Matthew C. Radey

5.0k total citations · 2 hit papers
41 papers, 2.4k citations indexed

About

Matthew C. Radey is a scholar working on Molecular Biology, Endocrinology and Infectious Diseases. According to data from OpenAlex, Matthew C. Radey has authored 41 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Endocrinology and 8 papers in Infectious Diseases. Recurrent topics in Matthew C. Radey's work include Vibrio bacteria research studies (10 papers), Gut microbiota and health (8 papers) and Antibiotic Resistance in Bacteria (7 papers). Matthew C. Radey is often cited by papers focused on Vibrio bacteria research studies (10 papers), Gut microbiota and health (8 papers) and Antibiotic Resistance in Bacteria (7 papers). Matthew C. Radey collaborates with scholars based in United States, France and United Kingdom. Matthew C. Radey's co-authors include Joseph D. Mougous, M. Brittnacher, Hillary S. Hayden, S. Brook Peterson, Elhanan Borenstein, Dustin E. Bosch, Samuel I. Miller, FoSheng Hsu, Jun Zeng and Marcos H. de Moraes and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Matthew C. Radey

39 papers receiving 2.4k citations

Hit Papers

A bacterial cytidine deaminase toxin enables CRISPR-free ... 2020 2026 2022 2024 2020 2023 100 200 300 400

Peers

Matthew C. Radey
Ajai A. Dandekar United States
Weihui Wu China
Tami D. Lieberman United States
F. Heath Damron United States
Biswa Choudhury United States
Matthew C. Radey
Citations per year, relative to Matthew C. Radey Matthew C. Radey (= 1×) peers Anders Folkesson

Countries citing papers authored by Matthew C. Radey

Since Specialization
Citations

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

Fields of papers citing papers by Matthew C. Radey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew C. Radey. 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 Matthew C. Radey. The network helps show where Matthew C. Radey may publish in the future.

Co-authorship network of co-authors of Matthew C. Radey

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew C. Radey. A scholar is included among the top collaborators of Matthew C. Radey 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 Matthew C. Radey. Matthew C. Radey 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.
Ratner, Hannah K., et al.. (2025). An electron transport complex required in the gut sensitizes Bacteroides to a pore-forming type VI secretion toxin. Proceedings of the National Academy of Sciences. 122(50). e2523503122–e2523503122. 1 indexed citations
2.
Kapnadak, Siddhartha G., Matthew C. Radey, M. Teresi, et al.. (2023). 57 Bronchoscopy sampling finds that intra-lung bacterial migration contributes to persistent Pseudomonas aeruginosa infection after elexacaftor-tezacaftor-ivacaftor. Journal of Cystic Fibrosis. 22. S31–S31.
3.
Gallagher, Larry A., Andi Liu, Ian R. Humphreys, et al.. (2023). Genetic manipulation of Patescibacteria provides mechanistic insights into microbial dark matter and the epibiotic lifestyle. Cell. 186(22). 4803–4817.e13. 52 indexed citations breakdown →
4.
Hayden, Hillary S., Snehal Joshi, Matthew C. Radey, et al.. (2022). Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human Infections. mBio. 13(5). e0142422–e0142422. 4 indexed citations
5.
LaCourse, Kaitlyn D., Hannah E. Ledvina, Rutan Zhang, et al.. (2022). Discovery of coordinately regulated pathways that provide innate protection against interbacterial antagonism. eLife. 11. 11 indexed citations
6.
Morgan, Sarah J., Sumedha Ravishankar, Peter Jorth, et al.. (2021). A population-level strain genotyping method to study pathogen strain dynamics in human infections. JCI Insight. 6(24). 3 indexed citations
7.
Moraes, Marcos H. de, FoSheng Hsu, Dustin E. Bosch, et al.. (2021). An interbacterial DNA deaminase toxin directly mutagenizes surviving target populations. eLife. 10. 31 indexed citations
8.
Mok, Beverly, Marcos H. de Moraes, Jun Zeng, et al.. (2020). A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing. Nature. 583(7817). 631–637. 483 indexed citations breakdown →
9.
Radey, Matthew C., et al.. (2019). Escherichia coli Clonobiome: Assessing the Strain Diversity in Feces and Urine by Deep Amplicon Sequencing. Applied and Environmental Microbiology. 85(23). 8 indexed citations
10.
Nelson, Maria T., Christopher E. Pope, Robyn L. Marsh, et al.. (2019). Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles. Cell Reports. 26(8). 2227–2240.e5. 109 indexed citations
11.
Ross, Benjamin D., Beth M. Hayes, Matthew C. Radey, et al.. (2018). Ixodes scapularis does not harbor a stable midgut microbiome. The ISME Journal. 12(11). 2596–2607. 80 indexed citations
12.
Akullian, Adam, Joel M. Montgomery, Grace John‐Stewart, et al.. (2018). Multi-drug resistant non-typhoidal Salmonella associated with invasive disease in western Kenya. PLoS neglected tropical diseases. 12(1). e0006156–e0006156. 27 indexed citations
13.
Tchesnokova, Veronika, Elena Rechkina, Diana Chan, et al.. (2017). Bacterial clonal diagnostics as a tool for evidence-based empiric antibiotic selection. PLoS ONE. 12(3). e0174132–e0174132. 17 indexed citations
14.
Verster, Adrian J., Benjamin D. Ross, Matthew C. Radey, et al.. (2017). The Landscape of Type VI Secretion across Human Gut Microbiomes Reveals Its Role in Community Composition. Cell Host & Microbe. 22(3). 411–419.e4. 113 indexed citations
15.
Armbruster, Catherine R., Daniel J. Wolter, Meenu Mishra, et al.. (2016). Staphylococcus aureus Protein A Mediates Interspecies Interactions at the Cell Surface of Pseudomonas aeruginosa. mBio. 7(3). 83 indexed citations
16.
Brittnacher, M., Sonya L. Heltshe, Hillary S. Hayden, et al.. (2016). GUTSS: An Alignment-Free Sequence Comparison Method for Use in Human Intestinal Microbiome and Fecal Microbiota Transplantation Analysis. PLoS ONE. 11(7). e0158897–e0158897. 6 indexed citations
17.
Manor, Ohad, Roie Levy, Christopher E. Pope, et al.. (2016). Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosis. Scientific Reports. 6(1). 22493–22493. 97 indexed citations
18.
Damman, Christopher J., M. Brittnacher, Maria Westerhoff, et al.. (2015). Low Level Engraftment and Improvement following a Single Colonoscopic Administration of Fecal Microbiota to Patients with Ulcerative Colitis. PLoS ONE. 10(8). e0133925–e0133925. 57 indexed citations
19.
Rohmer, Laurence, Michael Jacobs, M. Brittnacher, et al.. (2014). Genomic analysis of the emergence of 20th century epidemic dysentery. BMC Genomics. 15(1). 355–355. 18 indexed citations
20.
Hayden, Hillary S., Regina Lim, M. Brittnacher, et al.. (2012). Evolution of Burkholderia pseudomallei in Recurrent Melioidosis. PLoS ONE. 7(5). e36507–e36507. 93 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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