Michel Véron

3.2k total citations
79 papers, 2.5k citations indexed

About

Michel Véron is a scholar working on Molecular Biology, Materials Chemistry and Cell Biology. According to data from OpenAlex, Michel Véron has authored 79 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 23 papers in Materials Chemistry and 16 papers in Cell Biology. Recurrent topics in Michel Véron's work include Mechanisms of cancer metastasis (25 papers), Cancer Mechanisms and Therapy (14 papers) and MXene and MAX Phase Materials (13 papers). Michel Véron is often cited by papers focused on Mechanisms of cancer metastasis (25 papers), Cancer Mechanisms and Therapy (14 papers) and MXene and MAX Phase Materials (13 papers). Michel Véron collaborates with scholars based in France, United States and United Kingdom. Michel Véron's co-authors include Fabrice Agou, Joël Janin, Dominique Deville‐Bonne, Georges N. Cohen, Benoı̂t Schneider, François Traincard, Marie‐Noëlle Simon, Jean de Gunzburg, Alain Israël and Robert R. Kay and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Michel Véron

78 papers receiving 2.4k citations

Peers

Michel Véron

Mary E. McGrath United States

Ujwal Shinde United States

Mark O. J. Olson United States

Martin L. Phillips United States

Philip Furmanski United States

Christian Schölz Germany

Hans‐Joachim Fritz Germany

Youri I. Pavlov United States

Luitzen de Jong Netherlands

Mary L. Stephenson United States

Mary E. McGrath United States

Michel Véron

1.6k ×1.0

128 ×0.3

341 ×0.9

154 ×0.4

202 ×0.7

Citations per year, relative to Michel Véron Michel Véron (= 1×) peers Mary E. McGrath

Countries citing papers authored by Michel Véron

Since Specialization

Citations

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

Fields of papers citing papers by Michel Véron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michel Véron

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Chiaravalli, Jeanne, Hafida Fsihi, Yves‐Marie Coïc, et al.. (2011). Direct inhibition of NF-κB activation by peptide targeting the NOA ubiquitin binding domain of NEMO. Biochemical Pharmacology. 82(9). 1163–1174. 12 indexed citations

Grubisha, Olivera, M. Kamińska, S. Duquerroy, et al.. (2009). DARPin-Assisted Crystallography of the CC2-LZ Domain of NEMO Reveals a Coupling between Dimerization and Ubiquitin Binding. Journal of Molecular Biology. 395(1). 89–104. 34 indexed citations

Traincard, François, et al.. (2007). NEMO oligomerization in the dynamic assembly of the IκB kinase core complex. FEBS Journal. 274(10). 2540–2551. 32 indexed citations

Galetto, Román, et al.. (2005). Dissection of a Circumscribed Recombination Hot Spot in HIV-1 after a Single Infectious Cycle. Journal of Biological Chemistry. 281(5). 2711–2720. 37 indexed citations

Agou, Fabrice, Gilles Courtois, Jeanne Chiaravalli, et al.. (2004). Inhibition of NF-κB Activation by Peptides Targeting NF-κB Essential Modulator (NEMO) Oligomerization. Journal of Biological Chemistry. 279(52). 54248–54257. 52 indexed citations

Traincard, François, et al.. (2004). Specific inhibition of AGC protein kinases by antibodies against C‐terminal epitopes. FEBS Letters. 572(1-3). 276–280. 2 indexed citations

Galetto, Román, et al.. (2004). The Structure of HIV-1 Genomic RNA in the gp120 Gene Determines a Recombination Hot Spot in Vivo. Journal of Biological Chemistry. 279(35). 36625–36632. 61 indexed citations

Gallois‐Montbrun, Sarah, Yuxing Chen, Hélène Dutartre, et al.. (2003). Structural Analysis of the Activation of Ribavirin Analogs by NDP Kinase: Comparison with Other Ribavirin Targets. Molecular Pharmacology. 63(3). 538–546. 24 indexed citations

Biondi, Ricardo M., et al.. (2003). Random Insertion of Green Fluorescent Protein into the Regulatory Subunit of Cyclic Adenosine Monophosphate-Dependent Protein Kinase. Humana Press eBooks. 183. 57–68. 3 indexed citations

10.

Gallois‐Montbrun, Sarah, et al.. (2003). Reaction of human UMP‐CMP kinase with natural and analog substrates. European Journal of Biochemistry. 270(8). 1784–1790. 36 indexed citations

11.

Schneider, Benoı̂t, et al.. (2002). Nucleotide affinity for a stable phosphorylated intermediate of nucleoside diphosphate kinase. Protein Science. 11(7). 1648–1656. 3 indexed citations

12.

Agou, Fabrice, et al.. (1998). Coupling between Catalysis and Oligomeric Structure in Nucleoside Diphosphate Kinase. Journal of Biological Chemistry. 273(8). 4436–4442. 39 indexed citations

13.

Aguado‐Velasco, Carmen, et al.. (1996). NDP kinase can modulate contraction ofDictyostelium cytoskeletons. Cell Motility and the Cytoskeleton. 34(3). 194–205. 4 indexed citations

14.

Bourdais, Julie, Ricardo M. Biondi, Simon Sarfati, et al.. (1996). Cellular Phosphorylation of Anti-HIV Nucleosides. Journal of Biological Chemistry. 271(14). 7887–7890. 74 indexed citations

15.

Véron, Michel, Annemiek D. Tepper, Martin Hildebrandt, et al.. (1995). Nucleoside Diphosphate Kinase: an Old Enzyme with New Functions?. Advances in experimental medicine and biology. 370. 607–611. 6 indexed citations

16.

Sellam, Olivier, Michel Véron, & Martin Hildebrandt. (1995). Overexpression of wild‐type and mutant NDP kinase in Dictyostelium discoideum. Molecular Microbiology. 16(1). 79–85. 8 indexed citations

17.

Bominaar, Anthony A., Annemiek D. Tepper, & Michel Véron. (1994). Autophosphorylation of nucleoside diphosphate kinase on non‐histidine residues. FEBS Letters. 353(1). 5–8. 35 indexed citations

18.

Simon, Marie‐Noëlle, et al.. (1992). Serine/threonine protein phosphatases in Dictyostelium discoideum: No evidence for type I activity. Biochemical and Biophysical Research Communications. 184(3). 1142–1151. 8 indexed citations

19.

Dumas, Christian, et al.. (1991). Crystallization and preliminary X-ray diffraction studies of nucleoside diphosphate kinase from Dictyostelium discoideum. Journal of Molecular Biology. 217(2). 239–240. 8 indexed citations

20.

Guitton, Marie-Christine, et al.. (1988). Cloning of a cDNA for the S-adenosyl-l-homocysteine hydrolase from Dictyostelium discoideum. Biochimie. 70(6). 835–840. 5 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.

Explore authors with similar magnitude of impact