Nathalie Connil

1.6k total citations
33 papers, 1.2k citations indexed

About

Nathalie Connil is a scholar working on Molecular Biology, Food Science and Genetics. According to data from OpenAlex, Nathalie Connil has authored 33 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Food Science and 7 papers in Genetics. Recurrent topics in Nathalie Connil's work include Probiotics and Fermented Foods (17 papers), Gut microbiota and health (12 papers) and Bacterial biofilms and quorum sensing (8 papers). Nathalie Connil is often cited by papers focused on Probiotics and Fermented Foods (17 papers), Gut microbiota and health (12 papers) and Bacterial biofilms and quorum sensing (8 papers). Nathalie Connil collaborates with scholars based in France, Tunisia and Saudi Arabia. Nathalie Connil's co-authors include Marc Feuilloley, Mohamed Zommiti, Mounir Ferchichi, Hervé Prévost, Olivier Maillot, Xavier Dousset, Gilles Kergourlay, Mohamed Manaï, Jean‐Marc Chobert and Soumaya Messaoudi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Nathalie Connil

31 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathalie Connil France 18 734 603 210 128 125 33 1.2k
Birgitte Stuer‐Lauridsen Denmark 16 702 1.0× 643 1.1× 253 1.2× 83 0.6× 67 0.5× 19 1.1k
Yanath Belguesmia France 19 710 1.0× 901 1.5× 278 1.3× 108 0.8× 155 1.2× 51 1.4k
Jacques Frère France 22 641 0.9× 549 0.9× 159 0.8× 88 0.7× 77 0.6× 34 1.2k
Núria Piqué Spain 19 587 0.8× 359 0.6× 137 0.7× 82 0.6× 58 0.5× 44 1.4k
Toshihiro Sashihara Japan 22 825 1.1× 978 1.6× 342 1.6× 112 0.9× 164 1.3× 41 1.6k
Tung‐Ching Chung Taiwan 12 732 1.0× 873 1.4× 350 1.7× 120 0.9× 56 0.4× 21 1.3k
Tingting Guo China 19 564 0.8× 410 0.7× 126 0.6× 66 0.5× 51 0.4× 58 911
Kwang‐Young Song South Korea 19 642 0.9× 853 1.4× 246 1.2× 118 0.9× 34 0.3× 126 1.5k
Udo Wegmann United Kingdom 21 957 1.3× 649 1.1× 244 1.2× 167 1.3× 155 1.2× 37 1.4k
Do‐Won Jeong South Korea 21 975 1.3× 872 1.4× 182 0.9× 358 2.8× 100 0.8× 114 1.7k

Countries citing papers authored by Nathalie Connil

Since Specialization
Citations

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

Fields of papers citing papers by Nathalie Connil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Connil

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Connil. A scholar is included among the top collaborators of Nathalie Connil 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 Nathalie Connil. Nathalie Connil 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
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Boukerb, Amine M., et al.. (2024). Bacterial gene expression in response to catecholamine stress hormones. Current Opinion in Endocrine and Metabolic Research. 36. 100543–100543. 1 indexed citations
4.
Fijan, Sabina, et al.. (2023). Overview of Probiotic Strains of Weizmannia coagulans, Previously Known as Bacillus coagulans, as Food Supplements and Their Use in Human Health. SHILAP Revista de lepidopterología. 3(3). 935–947. 9 indexed citations
5.
Zommiti, Mohamed, Nathalie Connil, Ali Tahrioui, et al.. (2022). Organs-on-Chips Platforms Are Everywhere: A Zoom on Biomedical Investigation. Bioengineering. 9(11). 646–646. 22 indexed citations
6.
Ferchichi, Mounir, Khaled Sebei, Amine M. Boukerb, et al.. (2021). Enterococcus spp.: Is It a Bad Choice for a Good Use—A Conundrum to Solve?. Microorganisms. 9(11). 2222–2222. 31 indexed citations
7.
Boukerb, Amine M., Mélyssa Cambronel, Sophie Rodrigues, et al.. (2021). Inter-Kingdom Signaling of Stress Hormones: Sensing, Transport and Modulation of Bacterial Physiology. Frontiers in Microbiology. 12. 690942–690942. 27 indexed citations
8.
Zommiti, Mohamed, Mounir Ferchichi, Khaled Sebei, et al.. (2020). Draft Genome Sequences of Five Potentially Probiotic Enterococcus faecium Strains Isolated from an Artisanal Tunisian Meat (Dried Ossban). Microbiology Resource Announcements. 9(3). 4 indexed citations
9.
Cambronel, Mélyssa, Olivier Maillot, Laure Taupin, et al.. (2019). Epinephrine affects motility, and increases adhesion, biofilm and virulence of Pseudomonas aeruginosa H103. Scientific Reports. 9(1). 20203–20203. 38 indexed citations
10.
Zommiti, Mohamed, Emeline Bouffartigues, Olivier Maillot, et al.. (2018). In vitro Assessment of the Probiotic Properties and Bacteriocinogenic Potential of Pediococcus pentosaceus MZF16 Isolated From Artisanal Tunisian Meat “Dried Ossban”. Frontiers in Microbiology. 9. 2607–2607. 60 indexed citations
11.
Zommiti, Mohamed, Mélyssa Cambronel, Olivier Maillot, et al.. (2018). Evaluation of Probiotic Properties and Safety of Enterococcus faecium Isolated From Artisanal Tunisian Meat “Dried Ossban”. Frontiers in Microbiology. 9. 1685–1685. 100 indexed citations
12.
Szunerits, Sabine, Rabah Boukherroub, Awa Ndiaye, et al.. (2017). Substance P enhances lactic acid and tyramine production in Enterococcus faecalis V583 and promotes its cytotoxic effect on intestinal Caco-2/TC7 cells. Gut Pathogens. 9(1). 20–20. 12 indexed citations
13.
Nabhani, Ziad Al, Nicolas Montcuquet, Monique Dussaillant, et al.. (2015). Pseudomonas fluorescens Alters the Intestinal Barrier Function by Modulating IL-1β Expression Through Hematopoietic NOD2 Signaling. Inflammatory Bowel Diseases. 21(3). 543–555. 25 indexed citations
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Barbey, Corinne, et al.. (2015). The pathogenic potential of Pseudomonas fluorescens MFN1032 on enterocytes can be modulated by serotonin, substance P and epinephrine. Archives of Microbiology. 197(8). 983–990. 32 indexed citations
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Messaoudi, Soumaya, Mohamed Manaï, Gilles Kergourlay, et al.. (2013). Lactobacillus salivarius: Bacteriocin and probiotic activity. Food Microbiology. 36(2). 296–304. 193 indexed citations
16.
Bouffartigues, Emeline, Manjeet Bains, Virginie Oxaran, et al.. (2013). The Extra-Cytoplasmic Function Sigma Factor SigX Modulates Biofilm and Virulence-Related Properties in Pseudomonas aeruginosa. PLoS ONE. 8(11). e80407–e80407. 41 indexed citations
17.
Reffuveille, Fany, Nathalie Connil, Maurizio Sanguinetti, et al.. (2012). Involvement of Peptidylprolyl cis / trans Isomerases in Enterococcus faecalis Virulence. Infection and Immunity. 80(5). 1728–1735. 31 indexed citations
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Madi, Amar, et al.. (2010). Pseudomonas fluorescens alters epithelial permeability and translocates across Caco-2/TC7 intestinal cells. Gut Pathogens. 2(1). 16–16. 27 indexed citations
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Belguesmia, Yanath, Amar Madi, Annabelle Mérieau, et al.. (2010). Growing insights into the safety of bacteriocins: the case of enterocin S37. Research in Microbiology. 162(2). 159–163. 40 indexed citations
20.
Lesouhaitier, Olivier, Wilfried Véron, Annelise Chapalain, et al.. (2009). Gram-Negative Bacterial Sensors for Eukaryotic Signal Molecules. Sensors. 9(9). 6967–6990. 51 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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