Marc Bartoli

4.0k total citations
89 papers, 2.8k citations indexed

About

Marc Bartoli is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marc Bartoli has authored 89 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 22 papers in Cell Biology and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marc Bartoli's work include Muscle Physiology and Disorders (49 papers), Calpain Protease Function and Regulation (14 papers) and RNA Research and Splicing (14 papers). Marc Bartoli is often cited by papers focused on Muscle Physiology and Disorders (49 papers), Calpain Protease Function and Regulation (14 papers) and RNA Research and Splicing (14 papers). Marc Bartoli collaborates with scholars based in France, United States and Lebanon. Marc Bartoli's co-authors include Isabelle Richard, Isabelle Richard, Nicolas Lévy, Nathalie Bourg, Martin Krahn, Carinne Roudaut, Ariane Monneron, Stéphanie Duguez, Francis Castets and Nathalie Danièle and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Circulation.

In The Last Decade

Marc Bartoli

84 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marc Bartoli France 32 2.3k 757 544 488 428 89 2.8k
Motoi Kanagawa Japan 28 2.9k 1.3× 693 0.9× 794 1.5× 446 0.9× 261 0.6× 73 3.6k
Svetlana Bezprozvannaya United States 27 3.3k 1.5× 368 0.5× 436 0.8× 214 0.4× 528 1.2× 43 4.0k
Elizabeth Vafiadaki Greece 22 1.5k 0.7× 303 0.4× 311 0.6× 226 0.5× 708 1.7× 40 2.0k
E. Bonilla United States 40 4.8k 2.1× 271 0.4× 771 1.4× 256 0.5× 325 0.8× 76 5.4k
Louise V.B. Anderson United Kingdom 31 2.7k 1.2× 773 1.0× 844 1.6× 233 0.5× 600 1.4× 53 3.0k
Stephen J. Crocker United States 34 2.0k 0.9× 470 0.6× 903 1.7× 220 0.5× 141 0.3× 72 4.1k
F S Walsh United Kingdom 32 1.8k 0.8× 403 0.5× 809 1.5× 282 0.6× 204 0.5× 56 2.8k
Xin‐Ming Shen United States 31 1.3k 0.6× 907 1.2× 387 0.7× 208 0.4× 113 0.3× 79 2.6k
Martine Pinçon‐Raymond France 28 1.5k 0.7× 445 0.6× 554 1.0× 225 0.5× 190 0.4× 61 2.3k
Karl J. A. McCullagh Ireland 20 1.9k 0.8× 652 0.9× 278 0.5× 223 0.5× 241 0.6× 29 2.6k

Countries citing papers authored by Marc Bartoli

Since Specialization
Citations

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

Fields of papers citing papers by Marc Bartoli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Bartoli

This figure shows the co-authorship network connecting the top 25 collaborators of Marc Bartoli. A scholar is included among the top collaborators of Marc Bartoli 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 Marc Bartoli. Marc Bartoli 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.
Cintas, Pascal, Olivier Dellis, Charles Van Goethem, et al.. (2024). Store-operated calcium entry dysfunction in CRAC channelopathy: Insights from a novel STIM1 mutation. Clinical Immunology. 265. 110306–110306. 1 indexed citations
2.
Brocard, Cécile, et al.. (2024). Knockdown of calpain1 in lumbar motoneurons reduces spasticity after spinal cord injury in adult rats. Molecular Therapy. 32(4). 1096–1109. 4 indexed citations
3.
4.
Courrier, Sébastien, Nathalie Da Silva, Martin Krahn, et al.. (2023). A Dysferlin Exon 32 Nonsense Mutant Mouse Model Shows Pathological Signs of Dysferlinopathy. Biomedicines. 11(5). 1438–1438. 3 indexed citations
5.
Roeckel-Trévisiol, Nathalie, Frédérique Lembo, Nicolas Lenfant, et al.. (2022). Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot–Marie–Tooth disease 4H. Brain. 146(5). 1844–1858. 9 indexed citations
6.
Skrypnyk, Cristina, Nathalie Da Silva, Jon Andoni Urtizberea, et al.. (2021). A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases. Clinical Genetics. 100(1). 84–89. 5 indexed citations
7.
Bartoli, Marc, Nathalie Bonello‐Palot, Christophe Pécheux, et al.. (2021). Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients. Genetics in Medicine. 23(8). 1574–1577. 14 indexed citations
8.
Skrypnyk, Cristina, Nathalie Da Silva, Nicolas Lévy, et al.. (2021). A novel bi-allelic loss-of-function mutation in STIM1 expands the phenotype of STIM1-related diseases. HAL (Le Centre pour la Communication Scientifique Directe).
9.
Bartoli, Marc, et al.. (2020). CRISP(R)ation musculaire. médecine/sciences. 36(4). 358–366.
10.
Salort‐Campana, Emmanuelle, Svetlana Gorokhova, Nathalie Bonello‐Palot, et al.. (2020). Refining NGS diagnosis of muscular disorders. Journal of Neurology Neurosurgery & Psychiatry. 92(2). 223–225. 1 indexed citations
11.
Bernard‐Marissal, Nathalie, Éliane Chouery, Jean‐Pierre Desvignes, et al.. (2019). Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1. Human Molecular Genetics. 28(14). 2378–2394. 16 indexed citations
12.
Barthélémy, Florian, Sébastien Courrier, Nicolas Lévy, Martin Krahn, & Marc Bartoli. (2018). Dysferlin Exon 32 Skipping in Patient Cells. Methods in molecular biology. 1828. 489–496. 3 indexed citations
13.
Gorokhova, Svetlana, Anthony Béhin, Jon Andoni Urtizberea, et al.. (2015). Novel Pathogenic Variants in a French Cohort Widen the Mutational Spectrum of GNE Myopathy. Journal of Neuromuscular Diseases. 2(2). 131–136. 8 indexed citations
14.
Blandin, Gaëlle, Christophe Béroud, Véronique Labelle, et al.. (2011). UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene. Human Mutation. 33(3). E2317–E2331. 36 indexed citations
15.
Mellgren, Ronald L., Katsuya Miyake, Irina Kramerova, et al.. (2009). Calcium-dependent plasma membrane repair requires m- or μ-calpain, but not calpain-3, the proteasome, or caspases. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(12). 1886–1893. 61 indexed citations
16.
Wein, Nicolas, Marc Bartoli, Cyriaque Beley, et al.. (2009). Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping. Human Mutation. 31(2). 136–142. 62 indexed citations
17.
Wein, Nicolas, Marc Bartoli, Karine Nguyen, et al.. (2009). Immunolabelling and flow cytometry as new tools to explore dysferlinopathies. Neuromuscular Disorders. 20(1). 57–60. 12 indexed citations
18.
Bartoli, Marc, Evelyne Gicquel, Marie Malissen, et al.. (2008). Mannosidase I inhibition rescues the human α-sarcoglycan R77C recurrent mutation. Human Molecular Genetics. 17(9). 1214–1221. 52 indexed citations
19.
Danièle, Nathalie, et al.. (2007). Ins and outs of therapy in limb girdle muscular dystrophies. The International Journal of Biochemistry & Cell Biology. 39(9). 1608–1624. 30 indexed citations
20.
Bartoli, Marc & Isabelle Richard. (2005). Calpains in muscle wasting. The International Journal of Biochemistry & Cell Biology. 37(10). 2115–2133. 142 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

Breakdown of academic impact, for papers by Motoi Kanagawa Breakdown of academic impact, for papers by Svetlana Bezprozvannaya Breakdown of academic impact, for papers by Elizabeth Vafiadaki Breakdown of academic impact, for papers by E. Bonilla Breakdown of academic impact, for papers by Louise V.B. Anderson Breakdown of academic impact, for papers by Stephen J. Crocker Breakdown of academic impact, for papers by F S Walsh Breakdown of academic impact, for papers by Xin‐Ming Shen Breakdown of academic impact, for papers by Martine Pinçon‐Raymond Breakdown of academic impact, for papers by Karl J. A. McCullagh
Rankless by CCL
2026