Christophe Corre

2.8k total citations
44 papers, 1.7k citations indexed

About

Christophe Corre is a scholar working on Pharmacology, Molecular Biology and Biotechnology. According to data from OpenAlex, Christophe Corre has authored 44 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Pharmacology, 28 papers in Molecular Biology and 10 papers in Biotechnology. Recurrent topics in Christophe Corre's work include Microbial Natural Products and Biosynthesis (32 papers), Plant biochemistry and biosynthesis (8 papers) and Genomics and Phylogenetic Studies (8 papers). Christophe Corre is often cited by papers focused on Microbial Natural Products and Biosynthesis (32 papers), Plant biochemistry and biosynthesis (8 papers) and Genomics and Phylogenetic Studies (8 papers). Christophe Corre collaborates with scholars based in United Kingdom, United States and France. Christophe Corre's co-authors include Gregory L. Challis, Lijiang Song, Bertrand Aigle, Pierre Leblond, Luisa Laureti, Fabrizio Alberti, Sheng Huang, Keith Chater, Sean O’Rourke and Stuart W. Haynes and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Christophe Corre

42 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christophe Corre United Kingdom 23 1.2k 1.1k 528 324 161 44 1.7k
Silke C. Wenzel Germany 33 1.5k 1.2× 1.6k 1.5× 671 1.3× 467 1.4× 190 1.2× 44 2.5k
Yiguang Zhu China 27 1.3k 1.1× 1.0k 1.0× 647 1.2× 657 2.0× 174 1.1× 96 2.0k
Mikko Metsä‐Ketelä Finland 25 1.2k 1.0× 1.1k 1.0× 430 0.8× 414 1.3× 177 1.1× 72 1.8k
Hongbo Huang China 28 1.7k 1.4× 1.1k 1.0× 889 1.7× 609 1.9× 194 1.2× 82 2.3k
Miho Izumikawa Japan 28 1.6k 1.3× 1.5k 1.4× 601 1.1× 614 1.9× 215 1.3× 87 2.4k
Zixin Deng China 24 807 0.7× 1.0k 0.9× 235 0.4× 343 1.1× 112 0.7× 84 1.5k
Patrick Rabe Germany 29 1.5k 1.3× 1.9k 1.7× 271 0.5× 281 0.9× 88 0.5× 59 2.4k
Alberto Plaza Italy 28 839 0.7× 1.3k 1.2× 499 0.9× 423 1.3× 256 1.6× 57 2.3k
Sumei Li China 24 885 0.7× 696 0.6× 496 0.9× 524 1.6× 171 1.1× 53 1.6k
Keishi Ishida Germany 27 1.3k 1.1× 1.2k 1.1× 416 0.8× 373 1.2× 276 1.7× 48 1.9k

Countries citing papers authored by Christophe Corre

Since Specialization
Citations

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

Fields of papers citing papers by Christophe Corre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christophe Corre

This figure shows the co-authorship network connecting the top 25 collaborators of Christophe Corre. A scholar is included among the top collaborators of Christophe Corre 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 Christophe Corre. Christophe Corre 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.
2.
Woolley, Jack M., et al.. (2023). Spectroscopic insight on impact of environment on natural photoprotectants. Chemical Science. 14(24). 6763–6769. 1 indexed citations
3.
Corre, Christophe, et al.. (2022). gcFront: a tool for determining a Pareto front of growth-coupled cell factory designs. Bioinformatics. 38(14). 3657–3659. 8 indexed citations
4.
Waschulin, Valentin, Chiara Borsetto, Robert James, et al.. (2021). Biosynthetic potential of uncultured Antarctic soil bacteria revealed through long-read metagenomic sequencing. The ISME Journal. 16(1). 101–111. 81 indexed citations
5.
Moore, Simon J., et al.. (2021). A Streptomyces venezuelae Cell-Free Toolkit for Synthetic Biology. ACS Synthetic Biology. 10(2). 402–411. 39 indexed citations
6.
Turner, Matthew A. P., et al.. (2021). Exploring the Blueprint of Photoprotection in Mycosporine-like Amino Acids. The Journal of Physical Chemistry Letters. 12(14). 3641–3646. 16 indexed citations
7.
Harrison, Peter J., Dean Rea, Matthew J. Belousoff, et al.. (2021). Molecular basis for control of antibiotic production by a bacterial hormone. Nature. 590(7846). 463–467. 21 indexed citations
8.
Sousoni, Despoina, et al.. (2020). Phytoplankton trigger the production of cryptic metabolites in the marine actinobacterium Salinispora tropica. Microbial Biotechnology. 14(1). 291–306. 15 indexed citations
9.
Song, Lijiang, et al.. (2020). MmfL catalyses formation of a phosphorylated butenolide intermediate in methylenomycin furan biosynthesis. Chemical Communications. 56(92). 14443–14446. 5 indexed citations
10.
Anonye, Blessing O., Ricky Cain, John Moat, et al.. (2020). Anti-biofilm efficacy of a medieval treatment for bacterial infection requires the combination of multiple ingredients. Scientific Reports. 10(1). 12687–12687. 23 indexed citations
11.
Alberti, Fabrizio, et al.. (2018). Triggering the expression of a silent gene cluster from genetically intractable bacteria results in scleric acid discovery. Chemical Science. 10(2). 453–463. 38 indexed citations
12.
Li, Xiao, et al.. (2017). Evidence for the formation of ScbR/ScbR2 heterodimers and identification of one of the regulatory targets in Streptomyces coelicolor. Applied Microbiology and Biotechnology. 101(13). 5333–5340. 3 indexed citations
13.
Song, Lijiang, Luisa Laureti, Christophe Corre, et al.. (2013). Cytochrome P450-mediated hydroxylation is required for polyketide macrolactonization in stambomycin biosynthesis. The Journal of Antibiotics. 67(1). 71–76. 22 indexed citations
14.
Corre, Christophe, et al.. (2012). Gamma-Butyrolactone and Furan Signaling Systems in Streptomyces. Methods in enzymology on CD-ROM/Methods in enzymology. 517. 71–87. 26 indexed citations
15.
Sydor, Paulina K., Sarah M. Barry, Francisco Barona‐Gómez, et al.. (2011). Regio- and stereodivergent antibiotic oxidative carbocyclizations catalysed by Rieske oxygenase-like enzymes. Nature Chemistry. 3(5). 388–392. 99 indexed citations
16.
Corre, Christophe, et al.. (2010). A butenolide intermediate in methylenomycin furan biosynthesis is implied by incorporation of stereospecifically 13C-labelled glycerols. Chemical Communications. 46(23). 4079–4079. 12 indexed citations
17.
Mo, SangJoon, Paulina K. Sydor, Christophe Corre, et al.. (2008). Elucidation of the Streptomyces coelicolor Pathway to 2-Undecylpyrrole, a Key Intermediate in Undecylprodiginine and Streptorubin B Biosynthesis. Chemistry & Biology. 15(2). 137–148. 78 indexed citations
18.
Corre, Christophe, et al.. (2006). Elucidation of the Streptomyces coelicolor pathway to 4-methoxy-2,2′-bipyrrole-5-carboxaldehyde, an intermediate in prodiginine biosynthesis. Chemical Communications. 3981–3983. 46 indexed citations
19.
Corre, Christophe & Gregory L. Challis. (2005). Evidence for the Unusual Condensation of a Diketide with a Pentulose in the Methylenomycin Biosynthetic Pathway of Streptomyces coelicolor A3(2). ChemBioChem. 6(12). 2166–2170. 26 indexed citations
20.
Corre, Christophe, et al.. (2004). Biosynthetic studies on the azinomycins: The pathway to the naphthoate fragment. Chemical Communications. 2600–2600. 13 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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