Jeffrey M. Boyd

20.5k total citations
88 papers, 2.5k citations indexed

About

Jeffrey M. Boyd is a scholar working on Molecular Biology, Infectious Diseases and Renewable Energy, Sustainability and the Environment. According to data from OpenAlex, Jeffrey M. Boyd has authored 88 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 28 papers in Infectious Diseases and 19 papers in Renewable Energy, Sustainability and the Environment. Recurrent topics in Jeffrey M. Boyd's work include Antimicrobial Resistance in Staphylococcus (27 papers), Bacterial biofilms and quorum sensing (23 papers) and Trace Elements in Health (17 papers). Jeffrey M. Boyd is often cited by papers focused on Antimicrobial Resistance in Staphylococcus (27 papers), Bacterial biofilms and quorum sensing (23 papers) and Trace Elements in Health (17 papers). Jeffrey M. Boyd collaborates with scholars based in United States, United Kingdom and Australia. Jeffrey M. Boyd's co-authors include Ameya A. Mashruwala, Diana M. Downs, Eric S. Boyd, Faina Bogomolniy, M.G. Federici, Esther Rhei, Patrick I. Borgen, Lan Kang, Adriana van de Guchte and Scott A. Ensign and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Jeffrey M. Boyd

83 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey M. Boyd United States 30 1.5k 566 433 315 224 88 2.5k
Jin‐Won Lee South Korea 22 1.1k 0.7× 172 0.3× 287 0.7× 403 1.3× 338 1.5× 71 2.5k
Marcus Miethke Germany 24 1.6k 1.0× 256 0.5× 199 0.5× 735 2.3× 251 1.1× 37 3.3k
Laura Baldomà Spain 37 2.4k 1.6× 301 0.5× 79 0.2× 571 1.8× 467 2.1× 115 4.2k
Jonathan W. Olson United States 22 535 0.3× 207 0.4× 288 0.7× 80 0.3× 313 1.4× 35 1.8k
Mohammad Saeid Hejazi Iran 37 2.1k 1.3× 321 0.6× 129 0.3× 118 0.4× 126 0.6× 140 3.6k
Emile Schiltz Germany 32 1.8k 1.2× 130 0.2× 165 0.4× 424 1.3× 346 1.5× 66 2.7k
Danièle Touati France 19 1.0k 0.7× 103 0.2× 128 0.3× 461 1.5× 289 1.3× 24 2.5k
Stephen P. Kidd Australia 29 969 0.6× 370 0.7× 62 0.1× 286 0.9× 177 0.8× 86 2.6k
Francisco Rodríguez‐Quiñones United Kingdom 9 1.1k 0.7× 165 0.3× 145 0.3× 684 2.2× 221 1.0× 14 2.8k
Mark R. O’Brian United States 35 1.4k 0.9× 101 0.2× 149 0.3× 219 0.7× 151 0.7× 81 3.0k

Countries citing papers authored by Jeffrey M. Boyd

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey M. Boyd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey M. Boyd. 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 Jeffrey M. Boyd. The network helps show where Jeffrey M. Boyd may publish in the future.

Co-authorship network of co-authors of Jeffrey M. Boyd

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey M. Boyd. A scholar is included among the top collaborators of Jeffrey M. Boyd 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 Jeffrey M. Boyd. Jeffrey M. Boyd 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
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Boyd, Jeffrey M., Mary E. Foley, Timothy G. Stephens, et al.. (2024). Fpa (YlaN) is an iron(II) binding protein that functions to relieve Fur-mediated repression of gene expression in Staphylococcus aureus. mBio. 15(11). e0231024–e0231024. 4 indexed citations
4.
Morey, Jacqueline R., Stephanie L. Neville, Katherine Ganio, et al.. (2023). Host subversion of bacterial metallophore usage drives copper intoxication. mBio. 14(5). e0135023–e0135023. 8 indexed citations
6.
Kim, Ji‐Sun, et al.. (2023). Impact of the pentose phosphate pathway on metabolism and pathogenesis of Staphylococcus aureus. PLoS Pathogens. 19(7). e1011531–e1011531. 23 indexed citations
7.
Leanse, Leon G., Carolina dos Anjos, Jie Hui, et al.. (2023). Blue Light Potentiates Antibiotics in Bacteria via Parallel Pathways of Hydroxyl Radical Production and Enhanced Antibiotic Uptake. Advanced Science. 10(36). e2303731–e2303731. 8 indexed citations
8.
Rudra, Paulami, et al.. (2021). Tools, Strains, and Strategies To Effectively Conduct Anaerobic and Aerobic Transcriptional Reporter Screens and Assays in Staphylococcus aureus. Applied and Environmental Microbiology. 87(21). e0110821–e0110821. 4 indexed citations
9.
Huh, Hyun, et al.. (2021). Impact of FtsZ Inhibition on the Localization of the Penicillin Binding Proteins in Methicillin-Resistant Staphylococcus aureus. Journal of Bacteriology. 203(16). e0020421–e0020421. 18 indexed citations
10.
Hooven, Thomas A., et al.. (2021). Growth and Stress Tolerance Comprise Independent Metabolic Strategies Critical for Staphylococcus aureus Infection. mBio. 12(3). e0081421–e0081421. 18 indexed citations
11.
Miguel-Romero, Laura, Katarina Kulhánková, Michael P. Cahill, et al.. (2020). The SrrAB two-component system regulates Staphylococcus aureus pathogenicity through redox sensitive cysteines. Proceedings of the National Academy of Sciences. 117(20). 10989–10999. 58 indexed citations
12.
Boyd, Jeffrey M., et al.. (2020). Genetic Regulation of Metal Ion Homeostasis in Staphylococcus aureus. Trends in Microbiology. 28(10). 821–831. 37 indexed citations
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Mashruwala, Ameya A., et al.. (2019). Drug-like Fragments Inhibit agr-Mediated Virulence Expression in Staphylococcus aureus. Scientific Reports. 9(1). 6786–6786. 30 indexed citations
14.
Mashruwala, Ameya A. & Jeffrey M. Boyd. (2017). Investigating the role(s) of SufT and the domain of unknown function 59 (DUF59) in the maturation of iron–sulfur proteins. Current Genetics. 64(1). 9–16. 14 indexed citations
15.
Mashruwala, Ameya A. & Jeffrey M. Boyd. (2015). De Novo Assembly of Plasmids Using Yeast Recombinational Cloning. Methods in molecular biology. 1373. 33–41. 14 indexed citations
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Boyd, Jeffrey M., et al.. (2015). Physiological roles of bacillithiol in intracellular metal processing. Current Genetics. 62(1). 59–65. 29 indexed citations
17.
Perrineau, Marie‐Mathilde, Ehud Zelzion, Jeferson Gross, et al.. (2013). Evolution of salt tolerance in a laboratory reared population of C hlamydomonas reinhardtii. Environmental Microbiology. 16(6). 1755–1766. 87 indexed citations
18.
Boyd, Jeffrey M. & Scott A. Ensign. (2005). ATP-Dependent Enolization of Acetone by Acetone Carboxylase from Rhodobacter capsulatus. Biochemistry. 44(23). 8543–8553. 19 indexed citations
19.
Boyd, Jeffrey M., et al.. (2004). Bacterial Acetone Carboxylase Is a Manganese-dependent Metalloenzyme. Journal of Biological Chemistry. 279(45). 46644–46651. 27 indexed citations
20.
Boyd, Jeffrey M., et al.. (1963). Platelet Adherence to Polymorphs. BMJ. 2(5359). 747.1–747. 9 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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