Vanessa Khemici

1.1k total citations
17 papers, 712 citations indexed

About

Vanessa Khemici is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Vanessa Khemici has authored 17 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Ecology. Recurrent topics in Vanessa Khemici's work include Bacterial Genetics and Biotechnology (14 papers), RNA and protein synthesis mechanisms (14 papers) and Bacteriophages and microbial interactions (4 papers). Vanessa Khemici is often cited by papers focused on Bacterial Genetics and Biotechnology (14 papers), RNA and protein synthesis mechanisms (14 papers) and Bacteriophages and microbial interactions (4 papers). Vanessa Khemici collaborates with scholars based in France, Switzerland and United Kingdom. Vanessa Khemici's co-authors include Agamemnon J. Carpousis, Leonora Poljak, Patrick Linder, Ben F. Luisi, Isabelle Toesca, Peter Redder, Nathalie Vanzo, Julien Prados, Stéphane Hausmann and Patrice Polard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Methods in enzymology on CD-ROM/Methods in enzymology and Molecular Microbiology.

In The Last Decade

Vanessa Khemici

17 papers receiving 707 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vanessa Khemici France 12 620 437 225 43 40 17 712
Mark Chlenov United States 6 694 1.1× 484 1.1× 241 1.1× 27 0.6× 58 1.4× 6 776
Nelly Said Germany 11 825 1.3× 557 1.3× 386 1.7× 40 0.9× 28 0.7× 18 954
Yuri A. Nedialkov United States 17 874 1.4× 450 1.0× 100 0.4× 35 0.8× 38 0.9× 26 1.0k
Peggy Mervelet France 7 420 0.7× 297 0.7× 147 0.7× 28 0.7× 61 1.5× 7 533
Isabelle Iost France 15 1.4k 2.2× 591 1.4× 287 1.3× 56 1.3× 34 0.8× 20 1.5k
Akira Ishihama Japan 8 566 0.9× 456 1.0× 198 0.9× 34 0.8× 50 1.3× 9 681
Albertas Timinskas Lithuania 16 598 1.0× 250 0.6× 184 0.8× 70 1.6× 44 1.1× 23 761
Yvonne Göpel Austria 13 391 0.6× 330 0.8× 176 0.8× 36 0.8× 49 1.2× 15 544
Sandro Zangrossi Italy 16 522 0.8× 378 0.9× 272 1.2× 26 0.6× 41 1.0× 19 610
Christopher D. A. Rodrigues United States 15 467 0.8× 388 0.9× 284 1.3× 85 2.0× 53 1.3× 29 692

Countries citing papers authored by Vanessa Khemici

Since Specialization
Citations

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

Fields of papers citing papers by Vanessa Khemici

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vanessa Khemici

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

All Works

17 of 17 papers shown
1.
Khemici, Vanessa, Stéphane Hausmann, Julien Prados, et al.. (2021). RNase J1 and J2 Are Host-Encoded Factors for Plasmid Replication. Frontiers in Microbiology. 12. 586886–586886. 3 indexed citations
2.
Khemici, Vanessa, Marc Prudhomme, & Patrice Polard. (2021). Tight Interplay between Replication Stress and Competence Induction in Streptococcus pneumoniae. Cells. 10(8). 1938–1938. 9 indexed citations
3.
Khemici, Vanessa, et al.. (2020). The DEAD-box RNA helicase CshA is required for fatty acid homeostasis in Staphylococcus aureus. PLoS Genetics. 16(7). e1008779–e1008779. 4 indexed citations
4.
Johnston, Calum, et al.. (2018). Fine‐tuning cellular levels of DprA ensures transformant fitness in the human pathogen Streptococcus pneumoniae. Molecular Microbiology. 109(5). 663–675. 17 indexed citations
5.
Khemici, Vanessa & Patrick Linder. (2018). RNA helicases in RNA decay. Biochemical Society Transactions. 46(1). 163–172. 20 indexed citations
6.
Khemici, Vanessa & Patrick Linder. (2016). RNA helicases in bacteria. Current Opinion in Microbiology. 30. 58–66. 21 indexed citations
7.
Redder, Peter, et al.. (2015). Bacterial versatility requires DEAD-box RNA helicases. FEMS Microbiology Reviews. 39(3). 392–412. 62 indexed citations
8.
Khemici, Vanessa, Julien Prados, Patrick Linder, & Peter Redder. (2015). Decay-Initiating Endoribonucleolytic Cleavage by RNase Y Is Kept under Tight Control via Sequence Preference and Sub-cellular Localisation. PLoS Genetics. 11(10). e1005577–e1005577. 69 indexed citations
9.
Carpousis, Agamemnon J., Vanessa Khemici, & Leonora Poljak. (2008). Chapter 10 Assaying DEAD‐box RNA Helicases and Their Role in mRNA Degradation in Escherichia coli. Methods in enzymology on CD-ROM/Methods in enzymology. 447. 183–197. 5 indexed citations
10.
Carpousis, Agamemnon J., et al.. (2008). Chapter 4 Co‐immunopurification of Multiprotein Complexes Containing RNA‐Degrading Enzymes. Methods in enzymology on CD-ROM/Methods in enzymology. 447. 65–82. 13 indexed citations
11.
Khemici, Vanessa, Leonora Poljak, Ben F. Luisi, & Agamemnon J. Carpousis. (2008). The RNase E of Escherichia coli is a membrane‐binding protein. Molecular Microbiology. 70(4). 799–813. 160 indexed citations
12.
Yu, Jae‐Sung, Robert J. Kokoska, Vanessa Khemici, & Deborah A. Steege. (2006). In‐frame overlapping genes: the challenges for regulating gene expression. Molecular Microbiology. 63(4). 1158–1172. 8 indexed citations
13.
Khemici, Vanessa, Leonora Poljak, Isabelle Toesca, & Agamemnon J. Carpousis. (2005). Evidencein vivothat the DEAD-box RNA helicase RhlB facilitates the degradation of ribosome-free mRNA by RNase E. Proceedings of the National Academy of Sciences. 102(19). 6913–6918. 56 indexed citations
14.
Khemici, Vanessa, Isabelle Toesca, Leonora Poljak, Nathalie Vanzo, & Agamemnon J. Carpousis. (2004). The RNase E of Escherichia coli has at least two binding sites for DEAD‐box RNA helicases: functional replacement of RhlB by RhlE. Molecular Microbiology. 54(5). 1422–1430. 91 indexed citations
15.
Crozatier, Michèle, Bruno Glise, Vanessa Khemici, & Alain Vincent. (2003). Vein-positioning in the Drosophila wing in response to Hh; new roles of Notch signaling. Mechanisms of Development. 120(5). 529–535. 16 indexed citations
16.
Khemici, Vanessa & Agamemnon J. Carpousis. (2003). The RNA degradosome and poly(A) polymerase of Escherichia coli are required in vivo for the degradation of small mRNA decay intermediates containing REP‐stabilizers. Molecular Microbiology. 51(3). 777–790. 129 indexed citations
17.
Carpousis, Agamemnon J., et al.. (2001). Escherichia coli RNA Degradosome. Methods in enzymology on CD-ROM/Methods in enzymology. 342. 333–345. 29 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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