Elizabeth M. Fozo

2.1k total citations
33 papers, 1.7k citations indexed

About

Elizabeth M. Fozo is a scholar working on Molecular Biology, Ecology and Genetics. According to data from OpenAlex, Elizabeth M. Fozo has authored 33 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Ecology and 14 papers in Genetics. Recurrent topics in Elizabeth M. Fozo's work include Bacteriophages and microbial interactions (15 papers), Bacterial Genetics and Biotechnology (14 papers) and RNA and protein synthesis mechanisms (9 papers). Elizabeth M. Fozo is often cited by papers focused on Bacteriophages and microbial interactions (15 papers), Bacterial Genetics and Biotechnology (14 papers) and RNA and protein synthesis mechanisms (9 papers). Elizabeth M. Fozo collaborates with scholars based in United States, United Kingdom and Germany. Elizabeth M. Fozo's co-authors include Robert G. Quivey, Gisela Storz, Matthew R. Hemm, Jessica K. Kajfasz, Natalya Yutin, Kira S. Makarova, Svetlana A. Shabalina, Eugene V. Koonin, Jason A. Opdyke and Virginia L. Clark and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Elizabeth M. Fozo

32 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth M. Fozo United States 21 874 612 527 268 231 33 1.7k
Josephine R. Chandler United States 24 1.3k 1.5× 397 0.6× 263 0.5× 287 1.1× 135 0.6× 41 2.1k
Nathalie Leblond‐Bourget France 21 973 1.1× 291 0.5× 331 0.6× 290 1.1× 564 2.4× 47 1.7k
Sarah Dubrac France 22 1.2k 1.4× 684 1.1× 304 0.6× 726 2.7× 175 0.8× 32 1.9k
Xhavit Zogaj United States 12 1.1k 1.2× 327 0.5× 313 0.6× 130 0.5× 304 1.3× 15 1.8k
Christopher J. Kristich United States 26 1.3k 1.5× 485 0.8× 240 0.5× 1.0k 3.8× 379 1.6× 53 2.3k
Saulius Kulakauskas France 29 1.4k 1.6× 375 0.6× 449 0.9× 197 0.7× 824 3.6× 53 2.3k
Damien Balestrino France 24 1.7k 1.9× 466 0.8× 478 0.9× 265 1.0× 555 2.4× 34 2.7k
Raquel Tobes Spain 19 1.3k 1.5× 569 0.9× 279 0.5× 297 1.1× 160 0.7× 42 2.2k
Pavel Branny Czechia 22 869 1.0× 458 0.7× 193 0.4× 227 0.8× 115 0.5× 45 1.5k
Jetta J. E. Bijlsma Netherlands 28 907 1.0× 413 0.7× 217 0.4× 276 1.0× 353 1.5× 45 2.3k

Countries citing papers authored by Elizabeth M. Fozo

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth M. Fozo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth M. Fozo

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth M. Fozo. A scholar is included among the top collaborators of Elizabeth M. Fozo 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 Elizabeth M. Fozo. Elizabeth M. Fozo 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.
Johnston, R. D., et al.. (2025). Unexpected contribution of the Fak system and the thioesterase TesE to the growth and membrane physiology of Enterococcus faecalis. Journal of Bacteriology. 207(7). e0012125–e0012125. 1 indexed citations
2.
Fozo, Elizabeth M., et al.. (2024). Type I toxin-antitoxin systems in bacteria: from regulation to biological functions. EcoSal Plus. 12(1). eesp00252022–eesp00252022. 8 indexed citations
3.
Dhowlaghar, Nitin, Lauren K. Hudson, Daniel W. Bryan, et al.. (2023). Selection of mutant Listeria phages under food-relevant conditions can enhance application potential. Applied and Environmental Microbiology. 89(10). e0100723–e0100723. 2 indexed citations
4.
Fozo, Elizabeth M., et al.. (2023). Dual stable isotopes enhance lipidomic studies in bacterial model organism Enterococcus faecalis. Analytical and Bioanalytical Chemistry. 415(17). 3593–3605. 6 indexed citations
5.
Fozo, Elizabeth M., et al.. (2022). Charged Amino Acids Contribute to ZorO Toxicity. Toxins. 15(1). 32–32. 5 indexed citations
6.
Campagna, Shawn R., et al.. (2021). Enterococcus faecalis Readily Adapts Membrane Phospholipid Composition to Environmental and Genetic Perturbation. Frontiers in Microbiology. 12. 616045–616045. 18 indexed citations
7.
8.
Fozo, Elizabeth M., et al.. (2019). Second Harmonic Generation Spectroscopy of Membrane Probe Dynamics in Gram-Positive Bacteria. Biophysical Journal. 117(8). 1419–1428. 23 indexed citations
9.
Martin, Robbie M., Stephen P. Dearth, Gary R. LeCleir, et al.. (2017). Microcystin-LR does not induce alterations to transcriptomic or metabolomic profiles of a model heterotrophic bacterium. PLoS ONE. 12(12). e0189608–e0189608. 5 indexed citations
10.
Fozo, Elizabeth M., et al.. (2017). Enterococcus faecalis Responds to Individual Exogenous Fatty Acids Independently of Their Degree of Saturation or Chain Length. Applied and Environmental Microbiology. 84(1). 26 indexed citations
11.
Fozo, Elizabeth M., et al.. (2016). The 5΄ UTR of the type I toxin ZorO can both inhibit and enhance translation. Nucleic Acids Research. 45(7). 4006–4020. 22 indexed citations
12.
Fozo, Elizabeth M. & Elizabeth A. Rucks. (2016). The Making and Taking of Lipids. Advances in microbial physiology. 69. 51–155. 34 indexed citations
13.
Fozo, Elizabeth M.. (2012). New type I toxin-antitoxin families from “wild” and laboratory strains ofE. coli. RNA Biology. 9(12). 1504–1512. 41 indexed citations
14.
Opdyke, Jason A., Elizabeth M. Fozo, Matthew R. Hemm, & Gisela Storz. (2010). RNase III Participates in GadY-Dependent Cleavage of the gadX-gadW mRNA. Journal of Molecular Biology. 406(1). 29–43. 86 indexed citations
15.
Fozo, Elizabeth M., Kira S. Makarova, Svetlana A. Shabalina, et al.. (2010). Abundance of type I toxin–antitoxin systems in bacteria: searches for new candidates and discovery of novel families. Nucleic Acids Research. 38(11). 3743–3759. 212 indexed citations
16.
Fozo, Elizabeth M., Mitsuoki Kawano, Fanette Fontaine, et al.. (2008). Repression of small toxic protein synthesis by the Sib and OhsC small RNAs. Molecular Microbiology. 70(5). 1076–1093. 134 indexed citations
17.
Fozo, Elizabeth M. & Robert G. Quivey. (2004). Shifts in the Membrane Fatty Acid Profile ofStreptococcus mutansEnhance Survival in Acidic Environments. Applied and Environmental Microbiology. 70(2). 929–936. 171 indexed citations
18.
Fozo, Elizabeth M. & Robert G. Quivey. (2004). The fabM Gene Product of Streptococcus mutans Is Responsible for the Synthesis of Monounsaturated Fatty Acids and Is Necessary for Survival at Low pH. Journal of Bacteriology. 186(13). 4152–4158. 101 indexed citations
19.
Fozo, Elizabeth M., et al.. (2004). Low pH-induced membrane fatty acid alterations in oral bacteria. FEMS Microbiology Letters. 238(2). 291–295. 100 indexed citations
20.
Fozo, Elizabeth M., et al.. (2000). Gonococcal Nitric Oxide Reductase Is Encoded by a Single Gene, norB , Which Is Required for Anaerobic Growth and Is Induced by Nitric Oxide. Infection and Immunity. 68(9). 5241–5246. 83 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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