerance trait and selective inhibitors proffer HMG-CoA reductase as a herbicide mode-of-action. Nature Communications. 13(1). 5563–5563. 15 indexed citations
10.
Knott, Gavin J., Daniel M. Passon, Xue‐hai Liang, et al.. (2021). Structural basis of dimerization and nucleic acid binding of human DBHS proteins NONO and PSPC1. Nucleic Acids Research. 50(1). 522–535. 23 indexed citations
11.
Meng, Yongjie, Muhammad Kamran, Marion Dalmais, et al.. (2021). KARRIKIN INSENSITIVE2 regulates leaf development, root system architecture and arbuscular‐mycorrhizal symbiosis in Brachypodium distachyon. The Plant Journal. 109(6). 1559–1574. 21 indexed citations
12.
Schmidberger, Jason W., Katie A. Wilson, Cameron W. Evans, et al.. (2020). High resolution crystal structure of a KRAS promoter G-quadruplex reveals a dimer with extensive poly-A π-stacking interactions for small-molecule recognition. Nucleic Acids Research. 48(10). 5766–5776. 32 indexed citations
13.
Spackman, Peter R., Li‐Juan Yu, Craig J. Morton, et al.. (2019). Bridging Crystal Engineering and Drug Discovery by Utilizing Intermolecular Interactions and Molecular Shapes in Crystals. Angewandte Chemie International Edition. 58(47). 16780–16784. 34 indexed citations
14.
Yamazaki, Tomohiro, Sylvie Souquère, Takeshi Chujo, et al.. (2018). Functional Domains of NEAT1 Architectural lncRNA Induce Paraspeckle Assembly through Phase Separation. Molecular Cell. 70(6). 1038–1053.e7. 422 indexed citations breakdown →
15.
Gully, Benjamin S., Nathan Cowieson, Will A. Stanley, et al.. (2015). The solution structure of the pentatricopeptide repeat protein PPR10 upon binding atpH RNA. Nucleic Acids Research. 43(3). 1918–1926. 55 indexed citations
16.
Bond, Charles S., et al.. (2014). Try This Crystal Building. Teaching science (Deakin West, A.C.T. : Online)/Teaching science. 60(2). 14. 1 indexed citations
17.
Scaffidi, Adrian, Mark T. Waters, Brian W. Skelton, et al.. (2012). Solar irradiation of the seed germination stimulant karrikinolide produces two novel head-to-head cage dimers. Organic & Biomolecular Chemistry. 10(20). 4069–4069. 7 indexed citations
18.
Bond, Charles S., et al.. (2003). Structure of a tetragonal crystal form ofEscherichia coli2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase. Acta Crystallographica Section D Biological Crystallography. 59(3). 607–610. 29 indexed citations
19.
Bond, Charles S., Yihong Zhang, Matthew Berriman, et al.. (1999). Crystal structure of Trypanosoma cruzi trypanothione reductase in complex with trypanothione, and the structure-based discovery of new natural product inhibitors. Structure. 7(1). 81–89. 173 indexed citations
20.
Bond, Charles S., et al.. (1997). Structure of a human lysosomal sulfatase. Structure. 5(2). 277–289. 251 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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