Dorte Frees

4.8k total citations · 1 hit paper
69 papers, 3.5k citations indexed

About

Dorte Frees is a scholar working on Infectious Diseases, Molecular Biology and Genetics. According to data from OpenAlex, Dorte Frees has authored 69 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Infectious Diseases, 40 papers in Molecular Biology and 29 papers in Genetics. Recurrent topics in Dorte Frees's work include Antimicrobial Resistance in Staphylococcus (44 papers), Bacterial Genetics and Biotechnology (29 papers) and Bacterial biofilms and quorum sensing (27 papers). Dorte Frees is often cited by papers focused on Antimicrobial Resistance in Staphylococcus (44 papers), Bacterial Genetics and Biotechnology (29 papers) and Bacterial biofilms and quorum sensing (27 papers). Dorte Frees collaborates with scholars based in Denmark, United Kingdom and United States. Dorte Frees's co-authors include Hanne Ingmer, Martin Vestergaard, Philip J. Hill, Saara N. A. Qazi, Pekka Varmanen, Kirsi Savijoki, Karen Kristine Sørensen, Ulf Gerth, Kristoffer T. Bæk and Marianne Thorup Cohn and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Dorte Frees

67 papers receiving 3.5k citations

Hit Papers

Antibiotic Resistance and the MRSA Problem 2019 2026 2021 2023 2019 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorte Frees Denmark 34 2.2k 1.5k 736 487 440 69 3.5k
Greg A. Somerville United States 36 2.3k 1.1× 1.9k 1.3× 830 1.1× 389 0.8× 192 0.4× 57 3.6k
Lindsey N. Shaw United States 35 2.9k 1.3× 2.0k 1.3× 609 0.8× 871 1.8× 210 0.5× 124 4.5k
Ian R. Monk Australia 31 2.0k 0.9× 1.6k 1.0× 516 0.7× 298 0.6× 461 1.0× 78 3.5k
Christopher Weidenmaier Germany 33 2.6k 1.2× 2.0k 1.3× 445 0.6× 1.2k 2.4× 609 1.4× 50 4.8k
Bernhard Krismer Germany 25 1.9k 0.9× 1.1k 0.7× 341 0.5× 620 1.3× 528 1.2× 42 3.4k
Taeok Bae United States 34 3.4k 1.5× 2.9k 1.9× 1.1k 1.5× 687 1.4× 260 0.6× 73 4.9k
Jean-Christophe Giárd France 36 1.4k 0.6× 1.2k 0.8× 505 0.7× 207 0.4× 757 1.7× 88 3.3k
François Malouin Canada 40 1.9k 0.9× 1.2k 0.8× 494 0.7× 723 1.5× 986 2.2× 123 4.6k
Wilma Ziebuhr Germany 35 2.6k 1.2× 2.2k 1.5× 363 0.5× 516 1.1× 223 0.5× 77 4.0k
John F. Kokai‐Kun United States 27 1.6k 0.7× 1.8k 1.2× 269 0.4× 516 1.1× 292 0.7× 47 3.0k

Countries citing papers authored by Dorte Frees

Since Specialization
Citations

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

Fields of papers citing papers by Dorte Frees

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dorte Frees. 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 Dorte Frees. The network helps show where Dorte Frees may publish in the future.

Co-authorship network of co-authors of Dorte Frees

This figure shows the co-authorship network connecting the top 25 collaborators of Dorte Frees. A scholar is included among the top collaborators of Dorte Frees 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 Dorte Frees. Dorte Frees 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.
Borre, Michael, Martin S. Bojer, Danae Morales Angeles, et al.. (2025). Temperature-dependent regulation of bacterial cell division hydrolases by the coordinated action of a regulatory RNA and the ClpXP protease. PubMed. 13. 100144–100144. 1 indexed citations
2.
Salazar, Manuela Gesell, et al.. (2025). The ClpXP protease and the ClpX unfoldase control virulence, cell division, and autolysis in Streptococcus pneumoniae. Microbiology Spectrum. 13(7). e0080425–e0080425.
4.
Alqarzaee, Abdulelah A., Sujata S. Chaudhari, Mohammad Mazharul Islam, et al.. (2021). Staphylococcal ClpXP protease targets the cellular antioxidant system to eliminate fitness-compromised cells in stationary phase. Proceedings of the National Academy of Sciences. 118(47). 14 indexed citations
5.
Aldana, Blanca I., Romain Guérillot, Sofie Hedlund Møller, et al.. (2020). Staphylococcus aureus induces cell-surface expression of immune stimulatory NKG2D ligands on human monocytes. Journal of Biological Chemistry. 295(33). 11803–11821. 11 indexed citations
6.
Li, Heng, et al.. (2020). Nisin Damages the Septal Membrane and Triggers DNA Condensation in Methicillin-Resistant Staphylococcus aureus. Frontiers in Microbiology. 11. 1007–1007. 44 indexed citations
7.
Bojer, Martin S., Dorte Frees, & Hanne Ingmer. (2020). SosA in Staphylococci: an addition to the paradigm of membrane-localized, SOS-induced cell division inhibition in bacteria. Current Genetics. 66(3). 495–499. 9 indexed citations
8.
Schelin, Jenny, et al.. (2020). A Functional ClpXP Protease is Required for Induction of the Accessory Toxin Genes, tst, sed, and sec. Toxins. 12(9). 553–553. 7 indexed citations
9.
Bojer, Martin S., Clément Gallay, Amy L. Bottomley, et al.. (2019). SosA inhibits cell division in Staphylococcus aureus in response to DNA damage. Molecular Microbiology. 112(4). 1116–1130. 24 indexed citations
10.
Bæk, Kristoffer T., Clément Gallay, Lijuan Xu, et al.. (2019). The ClpX chaperone controls autolytic splitting of Staphylococcus aureus daughter cells, but is bypassed by β-lactam antibiotics or inhibitors of WTA biosynthesis. PLoS Pathogens. 15(9). e1008044–e1008044. 33 indexed citations
11.
Nielsen, Anita Kildebæk, Maria Månsson, Martin S. Bojer, et al.. (2014). Solonamide B Inhibits Quorum Sensing and Reduces Staphylococcus aureus Mediated Killing of Human Neutrophils. PLoS ONE. 9(1). e84992–e84992. 89 indexed citations
12.
Farrand, Allison J., Michelle L. Reniere, Hanne Ingmer, Dorte Frees, & Eric P. Skaar. (2013). Regulation of Host Hemoglobin Binding by the Staphylococcus aureus Clp Proteolytic System. Journal of Bacteriology. 195(22). 5041–5050. 42 indexed citations
13.
Jensen, Louise Kruse, Janne Koch, Klaus Kirketerp‐Møller, et al.. (2013). Therapy of haematogenous osteomyelitis--a comparative study in a porcine model and Angolan children.. PubMed. 27(3). 305–12. 13 indexed citations
14.
Haaber, Jakob, Marianne Thorup Cohn, Dorte Frees, Thorbjørn Joest Andersen, & Hanne Ingmer. (2012). Planktonic Aggregates of Staphylococcus aureus Protect against Common Antibiotics. PLoS ONE. 7(7). e41075–e41075. 147 indexed citations
15.
Rogstam, Annika, et al.. (2011). The YjbH Adaptor Protein Enhances Proteolysis of the Transcriptional Regulator Spx in Staphylococcus aureus. Journal of Bacteriology. 194(5). 1186–1194. 53 indexed citations
16.
Jensen, Louise Kruse, Dorte Frees, Bent Aalbæk, et al.. (2010). A porcine model of acute, haematogenous, localized osteomyelitis due to Staphylococcus aureus: a pathomorphological study. Apmis. 119(2). 111–118. 35 indexed citations
17.
Frees, Dorte, et al.. (2009). GtxA fromGallibacterium anatis, a cytolytic RTX-toxin with a novel domain organisation. Veterinary Research. 41(3). 25–25. 41 indexed citations
18.
Jelsbak, Lotte, Stefanie Donat, Knut Ohlsen, et al.. (2009). Growth phase-dependent regulation of the global virulence regulator Rot in clinical isolates of Staphylococcus aureus. International Journal of Medical Microbiology. 300(4). 229–236. 25 indexed citations
19.
Frees, Dorte, Line Elnif Thomsen, & Hanne Ingmer. (2005). Staphylococcus aureus ClpYQ plays a minor role in stress survival. Archives of Microbiology. 183(4). 286–291. 24 indexed citations
20.
Savijoki, Kirsi, Hanne Ingmer, Dorte Frees, et al.. (2003). Heat and DNA damage induction of the LexA‐like regulator HdiR from Lactococcus lactis is mediated by RecA and ClpP. Molecular Microbiology. 50(2). 609–621. 41 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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