Didier Roche

987 total citations
31 papers, 608 citations indexed

About

Didier Roche is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Didier Roche has authored 31 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Organic Chemistry and 4 papers in Pharmacology. Recurrent topics in Didier Roche's work include Chemical Synthesis and Analysis (14 papers), Microbial Natural Products and Biosynthesis (4 papers) and Synthetic Organic Chemistry Methods (4 papers). Didier Roche is often cited by papers focused on Chemical Synthesis and Analysis (14 papers), Microbial Natural Products and Biosynthesis (4 papers) and Synthetic Organic Chemistry Methods (4 papers). Didier Roche collaborates with scholars based in France, United Kingdom and Switzerland. Didier Roche's co-authors include Oljan Repič, Kapa Prasad, Jean‐Yves Ortholand, Janine Cossy, Véronique Bellosta, Renaud Prudent, Thomas J. Blacklock, D. Allen Annis, Peter J. Dandliker and Adam Nelson and has published in prestigious journals such as Nucleic Acids Research, Chemical Communications and Journal of Medicinal Chemistry.

In The Last Decade

Didier Roche

31 papers receiving 589 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Didier Roche France 15 377 268 76 56 52 31 608
Sarah J. Fink United States 13 347 0.9× 179 0.7× 76 1.0× 29 0.5× 38 0.7× 19 547
Priyadeep Bhutani India 8 445 1.2× 188 0.7× 68 0.9× 39 0.7× 32 0.6× 18 701
Panagiota Moutevelis‐Minakakis Greece 14 296 0.8× 345 1.3× 46 0.6× 84 1.5× 49 0.9× 28 554
Scott A. Frank United States 14 636 1.7× 209 0.8× 102 1.3× 27 0.5× 54 1.0× 27 781
Andrej Boháč Slovakia 12 300 0.8× 167 0.6× 71 0.9× 29 0.5× 58 1.1× 45 516
Zhao‐Kui Wan United States 19 715 1.9× 397 1.5× 71 0.9× 35 0.6× 42 0.8× 31 1.0k
Keith C. Ellis United States 15 300 0.8× 309 1.2× 69 0.9× 21 0.4× 79 1.5× 28 682
Carl Berthelette Canada 19 428 1.1× 200 0.7× 64 0.8× 32 0.6× 84 1.6× 25 705
Bodo Scheiper Germany 12 609 1.6× 242 0.9× 100 1.3× 55 1.0× 62 1.2× 13 863
Alexander G. Godfrey United States 10 338 0.9× 201 0.8× 50 0.7× 66 1.2× 57 1.1× 19 590

Countries citing papers authored by Didier Roche

Since Specialization
Citations

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

Fields of papers citing papers by Didier Roche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Didier Roche

This figure shows the co-authorship network connecting the top 25 collaborators of Didier Roche. A scholar is included among the top collaborators of Didier Roche 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 Didier Roche. Didier Roche 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.
Balavoine, Fabrice, Frédéric Miege, Nadia De Mota, et al.. (2024). Rational design, synthesis and pharmacological characterization of novel aminopeptidase A inhibitors. Bioorganic & Medicinal Chemistry Letters. 113. 129940–129940. 1 indexed citations
2.
Prudent, Renaud, et al.. (2023). Affinity selection mass spectrometry speeding drug discovery. Drug Discovery Today. 28(11). 103760–103760. 23 indexed citations
3.
Lindberg, Mattias F., Frédéric Miege, Didier Roche, et al.. (2023). Leucettinibs, a Class of DYRK/CLK Kinase Inhibitors Inspired by the Marine Sponge Natural Product Leucettamine B. Journal of Medicinal Chemistry. 66(15). 10694–10714. 15 indexed citations
4.
Prudent, Renaud, D. Allen Annis, Peter J. Dandliker, Jean‐Yves Ortholand, & Didier Roche. (2020). Exploring new targets and chemical space with affinity selection-mass spectrometry. Nature Reviews Chemistry. 5(1). 62–71. 58 indexed citations
5.
Morgentin, Rémy, Mark Dow, A. Aimon, et al.. (2018). Translation of innovative chemistry into screening libraries: an exemplar partnership from the European Lead Factory. Drug Discovery Today. 23(9). 1578–1583. 11 indexed citations
6.
Chantalat, L., Jean‐François Fournier, Marcus Gastreich, et al.. (2017). New Caspase-1 inhibitor by scaffold hopping into bio-inspired 3D-fragment space. Bioorganic & Medicinal Chemistry Letters. 27(24). 5373–5377. 7 indexed citations
7.
Fournier, Jean‐François, et al.. (2016). An expedient synthesis of non-racemic N-alkylated pyrrolidin-2,5-diones and piperidin-2,6-diones as peptidomimetics. Tetrahedron Letters. 57(52). 5924–5927. 2 indexed citations
8.
Nelson, Adam & Didier Roche. (2015). Innovative approaches to the design and synthesis of small molecule libraries. Bioorganic & Medicinal Chemistry. 23(11). 2613–2613. 14 indexed citations
9.
Aimon, A., Mark Dow, Nicolas Fleury‐Brégeot, et al.. (2014). Design, synthesis and decoration of molecular scaffolds for exploitation in the production of alkaloid-like libraries. Bioorganic & Medicinal Chemistry. 23(11). 2629–2635. 25 indexed citations
10.
Valeur, Eric, Djordje Müsil, L Doaré, et al.. (2012). Structure-based design of 7-azaindole-pyrrolidine amides as inhibitors of 11β-hydroxysteroid dehydrogenase type I. Bioorganic & Medicinal Chemistry Letters. 22(18). 5909–5914. 11 indexed citations
11.
Bellosta, Véronique, et al.. (2012). Rhodium(iii)-catalyzed allylic C–H bond amination. Synthesis of cyclic amines from ω-unsaturated N-sulfonylamines. Chemical Communications. 48(87). 10745–10745. 87 indexed citations
12.
Baron, Anne, et al.. (2011). Synthesis and biological properties of macrolactam analogs of the natural product macrolide (−)-A26771B. Bioorganic & Medicinal Chemistry Letters. 21(16). 4768–4772. 20 indexed citations
13.
Roche, Didier, Caroline Leriche, L Doaré, et al.. (2009). Discovery and structure-guided drug design of inhibitors of 11β-hydroxysteroid-dehydrogenase type I based on a spiro-carboxamide scaffold. Bioorganic & Medicinal Chemistry Letters. 19(13). 3682–3685. 21 indexed citations
14.
Roche, Didier, Caroline Leriche, L Doaré, et al.. (2009). Discovery and structure–activity relationships of pentanedioic acid diamides as potent inhibitors of 11β-hydroxysteroid dehydrogenase type I. Bioorganic & Medicinal Chemistry Letters. 19(10). 2674–2678. 13 indexed citations
15.
Wattanasin, Sompong, Rainer Albert, Claus Ehrhardt, et al.. (2003). 1,4-Diazepane-2-ones as novel inhibitors of LFA-1. Bioorganic & Medicinal Chemistry Letters. 13(3). 499–502. 40 indexed citations
16.
Wattanasin, Sompong, Beat Weidmann, Didier Roche, et al.. (2001). Design and Synthesis of Potent and Selective Inhibitors of Integrin VLA-4. Bioorganic & Medicinal Chemistry Letters. 11(22). 2955–2958. 11 indexed citations
17.
Roche, Didier, et al.. (2001). Stereoselective synthesis of 2-amino-5-hydroxycaprolactams from l-glutamic acid. Tetrahedron Letters. 42(8). 1459–1462. 6 indexed citations
18.
Roche, Didier, Kapa Prasad, & Oljan Repič. (1999). ChemInform Abstract: Enantioselective Acylation of β‐Aminoesters Using Penicillin G Acylase in Organic Solvents.. ChemInform. 30(31). 1 indexed citations
19.
Roche, Didier, et al.. (1998). Synthesis of benzylated (R)- and as conformationally restricted building blocks for the preparation of E- and P-selectin antagonists. Tetrahedron Letters. 39(17). 2545–2548. 8 indexed citations
20.
Solladié‐Cavallo, Arlette, Didier Roche, Guido Bold, et al.. (1996). Stereoselective synthesis of (4S,5R,6S)-4-(5,6-epoxy-6-phenyl)-γ-lactone. Tetrahedron Asymmetry. 7(6). 1797–1810. 4 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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