Dusko Ehrlich

1.9k total citations
19 papers, 1.5k citations indexed

About

Dusko Ehrlich is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Dusko Ehrlich has authored 19 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Ecology. Recurrent topics in Dusko Ehrlich's work include Bacterial Genetics and Biotechnology (7 papers), Bacteriophages and microbial interactions (5 papers) and Gut microbiota and health (5 papers). Dusko Ehrlich is often cited by papers focused on Bacterial Genetics and Biotechnology (7 papers), Bacteriophages and microbial interactions (5 papers) and Gut microbiota and health (5 papers). Dusko Ehrlich collaborates with scholars based in France, Morocco and United Kingdom. Dusko Ehrlich's co-authors include Emmanuelle Maguin, Alexandra Gruss, Patrick Duwat, Marie‐Christine Chopin, Stanislas Mondot, Marie Joossens, Jeroen Raes, Joël Doré, Marion Leclerc and Hervé M. Blottière and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Biotechnology and Gut.

In The Last Decade

Dusko Ehrlich

19 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dusko Ehrlich France 14 931 462 401 280 219 19 1.5k
Buffy Stahl United States 18 1.4k 1.5× 569 1.2× 435 1.1× 352 1.3× 160 0.7× 23 1.8k
Nityananda Chowdhury United States 25 650 0.7× 366 0.8× 290 0.7× 292 1.0× 152 0.7× 45 1.9k
Elżbieta Katarzyna Jagusztyn-Krynicka Poland 23 570 0.6× 578 1.3× 221 0.6× 188 0.7× 384 1.8× 79 1.6k
Ulla Svensson Sweden 23 755 0.8× 476 1.0× 425 1.1× 129 0.5× 177 0.8× 41 1.8k
Éric Guédon France 31 1.5k 1.6× 991 2.1× 444 1.1× 263 0.9× 245 1.1× 63 2.3k
Calum J. Walsh Ireland 18 1.1k 1.1× 498 1.1× 146 0.4× 200 0.7× 173 0.8× 36 1.6k
Udo Wegmann United Kingdom 21 957 1.0× 649 1.4× 197 0.5× 285 1.0× 167 0.8× 37 1.4k
Christine Delorme France 25 1.6k 1.7× 1.1k 2.4× 463 1.2× 254 0.9× 196 0.9× 48 2.2k
Cristiano G. Moreira Brazil 18 1.0k 1.1× 506 1.1× 391 1.0× 170 0.6× 482 2.2× 35 2.0k
Dusko S. Ehrlich France 9 790 0.8× 325 0.7× 160 0.4× 129 0.5× 149 0.7× 10 1.0k

Countries citing papers authored by Dusko Ehrlich

Since Specialization
Citations

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

Fields of papers citing papers by Dusko Ehrlich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dusko Ehrlich

This figure shows the co-authorship network connecting the top 25 collaborators of Dusko Ehrlich. A scholar is included among the top collaborators of Dusko Ehrlich 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 Dusko Ehrlich. Dusko Ehrlich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Berland, Magali, Florence Levenez, Nathalie Galleron, et al.. (2021). High engraftment capacity of frozen ready-to-use human fecal microbiota transplants assessed in germ-free mice. Scientific Reports. 11(1). 4365–4365. 8 indexed citations
2.
Ramayo‐Caldas, Yuliaxis, Laura M. Zingaretti, Milka Popova, et al.. (2019). Identification of rumen microbial biomarkers linked to methane emission in Holstein dairy cows. Journal of Animal Breeding and Genetics. 137(1). 49–59. 66 indexed citations
3.
4.
Solé, Cristina, Marta Llopis, Elsa Solà, et al.. (2018). Gut microbiome is profoundly altered in acute-on-chronic liver failure as evaluated by quantitative metagenomics. Relationship with liver cirrhosis severity. Journal of Hepatology. 68. S11–S12. 3 indexed citations
5.
Pavlidis, Polychronis, Nick Powell, Royce P Vincent, et al.. (2015). Systematic review: bile acids and intestinal inflammation‐luminal aggressors or regulators of mucosal defence?. Alimentary Pharmacology & Therapeutics. 42(7). 802–817. 106 indexed citations
6.
Nielsen, Henrik Bjørn, Mathieu Almeida, Agnieszka Sierakowska Juncker, et al.. (2014). A method for identifying metagenomic species and variable genetic elements by exhaustive co-abundance binning. Nature Biotechnology. 1 indexed citations
7.
Lepage, Patricia, Marion Leclerc, Marie Joossens, et al.. (2012). A metagenomic insight into our gut's microbiome. Gut. 62(1). 146–158. 268 indexed citations
8.
Loux, Valentin, Pierre Nicolas, Philippe Langella, et al.. (2008). Prediction of surface exposed proteins in Streptococcus pyogenes , with a potential application to other Gram‐positive bacteria. PROTEOMICS. 9(1). 61–73. 96 indexed citations
9.
Fernandez, Annabelle, Jun Ogawa, Stéphanie Penaud, et al.. (2008). Rerouting of pyruvate metabolism during acid adaptation in Lactobacillus bulgaricus. PROTEOMICS. 8(15). 3154–3163. 72 indexed citations
10.
Budin‐Verneuil, Aurélie, Vianney Pichereau, Yanick Auffray, Dusko Ehrlich, & Emmanuelle Maguin. (2007). Proteome phenotyping of acid stress‐resistant mutants of Lactococcus lactis MG1363. PROTEOMICS. 7(12). 2038–2046. 27 indexed citations
11.
Minić, Zoran, Corinne Marie, Christine Delorme, et al.. (2007). Control of EpsE, the Phosphoglycosyltransferase Initiating Exopolysaccharide Synthesis inStreptococcus thermophilus, by EpsD Tyrosine Kinase. Journal of Bacteriology. 189(4). 1351–1357. 77 indexed citations
12.
Petranović, Dina, et al.. (2004). Intracellular effectors regulating the activity of the Lactococcus lactis CodY pleiotropic transcription regulator. Molecular Microbiology. 53(2). 613–621. 82 indexed citations
13.
Grompone, Gianfranco, Dusko Ehrlich, & Bénédicte Michel. (2004). Cells defective for replication restart undergo replication fork reversal. EMBO Reports. 5(6). 607–612. 26 indexed citations
14.
Crispie, Fiona, et al.. (2002). Identification of a phosphofructokinase-encoding gene from Streptococcus thermophilus CNRZ1205 – a novel link between carbon metabolism and gene regulation?. Molecular Genetics and Genomics. 268(4). 500–509. 4 indexed citations
15.
Karoui, Meriem El, Dusko Ehrlich, & Alexandra Gruss. (1998). Identification of the lactococcal exonuclease/recombinase and its modulation by the putative Chi sequence. Proceedings of the National Academy of Sciences. 95(2). 626–631. 48 indexed citations
16.
Petit, Marie‐Agnès, Dusko Ehrlich, & Laurent Jannière. (1995). pAMβ1 resolvase has an atypical recombination site and requires a histone‐like protein HU. Molecular Microbiology. 18(2). 271–282. 57 indexed citations
17.
Hillier, Alan J., et al.. (1995). Characterization of the lactococcal abiD1 gene coding for phage abortive infection. Journal of Bacteriology. 177(13). 3818–3823. 73 indexed citations
18.
Ehrlich, Dusko, et al.. (1995). Phage operon involved in sensitivity to the Lactococcus lactis abortive infection mechanism AbiD1. Journal of Bacteriology. 177(13). 3824–3829. 71 indexed citations
19.
Maguin, Emmanuelle, et al.. (1992). New thermosensitive plasmid for gram-positive bacteria. Journal of Bacteriology. 174(17). 5633–5638. 365 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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