Stéphane Bach

3.2k total citations
97 papers, 2.2k citations indexed

About

Stéphane Bach is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Stéphane Bach has authored 97 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 46 papers in Organic Chemistry and 17 papers in Oncology. Recurrent topics in Stéphane Bach's work include Synthesis and biological activity (17 papers), Quinazolinone synthesis and applications (14 papers) and Cancer-related Molecular Pathways (12 papers). Stéphane Bach is often cited by papers focused on Synthesis and biological activity (17 papers), Quinazolinone synthesis and applications (14 papers) and Cancer-related Molecular Pathways (12 papers). Stéphane Bach collaborates with scholars based in France, South Africa and United States. Stéphane Bach's co-authors include Marc Blondel, Laurent Meijer, Hervé Galons, Sandrine Ruchaud, Caroline Corbel, Cyril Couturier, Déborah Tribouillard‐Tanvier, Blandine Baratte, Ralf Jockers and Nicolas Talarek and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Stéphane Bach

93 papers receiving 2.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Stéphane Bach 1.2k 585 263 229 172 97 2.2k
Mario A. Pagano 1.9k 1.5× 316 0.5× 368 1.4× 311 1.4× 118 0.7× 70 2.8k
Laurent Désaubry 1.8k 1.5× 611 1.0× 419 1.6× 212 0.9× 141 0.8× 90 3.2k
Hongyu Zhao 1.1k 0.9× 704 1.2× 153 0.6× 99 0.4× 142 0.8× 70 2.1k
Roberto Battistutta 2.1k 1.7× 414 0.7× 369 1.4× 178 0.8× 110 0.6× 69 3.1k
Victoria Magrioti 1.1k 0.9× 301 0.5× 89 0.3× 211 0.9× 239 1.4× 42 1.9k
Peter Chase 1.2k 1.0× 224 0.4× 221 0.8× 280 1.2× 62 0.4× 68 2.0k
Heather Hoover 1.5k 1.2× 361 0.6× 381 1.4× 333 1.5× 460 2.7× 17 2.3k
Balasundaram Padmanabhan 2.1k 1.7× 268 0.5× 190 0.7× 142 0.6× 61 0.4× 67 2.5k
J. Jefferson P. Perry 2.5k 2.0× 243 0.4× 680 2.6× 212 0.9× 92 0.5× 54 3.3k

Countries citing papers authored by Stéphane Bach

Since Specialization
Citations

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

Fields of papers citing papers by Stéphane Bach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphane Bach

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphane Bach. A scholar is included among the top collaborators of Stéphane Bach 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 Stéphane Bach. Stéphane Bach 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
3.
Bach, Stéphane, et al.. (2023). Overexpression of Eimeria tenella Rhoptry Kinase 2 Induces Early Production of Schizonts. Microbiology Spectrum. 11(4). e0013723–e0013723. 6 indexed citations
4.
Guillou, Catherine, Peter G. Goekjian, Pierre Garcia, et al.. (2022). An Optimized Workflow for the Discovery of New Antimicrobial Compounds Targeting Bacterial RNA Polymerase Complex Formation. Antibiotics. 11(10). 1449–1449. 4 indexed citations
5.
Guével, Rémy Le, Blandine Baratte, Thomas Robert, et al.. (2022). Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases. Molecules. 27(19). 6149–6149.
6.
Erb, William, Olivier Mongin, Nicolas Richy, et al.. (2021). Thiazolo[5,4‐f]quinoxalines, Oxazolo[5,4‐f]quinoxalines and Pyrazino[b,e]isatins: Synthesis from 6‐Aminoquinoxalines and Properties. European Journal of Organic Chemistry. 2021(19). 2756–2763. 4 indexed citations
7.
Ourliac‐Garnier, Isabelle, Cédric Logé, Florence O. McCarthy, et al.. (2021). Dibenzofuran Derivatives Inspired from Cercosporamide as Dual Inhibitors of Pim and CLK1 Kinases. Molecules. 26(21). 6572–6572. 3 indexed citations
8.
Legoabe, Lesetja J., et al.. (2020). Synthesis and biological evaluation of selected 7-azaindole derivatives as CDK9/Cyclin T and Haspin inhibitors. Medicinal Chemistry Research. 29(8). 1449–1462. 7 indexed citations
9.
Legoabe, Lesetja J., et al.. (2020). Synthesis and evaluation of C3 substituted chalcone‐based derivatives of 7‐azaindole as protein kinase inhibitors. Chemical Biology & Drug Design. 96(6). 1395–1407. 7 indexed citations
10.
Arzur, Danielle, Blandine Baratte, Thomas Robert, et al.. (2020). Regorafenib analogues and their ferrocenic counterparts: synthesis and biological evaluation. New Journal of Chemistry. 44(45). 19723–19733. 6 indexed citations
11.
Legoabe, Lesetja J., et al.. (2020). Synthesis and evaluation of 7-azaindole derivatives bearing benzocycloalkanone motifs as protein kinase inhibitors. Bioorganic & Medicinal Chemistry. 28(11). 115468–115468. 9 indexed citations
12.
Ibrahim, Nada, Pascal Bonnet, Jean‐Daniel Brion, et al.. (2020). Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency. European Journal of Medicinal Chemistry. 199. 112355–112355. 20 indexed citations
13.
Benchekroun, Mohamed, Ludmila Ermolenko, Blandine Baratte, et al.. (2020). Discovery of simplified benzazole fragments derived from the marine benzosceptrin B as necroptosis inhibitors involving the receptor interacting protein Kinase-1. European Journal of Medicinal Chemistry. 201. 112337–112337. 12 indexed citations
14.
Roca, Carlos, Concepción Pérez, Ana Martı́nez, et al.. (2019). From simple quinoxalines to potent oxazolo[5,4-f]quinoxaline inhibitors of glycogen-synthase kinase 3 (GSK3). Organic & Biomolecular Chemistry. 18(1). 154–162. 11 indexed citations
15.
Boukabcha, Nourdine, Necmi Dege, Sandrine Ruchaud, et al.. (2019). Synthesis and evaluation of new isatin-aminorhodanine hybrids as PIM1 and CLK1 kinase inhibitors. Journal of Molecular Structure. 1192. 82–90. 17 indexed citations
16.
Spadoni, Gilberto, Stéphane Bach, Monica Benincasa, et al.. (2019). New Antimicrobials Targeting Bacterial RNA Polymerase Holoenzyme Assembly Identified with an in Vivo BRET-Based Discovery Platform. ACS Chemical Biology. 14(8). 1727–1736. 10 indexed citations
17.
Masłyk, Maciej, Monika Janeczko, Małgorzata Tokarska-Rodak, et al.. (2019). The Anti-Candida albicans Agent 4-AN Inhibits Multiple Protein Kinases. Molecules. 24(1). 153–153. 6 indexed citations
18.
Oukoloff, Killian, Nicolas Coquelle, Manuela Bartolini, et al.. (2019). Design, biological evaluation and X-ray crystallography of nanomolar multifunctional ligands targeting simultaneously acetylcholinesterase and glycogen synthase kinase-3. European Journal of Medicinal Chemistry. 168. 58–77. 56 indexed citations
19.
Jégou, Camille, Arnaud Bondon, Stéphane Bach, et al.. (2017). Bioactive Metabolites from the Deep Subseafloor Fungus Oidiodendron griseum UBOCC-A-114129. Marine Drugs. 15(4). 111–111. 12 indexed citations
20.
Zhang, Bing, Caroline Corbel, Françoise Guéritte, et al.. (2011). An in silico approach for the discovery of CDK5/p25 interaction inhibitors. Biotechnology Journal. 6(7). 871–881. 17 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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