Marc Bitoun

9.3k total citations
64 papers, 2.1k citations indexed

About

Marc Bitoun is a scholar working on Cell Biology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marc Bitoun has authored 64 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Cell Biology, 40 papers in Molecular Biology and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marc Bitoun's work include Cellular transport and secretion (31 papers), Muscle Physiology and Disorders (16 papers) and Genetic Neurodegenerative Diseases (15 papers). Marc Bitoun is often cited by papers focused on Cellular transport and secretion (31 papers), Muscle Physiology and Disorders (16 papers) and Genetic Neurodegenerative Diseases (15 papers). Marc Bitoun collaborates with scholars based in France, United States and United Kingdom. Marc Bitoun's co-authors include Pascale Guicheney, Marcel Tappaz, Bernard Prudhon, Norma B. Romero, Anne‐Cécile Durieux, Michel Fardeau, B. Eymard, Jocelyn Laporte, Jorge A. Bevilacqua and Stéphane Vassilopoulos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Marc Bitoun

60 papers receiving 2.1k 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 Bitoun France 29 1.3k 1.1k 519 435 278 64 2.1k
Andreas Roos Germany 25 1.3k 0.9× 492 0.4× 501 1.0× 195 0.4× 187 0.7× 134 2.1k
Karin Schwarz Germany 21 1.3k 1.0× 425 0.4× 452 0.9× 117 0.3× 215 0.8× 45 2.9k
C. Jimenez‐Mallebrera Spain 25 1.5k 1.1× 303 0.3× 256 0.5× 273 0.6× 207 0.7× 78 1.9k
Angela Huebner Germany 33 1.7k 1.3× 603 0.5× 324 0.6× 380 0.9× 180 0.6× 133 3.4k
Rita Barresi United Kingdom 19 1.8k 1.4× 497 0.5× 451 0.9× 542 1.2× 352 1.3× 36 2.1k
Montse Olivé Spain 30 1.5k 1.1× 466 0.4× 634 1.2× 693 1.6× 178 0.6× 106 2.2k
Anna Fidziańska Poland 25 1.8k 1.3× 347 0.3× 382 0.7× 802 1.8× 122 0.4× 121 2.3k
Weichun Lin United States 24 1.7k 1.3× 685 0.6× 1.1k 2.2× 134 0.3× 183 0.7× 46 2.5k
Cecı́lia Conde Argentina 15 1.2k 0.9× 776 0.7× 594 1.1× 127 0.3× 179 0.6× 28 1.9k
F S Walsh United Kingdom 32 1.8k 1.4× 403 0.4× 809 1.6× 204 0.5× 297 1.1× 56 2.8k

Countries citing papers authored by Marc Bitoun

Since Specialization
Citations

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

Fields of papers citing papers by Marc Bitoun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Bitoun

This figure shows the co-authorship network connecting the top 25 collaborators of Marc Bitoun. A scholar is included among the top collaborators of Marc Bitoun 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 Bitoun. Marc Bitoun 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.
Pinzón, Natalia, et al.. (2025). Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome. The American Journal of Human Genetics. 112(10). 2440–2457.
2.
Palmero, María José Guerra, Jorge A. Bevilacqua, Ana M. Cárdenas, et al.. (2023). A centronuclear myopathy‐causing mutation in dynamin‐2 disrupts neuronal morphology and excitatory synaptic transmission in a murine model of the disease. Neuropathology and Applied Neurobiology. 49(4). e12918–e12918. 3 indexed citations
3.
Lainé, Jeanne, Marion Benoist, Gilles Moulay, et al.. (2023). Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation. eLife. 12. 13 indexed citations
4.
Trochet, Delphine, Bernard Prudhon, Maud Beuvin, et al.. (2022). Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy. Molecular Therapy — Nucleic Acids. 27. 1179–1190. 2 indexed citations
5.
Peccate, Cécile, Anne Forand, Laura Julien, et al.. (2022). Muscle regeneration affects Adeno Associated Virus 1 mediated transgene transcription. Scientific Reports. 12(1). 9674–9674. 8 indexed citations
6.
Trochet, Delphine & Marc Bitoun. (2021). A review of Dynamin 2 involvement in cancers highlights a promising therapeutic target. Journal of Experimental & Clinical Cancer Research. 40(1). 238–238. 27 indexed citations
7.
Moulay, Gilles, Jeanne Lainé, Masayuki Nakamori, et al.. (2020). Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques. The Journal of Cell Biology. 219(9). 34 indexed citations
8.
Lainé, Jeanne, et al.. (2019). Revealing alternative splicing control of clathrin structural plasticity in health and disease. SPIRE - Sciences Po Institutional REpository.
9.
Lainé, Jeanne, Gilles Moulay, Michaël Trichet, et al.. (2019). Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle. Molecular Biology of the Cell. 30(5). 579–590. 36 indexed citations
10.
Szentesi, Péter, Bruno Allard, Delphine Trochet, et al.. (2017). Impaired excitation–contraction coupling in muscle fibres from the dynamin2R465W mouse model of centronuclear myopathy. The Journal of Physiology. 595(24). 7369–7382. 19 indexed citations
11.
Azibani, Fériel, Astrid Brull, Ludovic Arandel, et al.. (2017). Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy. Molecular Therapy — Nucleic Acids. 10. 376–386. 32 indexed citations
12.
González‐Jamett, Arlek M., María José Guerra Palmero, Mai Thao Bui, et al.. (2017). Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells. Scientific Reports. 7(1). 28 indexed citations
13.
Durieux, Anne‐Cécile, Stéphane Vassilopoulos, Jeanne Lainé, et al.. (2012). A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice. Traffic. 13(6). 869–879. 44 indexed citations
14.
McClelland, Verity M., Thomas Cullup, István Bódi, et al.. (2010). Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy. American Journal of Medical Genetics Part A. 152A(3). 741–747. 35 indexed citations
15.
Bevilacqua, Jorge A., Nicole Monnier, Marc Bitoun, et al.. (2010). Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. Neuropathology and Applied Neurobiology. 37(3). 271–284. 75 indexed citations
16.
Bitoun, Marc, Anne‐Cécile Durieux, Bernard Prudhon, et al.. (2009). Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis. Human Mutation. 30(10). 1419–1427. 67 indexed citations
17.
Dubrovsky, Alberto, et al.. (2007). C.P.4.11 Ragged red fibres finding in muscle biopsy of dynamin 2-related centronuclear myopathy. Neuromuscular Disorders. 17(9-10). 881–882. 2 indexed citations
18.
Bitoun, Marc, Jorge A. Bevilacqua, Bernard Prudhon, et al.. (2007). Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset. Annals of Neurology. 62(6). 666–670. 104 indexed citations
19.
Cifuentes-Díaz, Carmen, Marc Bitoun, Danièle Goudou, et al.. (2003). Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin. Muscle & Nerve. 29(1). 59–65. 13 indexed citations
20.
Tappaz, Marcel, Marc Bitoun, Isabelle Reymond, & Alain Sergeant. (1999). Characterization of the cDNA Coding for Rat Brain Cysteine Sulfinate Decarboxylase. Journal of Neurochemistry. 73(3). 903–912. 21 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 Andreas Roos Breakdown of academic impact, for papers by Karin Schwarz Breakdown of academic impact, for papers by C. Jimenez‐Mallebrera Breakdown of academic impact, for papers by Angela Huebner Breakdown of academic impact, for papers by Rita Barresi Breakdown of academic impact, for papers by Montse Olivé Breakdown of academic impact, for papers by Anna Fidziańska Breakdown of academic impact, for papers by Weichun Lin Breakdown of academic impact, for papers by Cecı́lia Conde Breakdown of academic impact, for papers by F S Walsh
Rankless by CCL
2026