Éric Record

7.7k total citations
114 papers, 3.9k citations indexed

About

Éric Record is a scholar working on Plant Science, Biotechnology and Molecular Biology. According to data from OpenAlex, Éric Record has authored 114 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Plant Science, 56 papers in Biotechnology and 49 papers in Molecular Biology. Recurrent topics in Éric Record's work include Enzyme-mediated dye degradation (51 papers), Biofuel production and bioconversion (33 papers) and Microbial Metabolism and Applications (24 papers). Éric Record is often cited by papers focused on Enzyme-mediated dye degradation (51 papers), Biofuel production and bioconversion (33 papers) and Microbial Metabolism and Applications (24 papers). Éric Record collaborates with scholars based in France, Morocco and Tunisia. Éric Record's co-authors include Anthony Levasseur, Anne Lomascolo, Marcel Asther, Jean‐Claude Sigoillot, Marcel Asther, Jean‐Guy Berrin, Michèle Asther, Yonathan Arfi, David Navarro and Bernard Henrissat and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Environmental Science & Technology.

In The Last Decade

Éric Record

111 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Éric Record France 39 2.0k 1.7k 1.5k 1.4k 421 114 3.9k
Stephanie G. Burton South Africa 34 1.2k 0.6× 674 0.4× 1.5k 1.0× 615 0.4× 133 0.3× 111 3.6k
Heng Yin China 41 2.1k 1.0× 690 0.4× 1.5k 1.0× 548 0.4× 118 0.3× 178 5.0k
Rajinder K. Gupta India 30 1.2k 0.6× 429 0.3× 1.9k 1.3× 416 0.3× 430 1.0× 135 3.8k
Štefan Bauer United States 34 2.0k 1.0× 563 0.3× 1.7k 1.2× 1.7k 1.2× 93 0.2× 56 3.9k
Mirjam A. Kabel Netherlands 38 1.9k 1.0× 1.2k 0.7× 1.4k 1.0× 3.0k 2.1× 302 0.7× 136 4.8k
Chuan‐Chao Dai China 41 3.2k 1.6× 238 0.1× 1.3k 0.9× 297 0.2× 852 2.0× 208 5.0k
Harald Claus Germany 19 1.0k 0.5× 609 0.4× 626 0.4× 152 0.1× 122 0.3× 30 2.0k
Antonius J. A. van Maris Netherlands 45 803 0.4× 650 0.4× 5.6k 3.8× 3.3k 2.4× 197 0.5× 106 7.0k
Albert Krastanov Bulgaria 29 1.2k 0.6× 442 0.3× 988 0.7× 436 0.3× 169 0.4× 123 3.8k
Xuetong Fan United States 46 3.6k 1.8× 2.3k 1.3× 806 0.6× 463 0.3× 114 0.3× 241 7.2k

Countries citing papers authored by Éric Record

Since Specialization
Citations

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

Fields of papers citing papers by Éric Record

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Éric Record

This figure shows the co-authorship network connecting the top 25 collaborators of Éric Record. A scholar is included among the top collaborators of Éric Record 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 Éric Record. Éric Record 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.
Ezzariai, Amine, Jean Armengaud, Julien Lambert, et al.. (2025). Bjerkandera adusta TM11 for the bioremediation of fluoroquinolone antibiotics spiked in wastewater: A sustainable approach to pharmaceutical contaminant biotransformation. Ecotoxicology and Environmental Safety. 291. 117898–117898. 6 indexed citations
2.
Record, Éric, et al.. (2025). Optimization, characterization, and DFT study of activated-biochar from lignocellulosic biomass for fluoroquinolone antibiotic adsorption. Results in Engineering. 27. 106540–106540. 5 indexed citations
3.
Armengaud, Jean, David Navarro, Annick Turbé-Doan, et al.. (2025). Investigation into the potential of Bjerkandera adusta to biotransform the recalcitrant fluoroquinolone antibiotic norfloxacin. Environmental Technology & Innovation. 40. 104414–104414.
4.
Bissaro, Bastien, David Navarro, Éric Record, et al.. (2024). A New Phenolic Acid Decarboxylase from the Brown-Rot Fungus Neolentinus lepideus Natively Decarboxylates Biosourced Sinapic Acid into Canolol, a Bioactive Phenolic Compound. Bioengineering. 11(2). 181–181. 2 indexed citations
5.
Greff, Stéphane, Annick Turbé-Doan, Julien Lambert, et al.. (2024). Biotransformation of the Fluoroquinolone Antibiotic, Levofloxacin, by the Free and Immobilized Secretome of Coriolopsis gallica. Journal of Fungi. 10(12). 861–861.
6.
Lambert, Julien, Annick Turbé-Doan, Anne Lomascolo, et al.. (2024). Characterization of the Coriolopsis gallica DyP for Its Potential to Biotransform Various Fluoroquinolones. International Journal of Molecular Sciences. 25(21). 11392–11392. 1 indexed citations
7.
Darnet, Sylvain, et al.. (2024). Responses to and detoxification of esculin in white-rot fungi. Fungal Biology. 128(8). 2372–2380. 2 indexed citations
8.
Grisel, Sacha, Mireille Haon, David Navarro, et al.. (2022). The Maize Pathogen Ustilago maydis Secretes Glycoside Hydrolases and Carbohydrate Oxidases Directed toward Components of the Fungal Cell Wall. Applied and Environmental Microbiology. 88(23). e0158122–e0158122. 11 indexed citations
9.
Greff, Stéphane, Charlotte Simmler, Jean Armengaud, et al.. (2022). Biotransformation of the Fluoroquinolone, Levofloxacin, by the White-Rot Fungus Coriolopsis gallica. Journal of Fungi. 8(9). 965–965. 18 indexed citations
10.
Hadrich, Bilel, Giuliano Sciara, Anne Lomascolo, et al.. (2022). Optimization of the Decolorization of the Reactive Black 5 by a Laccase-like Active Cell-Free Supernatant from Coriolopsis gallica. Microorganisms. 10(6). 1137–1137. 12 indexed citations
11.
Ivaldi, Corinne, Mariane Daou, Laurent Vallon, et al.. (2021). Screening New Xylanase Biocatalysts from the Mangrove Soil Diversity. Microorganisms. 9(7). 1484–1484. 29 indexed citations
12.
Cerutti, Gabriele, Linda Celeste Montemiglio, Annick Turbé-Doan, et al.. (2021). Crystal structure and functional characterization of an oligosaccharide dehydrogenase from Pycnoporus cinnabarinus provides insights into fungal breakdown of lignocellulose. Biotechnology for Biofuels. 14(1). 161–161. 7 indexed citations
13.
Daou, Mariane, Amel Majira, Laurent Cézard, et al.. (2021). Fungal Treatment for the Valorization of Technical Soda Lignin. Journal of Fungi. 7(1). 39–39. 12 indexed citations
14.
Daou, Mariane, Mireille Haon, Betty Cottyn, et al.. (2021). A Putative Lignin Copper Oxidase from Trichoderma reesei. Journal of Fungi. 7(8). 643–643. 7 indexed citations
15.
Lebrigand, Kévin, Le He, Nishant Thakur, et al.. (2016). Comparative Genomic Analysis of Drechmeria coniospora Reveals Core and Specific Genetic Requirements for Fungal Endoparasitism of Nematodes. PLoS Genetics. 12(5). e1006017–e1006017. 32 indexed citations
16.
Kumar, Abhishek, Bernard Henrissat, Mikko Arvas, et al.. (2015). De Novo Assembly and Genome Analyses of the Marine-Derived Scopulariopsis brevicaulis Strain LF580 Unravels Life-Style Traits and Anticancerous Scopularide Biosynthetic Gene Cluster. PLoS ONE. 10(10). e0140398–e0140398. 29 indexed citations
17.
Poidevin, Laetitia, Jean‐Guy Berrin, Chloé Bennati-Granier, et al.. (2014). Comparative analyses of Podospora anserina secretomes reveal a large array of lignocellulose-active enzymes. Applied Microbiology and Biotechnology. 98(17). 7457–7469. 37 indexed citations
18.
Levasseur, Anthony, Sandrine Pagès, Henri‐Pierre Fierobe, et al.. (2004). Design and Production in Aspergillus niger of a Chimeric Protein Associating a Fungal Feruloyl Esterase and a Clostridial Dockerin Domain. Applied and Environmental Microbiology. 70(12). 6984–6991. 29 indexed citations
19.
Chamkha, Mohamed, Éric Record, Jean‐Louis Garcia, Marcel Asther, & Marc Labat. (2002). Isolation from a Shea Cake Digester of a Tannin-Tolerant Escherichia coli Strain Decarboxylating p -Hydroxybenzoic and Vanillic Acids. Current Microbiology. 44(5). 341–349. 23 indexed citations
20.
Bonnarme, Pascal, et al.. (1994). Fractionation of subcellular membranes of the secretory pathway from the peroxidase-producing white-rot fungusPhanerochaete chrysosporium. FEMS Microbiology Letters. 120(1-2). 155–161. 6 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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