M. Chevallay

635 total citations
22 papers, 481 citations indexed

About

M. Chevallay is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, M. Chevallay has authored 22 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in M. Chevallay's work include Muscle Physiology and Disorders (12 papers), Cardiomyopathy and Myosin Studies (5 papers) and Mitochondrial Function and Pathology (4 papers). M. Chevallay is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Cardiomyopathy and Myosin Studies (5 papers) and Mitochondrial Function and Pathology (4 papers). M. Chevallay collaborates with scholars based in France, United Kingdom and Italy. M. Chevallay's co-authors include F.M.S. Tomé, Michel Fardeau, Caroline A. Sewry, Jean Léger, Jocelyne Léger, Antonella Pini, F. Tomé, Luciano Merlini, B. Eymard and Giuseppe Gobbi and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Journal of the Neurological Sciences.

In The Last Decade

M. Chevallay

22 papers receiving 472 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Chevallay France 15 415 99 96 88 60 22 481
F. Tomé France 11 507 1.2× 59 0.6× 99 1.0× 85 1.0× 41 0.7× 15 584
Yeliz Yuva United Kingdom 8 567 1.4× 124 1.3× 149 1.6× 202 2.3× 35 0.6× 9 653
Bruno F. Gavassini Italy 9 352 0.8× 51 0.5× 122 1.3× 83 0.9× 23 0.4× 10 401
L. Feng United Kingdom 13 674 1.6× 122 1.2× 254 2.6× 107 1.2× 51 0.8× 19 795
Uno Kjörell Sweden 14 172 0.4× 95 1.0× 105 1.1× 82 0.9× 17 0.3× 26 423
Y. Sunada Japan 3 333 0.8× 84 0.8× 56 0.6× 76 0.9× 76 1.3× 4 364
Josette Dangain United Kingdom 8 350 0.8× 59 0.6× 67 0.7× 81 0.9× 8 0.1× 13 483
Alberto A. Zambon Italy 11 226 0.5× 32 0.3× 60 0.6× 61 0.7× 43 0.7× 26 324
U. L. Fairbrother United Kingdom 7 625 1.5× 64 0.6× 86 0.9× 141 1.6× 20 0.3× 10 817
Stephanie K. Mewborn United States 7 473 1.1× 102 1.0× 123 1.3× 44 0.5× 23 0.4× 7 596

Countries citing papers authored by M. Chevallay

Since Specialization
Citations

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

Fields of papers citing papers by M. Chevallay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Chevallay

This figure shows the co-authorship network connecting the top 25 collaborators of M. Chevallay. A scholar is included among the top collaborators of M. Chevallay 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 M. Chevallay. M. Chevallay 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.
He, Yi, Kristi Jones, Nicolas Vignier, et al.. (2001). Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study. Neurology. 57(7). 1319–1322. 24 indexed citations
2.
Fardeau, M, Patrick Vicart, A Caron, et al.. (2000). [Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene].. PubMed. 156(5). 497–504. 18 indexed citations
3.
Khurana, Tejvir S., Linda A. Specht, Alan H. Beggs, et al.. (1997). The Concomitant Use of Dystrophin and Utrophin/Dystrophin Related Protein Antibodies to Reduce Misdiagnosis of Duchenne/Becker Muscular Dystrophy. Biochemical and Biophysical Research Communications. 241(2). 232–235. 1 indexed citations
4.
Ferruzza, Emilia, et al.. (1996). Brain alterations in the classical form of congenital muscular dystrophy. Child s Nervous System. 12(10). 604–10. 23 indexed citations
5.
Pini, Antonella, Luciano Merlini, F. Tomé, M. Chevallay, & Giuseppe Gobbi. (1996). Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families. Brain and Development. 18(4). 316–322. 49 indexed citations
6.
Fardeau, Michel, A. Leclerc, Teresinha Evangelista, et al.. (1996). [Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].. PubMed. 152(1). 11–9. 28 indexed citations
7.
Laforêt, Pascal, Anne Lombès, B. Eymard, et al.. (1995). Chronic progressive external ophthalmoplegia with ragged-red fibers: Clinical, morphological and genetic investigations in 43 patients. Neuromuscular Disorders. 5(5). 399–413. 34 indexed citations
8.
Sewry, Caroline A., M. Chevallay, & F.M.S. Tomé. (1995). Expression of laminin subunits in human fetal skeletal muscle. The Histochemical Journal. 27(7). 497–504. 1 indexed citations
9.
Sewry, Caroline A., M. Chevallay, & F.M.S. Tomé. (1995). Expression of laminin subunits in human fetal skeletal muscle.. PubMed. 27(7). 497–504. 33 indexed citations
10.
Sewry, Caroline A., M. Chevallay, & F.M.S. Tomé. (1995). Expression of laminin subunits in human fetal skeletal muscle. The Histochemical Journal. 27(7). 497–504. 26 indexed citations
11.
Tomé, F.M.S., Kiichiro Matsumura, M. Chevallay, Kevin P. Campbell, & Michel Fardeau. (1994). Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study. Neuromuscular Disorders. 4(4). 343–348. 40 indexed citations
12.
Eymard, B., J C Brouet, H. Barry Collin, et al.. (1993). Late-onset rod myopathy associated with monoclonal gammopathy. Neuromuscular Disorders. 3(5-6). 557–560. 29 indexed citations
13.
Marini, Jean‐François, Françoise Pons, Jocelyne Léger, et al.. (1991). Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers. Neuromuscular Disorders. 1(6). 397–409. 44 indexed citations
14.
Soussi‐Yanicostas, Nadia, M. Chevallay, Christine Laurent‐Winter, et al.. (1991). Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy. Neuromuscular Disorders. 1(2). 103–111. 22 indexed citations
15.
Gayraud, M., F. Tomé, S. Herson, et al.. (1989). [Histopathologic aspects of polymyositis and dermatomyositis. Correlation with the clinical course. Study of 57 cases].. PubMed. 140(6). 445–8. 2 indexed citations
16.
Tomé, F.M.S., Richard Tegnér, & M. Chevallay. (1988). VARICOSITIES IN HUMAN FETAL SCIATIC NERVE FIBRES. Neuropathology and Applied Neurobiology. 14(6). 495–504. 2 indexed citations
17.
Pons, F., Jocelyne Léger, M. Chevallay, et al.. (1986). Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles. Journal of the Neurological Sciences. 76(2-3). 151–163. 53 indexed citations
18.
Tomé, F.M.S., Michel Fardeau, Pierre Lebon, & M. Chevallay. (1981). Inclusion Body Myositis. PubMed. 38(22). 287–291. 31 indexed citations
19.
Godeau, P, et al.. (1977). [Neuropathy due to chloroquine in lupus erythematosus. 2 recent cases, emphasizing the necessity for ultrastructural study of the muscle biopsy].. PubMed. 127(8-9). 544–51. 3 indexed citations
20.
Flament-Durand, J, et al.. (1973). [Nemaline myopathy. Clinical, histological, ultrastructural and anatomical data concerning a new case with fatal course due to respiratory insufficiency].. PubMed. 30(5). 505–26. 1 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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