Michel Vivaudou

2.2k total citations
57 papers, 1.7k citations indexed

About

Michel Vivaudou is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine. According to data from OpenAlex, Michel Vivaudou has authored 57 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 19 papers in Pathology and Forensic Medicine. Recurrent topics in Michel Vivaudou's work include Ion channel regulation and function (37 papers), Cardiac Ischemia and Reperfusion (19 papers) and Cardiac electrophysiology and arrhythmias (16 papers). Michel Vivaudou is often cited by papers focused on Ion channel regulation and function (37 papers), Cardiac Ischemia and Reperfusion (19 papers) and Cardiac electrophysiology and arrhythmias (16 papers). Michel Vivaudou collaborates with scholars based in France, United States and Germany. Michel Vivaudou's co-authors include Christophe Moreau, Kim W. Chan, John V. Walsh, Jinliang Sui, Lucie H. Clapp, Joshua J. Singer, Diomedes E. Logothetis, Cyrille Forestier, Nathalie Picollet-D’hahan and Hélène Jacquet and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Michel Vivaudou

57 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
Michel Vivaudou France 23 1.2k 640 520 391 159 57 1.7k
Heinz Gögelein Germany 30 1.9k 1.5× 878 1.4× 469 0.9× 1.1k 2.8× 235 1.5× 55 2.8k
Y Kurachi Japan 28 1.9k 1.5× 878 1.4× 933 1.8× 1.2k 3.2× 313 2.0× 47 2.7k
Noel W. Davies United Kingdom 25 1.9k 1.6× 1.1k 1.8× 716 1.4× 970 2.5× 155 1.0× 36 2.8k
F M Ashcroft United Kingdom 11 1.1k 0.9× 632 1.0× 226 0.4× 254 0.6× 68 0.4× 38 1.7k
G. Trube Germany 11 1.6k 1.3× 983 1.5× 352 0.7× 910 2.3× 80 0.5× 20 1.9k
Elena Makhina United States 11 1.4k 1.2× 756 1.2× 256 0.5× 727 1.9× 40 0.3× 14 1.6k
Anatoli N. Lopatin United States 24 2.8k 2.3× 1.4k 2.2× 285 0.5× 1.8k 4.6× 61 0.4× 47 3.4k
M. C. Capogrossi United States 18 1.1k 0.9× 547 0.9× 277 0.5× 897 2.3× 79 0.5× 33 1.5k
Johan Vereecke Belgium 34 2.2k 1.8× 1.1k 1.7× 278 0.5× 1.5k 3.7× 65 0.4× 83 3.0k
Harley T. Kurata Canada 24 1.4k 1.1× 677 1.1× 149 0.3× 686 1.8× 43 0.3× 68 1.8k

Countries citing papers authored by Michel Vivaudou

Since Specialization
Citations

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

Fields of papers citing papers by Michel Vivaudou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michel Vivaudou

This figure shows the co-authorship network connecting the top 25 collaborators of Michel Vivaudou. A scholar is included among the top collaborators of Michel Vivaudou 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 Vivaudou. Michel Vivaudou 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.
Chassot, Anne‐Amandine, Nadine Thézé, Dmitrii Zabelskii, et al.. (2024). Hijacking of internal calcium dynamics by intracellularly residing viral rhodopsins. Nature Communications. 15(1). 65–65. 9 indexed citations
2.
Bolla, Jean‐Michel, et al.. (2017). Providencia stuartii form biofilms and floating communities of cells that display high resistance to environmental insults. PLoS ONE. 12(3). e0174213–e0174213. 15 indexed citations
3.
Godet, Anne-Claire, et al.. (2017). Functional mapping of the N-terminal arginine cluster and C-terminal acidic residues of Kir6.2 channel fused to a G protein-coupled receptor. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1859(10). 2144–2153. 2 indexed citations
4.
Martel, Anne, Lucas Antony, Yuri Gerelli, et al.. (2016). Membrane Permeation versus Amyloidogenicity: A Multitechnique Study of Islet Amyloid Polypeptide Interaction with Model Membranes. Journal of the American Chemical Society. 139(1). 137–148. 48 indexed citations
5.
Dupuis, Julien P., et al.. (2015). Kir6.2 activation by sulfonylurea receptors: a different mechanism of action for SUR1 and SUR2A subunits via the same residues. Physiological Reports. 3(9). e12533–e12533. 12 indexed citations
6.
Cherezov, Vadim, et al.. (2013). Functional Assay for T4 Lysozyme-Engineered G Protein-Coupled Receptors with an Ion Channel Reporter. Structure. 22(1). 149–155. 9 indexed citations
7.
Sierra, Ana, Zhiyong Zhu, Nicolas Sapay, et al.. (2012). Regulation of Cardiac ATP-sensitive Potassium Channel Surface Expression by Calcium/Calmodulin-dependent Protein Kinase II. Journal of Biological Chemistry. 288(3). 1568–1581. 22 indexed citations
8.
Jacquet, Hélène, et al.. (2010). Recognition of Sulfonylurea Receptor (ABCC8/9) Ligands by the Multidrug Resistance Transporter P-glycoprotein (ABCB1). Journal of Biological Chemistry. 286(5). 3552–3569. 24 indexed citations
9.
Lydia, Ng, et al.. (2010). Design of Biosensors Based on the Covalent Assembly of G-Protein Coupled Receptors and Potassium Channels. Biophysical Journal. 98(3). 193a–193a. 1 indexed citations
10.
Dupuis, Julien P., et al.. (2008). Three C‐terminal residues from the sulphonylurea receptor contribute to the functional coupling between the KATP channel subunits SUR2A and Kir6.2. The Journal of Physiology. 586(13). 3075–3085. 18 indexed citations
11.
Wang, Chuan, Ke Yang, Kun Fang, et al.. (2008). Coassembly of Different Sulfonylurea Receptor Subtypes Extends the Phenotypic Diversity of ATP-sensitive Potassium (KATP) Channels. Molecular Pharmacology. 74(5). 1333–1344. 33 indexed citations
12.
Arumugam, K., et al.. (2007). Adaptive torsion-angle quasi-statics: a general simulation method with applications to protein structure analysis and design. Bioinformatics. 23(13). i408–i417. 24 indexed citations
13.
Melin, Patricia, Eric Hosy, Michel Vivaudou, & Frédéric Becq. (2007). CFTR inhibition by glibenclamide requires a positive charge in cytoplasmic loop three. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1768(10). 2438–2446. 16 indexed citations
14.
Waard, Michel De, et al.. (2006). Hourglass SiO2 coating increases the performance of planar patch-clamp. Journal of Biotechnology. 125(1). 142–154. 35 indexed citations
15.
Bloc, Alain, et al.. (2004). Zinc is both an intracellular and extracellular regulator of KATP channel function. The Journal of Physiology. 559(1). 157–167. 54 indexed citations
16.
Dérand, Renaud, et al.. (2003). Inhibition of ATP-sensitive K+ channels by substituted benzo[c]quinolizinium CFTR activators. Biochemical Pharmacology. 66(3). 425–430. 9 indexed citations
17.
Forestier, Cyrille, et al.. (1996). Mechanism of action of K channel openers on skeletal muscle KATP channels. Interactions with nucleotides and protons.. The Journal of General Physiology. 107(4). 489–502. 23 indexed citations
18.
Chan, Kim W., Jinliang Sui, Michel Vivaudou, & Diomedes E. Logothetis. (1996). Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K + channel  subunit. Proceedings of the National Academy of Sciences. 93(24). 14193–14198. 101 indexed citations
19.
Vivaudou, Michel, Christophe Arnoult, & Michel Villaz. (1991). Skeletal muscle ATP-sensitive K+ channels recorded from sarcolemmal blebs of split fibers: ATP inhibition is reduced by magnesium and ADP. The Journal of Membrane Biology. 122(2). 165–175. 68 indexed citations
20.
Clapp, Lucie H., Michel Vivaudou, John V. Walsh, & J J Singer. (1987). Acetylcholine increases voltage-activated Ca2+ current in freshly dissociated smooth muscle cells.. Proceedings of the National Academy of Sciences. 84(7). 2092–2096. 64 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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