Patrick Cottin

2.0k total citations
58 papers, 1.7k citations indexed

About

Patrick Cottin is a scholar working on Cell Biology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Patrick Cottin has authored 58 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Cell Biology, 48 papers in Molecular Biology and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Patrick Cottin's work include Calpain Protease Function and Regulation (47 papers), Muscle Physiology and Disorders (25 papers) and RNA regulation and disease (9 papers). Patrick Cottin is often cited by papers focused on Calpain Protease Function and Regulation (47 papers), Muscle Physiology and Disorders (25 papers) and RNA regulation and disease (9 papers). Patrick Cottin collaborates with scholars based in France, Morocco and United States. Patrick Cottin's co-authors include Sylvie Poussard, André Ducastaing, Jean‐Jacques Brustis, J.J. Brustis, Élise Dargelos, Stéphane Dedieu, Denis Balcerzak, Laetitia Daury, Cédric Brulé and Nathalie Dourdin and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Molecular Biology and Biochemical Journal.

In The Last Decade

Patrick Cottin

57 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick Cottin France 26 1.2k 1.1k 354 281 257 58 1.7k
André Ducastaing France 21 872 0.7× 798 0.8× 285 0.8× 200 0.7× 313 1.2× 42 1.3k
Sylvie Poussard France 24 938 0.8× 756 0.7× 273 0.8× 202 0.7× 103 0.4× 41 1.3k
Yoshihide Ikeuchi Japan 26 1.2k 1.0× 392 0.4× 207 0.6× 489 1.7× 280 1.1× 78 2.0k
H Sugita Japan 16 968 0.8× 403 0.4× 259 0.7× 225 0.8× 71 0.3× 39 1.3k
Masashi Kusubata Japan 22 819 0.7× 470 0.4× 206 0.6× 105 0.4× 61 0.2× 49 1.5k
Yasuko Hagiwara Japan 21 1.6k 1.3× 535 0.5× 403 1.1× 353 1.3× 34 0.1× 42 1.9k
F. P. Moss Australia 10 1.1k 0.9× 305 0.3× 149 0.4× 300 1.1× 219 0.9× 15 1.5k
Marc Bartoli France 32 2.3k 1.9× 757 0.7× 544 1.5× 347 1.2× 34 0.1× 89 2.8k
Quan Yang China 17 1.2k 1.0× 168 0.2× 121 0.3× 324 1.2× 29 0.1× 46 1.7k
Michael Ferns United States 20 1.5k 1.2× 631 0.6× 826 2.3× 175 0.6× 11 0.0× 45 1.8k

Countries citing papers authored by Patrick Cottin

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Cottin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Cottin

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick Cottin. A scholar is included among the top collaborators of Patrick Cottin 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 Patrick Cottin. Patrick Cottin 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.
Stuelsatz, Pascal, Frédéric Pouzoulet, Yann Lamarre, et al.. (2010). Down-regulation of MyoD by Calpain 3 Promotes Generation of Reserve Cells in C2C12 Myoblasts. Journal of Biological Chemistry. 285(17). 12670–12683. 43 indexed citations
2.
Dargelos, Élise, Cédric Brulé, Lydie Combaret, et al.. (2007). Involvement of the calcium-dependent proteolytic system in skeletal muscle aging. Experimental Gerontology. 42(11). 1088–1098. 32 indexed citations
3.
Goudenege, Sébastien, Élise Dargelos, Stéphane Claverol, et al.. (2007). Comparative proteomic analysis of myotube caveolae after milli‐calpain deregulation. PROTEOMICS. 7(18). 3289–3298. 16 indexed citations
4.
Leloup, Ludovic, et al.. (2006). Myoblast attachment and spreading are regulated by different patterns by ubiquitous calpains. Cell Motility and the Cytoskeleton. 63(4). 193–207. 23 indexed citations
5.
Poussard, Sylvie, et al.. (2003). MAP Kinase-dependent Degradation of p27Kip1 by Calpains in Choroidal Melanoma Cells. Journal of Biological Chemistry. 278(14). 12443–12451. 50 indexed citations
6.
Dedieu, Stéphane, Sylvie Poussard, Florence Grise, et al.. (2003). Myoblast migration is regulated by calpain through its involvement in cell attachment and cytoskeletal organization. Experimental Cell Research. 292(1). 187–200. 97 indexed citations
7.
Dedieu, Stéphane, et al.. (2003). Myoblast migration is prevented by a calpain‐dependent accumulation of MARCKS. Biology of the Cell. 95(9). 615–623. 33 indexed citations
8.
Dedieu, Stéphane, et al.. (2002). Involvement of myogenic regulator factors during fusion in the cell line C2C12. The International Journal of Developmental Biology. 46(2). 235–241. 111 indexed citations
9.
Dargelos, Élise, Stéphane Dedieu, Philippe Veschambre, et al.. (2002). Development of an inducible system to assess p94 (CAPN3) function in cultured muscle cells. Journal of Biotechnology. 96(3). 271–279. 12 indexed citations
10.
Poussard, Sylvie, Sandrine Dulong, J.J. Brustis, et al.. (2001). Evidence for a MARCKS–PKCα complex in skeletal muscle. The International Journal of Biochemistry & Cell Biology. 33(7). 711–721. 13 indexed citations
11.
Dourdin, Nathalie, et al.. (2000). M-calpain levels increase during fusion of myoblasts in the mutant muscular dysgenesis (mdg) mouse. The International Journal of Developmental Biology. 44(4). 421–428. 13 indexed citations
12.
Verret, C., Sylvie Poussard, Katia Touyarot, et al.. (1999). Degradation of protein kinase Mα by μ-calpain in a μ-calpain-protein kinase Cα complex. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1430(1). 141–148. 9 indexed citations
13.
Cottin, Patrick, et al.. (1999). Pressure effects on proteolysis catalysed by calpain. IUBMB Life. 47(1). 25–36. 3 indexed citations
14.
Dourdin, Nathalie, Denis Balcerzak, J.J. Brustis, et al.. (1999). Potential m-Calpain Substrates during Myoblast Fusion. Experimental Cell Research. 246(2). 433–442. 54 indexed citations
15.
Balcerzak, Denis, et al.. (1998). Calpastatin-modulation of m-calpain activity is required for myoblast fusion. European Journal of Cell Biology. 75(3). 247–253. 40 indexed citations
16.
Dourdin, Nathalie, Jean‐Jacques Brustis, Denis Balcerzak, et al.. (1997). Myoblast Fusion Requires Fibronectin Degradation by Exteriorized m-Calpain. Experimental Cell Research. 235(2). 385–394. 51 indexed citations
17.
Cottin, Patrick, Sylvie Poussard, Dominique Mornet, et al.. (1992). In vitro digestion of dystrophin by calcium-dependent proteases, calpains I and II. Biochimie. 74(6). 565–570. 32 indexed citations
18.
Cottin, Patrick, et al.. (1991). Free calcium and calpain I activity. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1079(2). 139–145. 34 indexed citations
19.
Cottin, Patrick, et al.. (1988). Evidence for a Ca2+‐independent association between calpain II and phospholipid vesicles. FEBS Letters. 227(2). 209–214. 15 indexed citations
20.
Cottin, Patrick, et al.. (1981). Ca2+‐dependent association between a Ca2+‐activated neutral proteinase (CaANP) and its specific inhibitor. FEBS Letters. 136(2). 221–224. 46 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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