Lars Jelsbak

12.4k total citations · 2 hit papers
77 papers, 5.3k citations indexed

About

Lars Jelsbak is a scholar working on Molecular Biology, Genetics and Molecular Medicine. According to data from OpenAlex, Lars Jelsbak has authored 77 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 26 papers in Genetics and 22 papers in Molecular Medicine. Recurrent topics in Lars Jelsbak's work include Bacterial biofilms and quorum sensing (33 papers), Bacterial Genetics and Biotechnology (23 papers) and Antibiotic Resistance in Bacteria (22 papers). Lars Jelsbak is often cited by papers focused on Bacterial biofilms and quorum sensing (33 papers), Bacterial Genetics and Biotechnology (23 papers) and Antibiotic Resistance in Bacteria (22 papers). Lars Jelsbak collaborates with scholars based in Denmark, United States and United Kingdom. Lars Jelsbak's co-authors include Søren Molin, Rasmus L. Marvig, Helle Krogh Johansen, Niels Høiby, Lei Yang, Ole Lund, Frank M. Aarestrup, Mette Voldby Larsen, Carsten Friis and Thomas Sicheritz‐Pontén and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Lars Jelsbak

74 papers receiving 5.3k citations

Hit Papers

Multilocus Sequence Typing of Total-Genome-Sequenced Bact... 2012 2026 2016 2021 2012 2012 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lars Jelsbak Denmark 31 2.9k 2.0k 1.2k 1.0k 943 77 5.3k
Rasmus L. Marvig Denmark 27 2.4k 0.8× 2.0k 1.0× 1.2k 1.0× 922 0.9× 700 0.7× 61 4.7k
Alan R. Hauser United States 47 4.5k 1.6× 3.3k 1.6× 2.0k 1.7× 1.3k 1.3× 759 0.8× 126 8.1k
José A. Bengoechea Spain 44 2.0k 0.7× 2.5k 1.2× 1.5k 1.2× 1.1k 1.1× 363 0.4× 111 6.3k
Matthew C. Wolfgang United States 46 4.5k 1.6× 1.3k 0.6× 1.4k 1.2× 2.1k 2.1× 1.6k 1.7× 91 7.0k
Vaughn S. Cooper United States 40 2.3k 0.8× 1.1k 0.6× 772 0.6× 2.0k 2.0× 278 0.3× 142 5.2k
Thomas Bruun Rasmussen Denmark 32 2.9k 1.0× 795 0.4× 542 0.4× 613 0.6× 305 0.3× 115 5.5k
Derek W. Hood United Kingdom 43 3.3k 1.2× 536 0.3× 996 0.8× 1.2k 1.2× 269 0.3× 126 6.6k
Lucía Fernández Spain 36 2.3k 0.8× 1.5k 0.7× 734 0.6× 730 0.7× 118 0.1× 104 5.0k
Sebastián Albertí Spain 44 1.7k 0.6× 4.1k 2.0× 1.9k 1.6× 651 0.6× 148 0.2× 97 6.4k
Vincent T. Lee United States 36 3.1k 1.1× 862 0.4× 1.1k 0.9× 1.7k 1.7× 139 0.1× 82 4.5k

Countries citing papers authored by Lars Jelsbak

Since Specialization
Citations

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

Fields of papers citing papers by Lars Jelsbak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lars Jelsbak

This figure shows the co-authorship network connecting the top 25 collaborators of Lars Jelsbak. A scholar is included among the top collaborators of Lars Jelsbak 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 Lars Jelsbak. Lars Jelsbak 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.
Bay, Lene, et al.. (2025). Evaluating antimicrobial efficacy in medical devices: The critical role of simulating in use test conditions. Biomaterials Advances. 172. 214241–214241. 1 indexed citations
2.
Jarmusch, Scott A., Mario Wibowo, Carlos N. Lozano-Andrade, et al.. (2024). Resistance towards and biotransformation of a Pseudomonas-produced secondary metabolite during community invasion. The ISME Journal. 18(1). 10 indexed citations
3.
Larsen, Inge, Julie Elvekjær Hansen, Anna Cäcilia Ingham, et al.. (2023). The effects of antibiotic use on the dynamics of the microbiome and resistome in pigs. SHILAP Revista de lepidopterología. 5(1). 39–39. 12 indexed citations
4.
Ghoul, Melanie, Sandra B. Andersen, Rasmus L. Marvig, et al.. (2023). Long-term evolution of antibiotic tolerance in Pseudomonas aeruginosa lung infections. Evolution Letters. 7(6). 389–400. 7 indexed citations
5.
Zhao, Yonggang, et al.. (2023). Whole-genome sequencing reveals high-risk clones of Pseudomonas aeruginosa in Guangdong, China. Frontiers in Microbiology. 14. 1117017–1117017. 18 indexed citations
6.
Zhao, Yonggang, et al.. (2023). Comparative whole-genome analysis of China and global epidemic Pseudomonas aeruginosa high-risk clones. Journal of Global Antimicrobial Resistance. 35. 149–158. 7 indexed citations
7.
Fiil, Berthe Katrine, Sandra Wingaard Thrane, Michael Jakob Pichler, et al.. (2022). Orally active bivalent VHH construct prevents proliferation of F4+ enterotoxigenic Escherichia coli in weaned piglets. iScience. 25(4). 104003–104003. 19 indexed citations
8.
Bech, Pernille Kjersgaard, et al.. (2021). Identification and Differentiation of Pseudomonas Species in Field Samples Using an rpoD Amplicon Sequencing Methodology. mSystems. 6(4). e0070421–e0070421. 19 indexed citations
9.
Filho, Rafael Antonio Casarin Penha, et al.. (2021). The plasmidome of multidrug-resistant emergent Salmonella serovars isolated from poultry. Infection Genetics and Evolution. 89. 104716–104716. 10 indexed citations
10.
Jelsbak, Lars, et al.. (2019). A Rare Thioquinolobactin Siderophore Present in a Bioactive Pseudomonas sp. DTU12.1. Genome Biology and Evolution. 11(12). 3529–3533. 6 indexed citations
11.
Boysen, Anders, et al.. (2018). HldE Is Important for Virulence Phenotypes in Enterotoxigenic Escherichia coli. Frontiers in Cellular and Infection Microbiology. 8. 253–253. 14 indexed citations
12.
Sommer, Lea M., Helle Krogh Johansen, Tomas Rindzevicius, et al.. (2017). SERS detection of the biomarker hydrogen cyanide from Pseudomonas aeruginosa cultures isolated from cystic fibrosis patients. Scientific Reports. 7(1). 45264–45264. 28 indexed citations
13.
Bartell, Jennifer, Anna S. Blazier, P. H. Yen, et al.. (2017). Reconstruction of the metabolic network of Pseudomonas aeruginosa to interrogate virulence factor synthesis. Nature Communications. 8(1). 14631–14631. 94 indexed citations
14.
Marvig, Rasmus L., et al.. (2016). The evolution of antimicrobial peptide resistance in Pseudomonas aeruginosa is shaped by strong epistatic interactions. Nature Communications. 7(1). 13002–13002. 105 indexed citations
15.
Taylor, Véronique L., et al.. (2016). A Bacteriophage-Acquired O-Antigen Polymerase (Wzyβ) from P. aeruginosa Serotype O16 Performs a Varied Mechanism Compared to Its Cognate Wzyα. Frontiers in Microbiology. 7. 393–393. 9 indexed citations
17.
Molin, Søren, et al.. (2012). Symposium Summaries. Pediatric Pulmonology. 47(S35). 108–222. 1 indexed citations
18.
Yang, Lei, Lars Jelsbak, Rasmus L. Marvig, et al.. (2011). Evolutionary dynamics of bacteria in a human host environment. Proceedings of the National Academy of Sciences. 108(18). 7481–7486. 267 indexed citations
19.
Yang, Lei, Martin Holm Rau, Liang Yang, et al.. (2011). Bacterial adaptation during chronic infection revealed by independent component analysis of transcriptomic data. BMC Microbiology. 11(1). 184–184. 19 indexed citations
20.
Jelsbak, Lars & Lotte Søgaard‐Andersen. (2003). Cell behavior and cell–cell communication during fruiting body morphogenesis in Myxococcus xanthus. Journal of Microbiological Methods. 55(3). 829–839. 40 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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