Isabelle Marty

4.8k total citations
106 papers, 3.5k citations indexed

About

Isabelle Marty is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Isabelle Marty has authored 106 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 34 papers in Cardiology and Cardiovascular Medicine and 27 papers in Cellular and Molecular Neuroscience. Recurrent topics in Isabelle Marty's work include Ion channel regulation and function (46 papers), Muscle Physiology and Disorders (27 papers) and Cardiomyopathy and Myosin Studies (20 papers). Isabelle Marty is often cited by papers focused on Ion channel regulation and function (46 papers), Muscle Physiology and Disorders (27 papers) and Cardiomyopathy and Myosin Studies (20 papers). Isabelle Marty collaborates with scholars based in France, United States and Italy. Isabelle Marty's co-authors include Michel Villaz, Yves Meyer, Joël Lunardi, Julien Fauré, Michel Ronjat, Julie Brocard, Jane‐Lise Samuel, Christophe Heymes, Yvette Chartier and Nicole Monnier and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Isabelle Marty

99 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabelle Marty France 36 2.8k 1.3k 643 509 466 106 3.5k
Geert Callewaert Belgium 39 2.5k 0.9× 702 0.5× 1.1k 1.8× 388 0.8× 669 1.4× 90 4.1k
Jianjie Ma United States 43 4.5k 1.6× 1.9k 1.4× 1.7k 2.7× 632 1.2× 686 1.5× 97 5.5k
Peter Vangheluwe Belgium 34 1.9k 0.7× 555 0.4× 381 0.6× 531 1.0× 590 1.3× 86 3.2k
Anna Raffaello Italy 26 5.0k 1.8× 315 0.2× 1.1k 1.8× 1.1k 2.2× 788 1.7× 44 6.1k
Leo J. Pallanck United States 35 3.9k 1.4× 337 0.3× 2.0k 3.1× 1.0k 2.0× 867 1.9× 63 6.3k
Serge Arnaudeau Switzerland 24 1.6k 0.6× 231 0.2× 549 0.9× 362 0.7× 491 1.1× 30 2.4k
Alfredo Margreth Italy 32 2.0k 0.7× 647 0.5× 544 0.8× 353 0.7× 520 1.1× 91 2.5k
Dong Wook Shin South Korea 27 1.0k 0.4× 209 0.2× 522 0.8× 285 0.6× 382 0.8× 76 2.5k
David C. Johns United States 37 2.5k 0.9× 1.5k 1.1× 865 1.3× 321 0.6× 194 0.4× 65 3.6k
Forrest Fuller United States 20 1.7k 0.6× 445 0.3× 448 0.7× 1.1k 2.2× 204 0.4× 23 3.0k

Countries citing papers authored by Isabelle Marty

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Marty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Marty

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Marty. A scholar is included among the top collaborators of Isabelle Marty 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 Isabelle Marty. Isabelle Marty 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.
Benstaali, Caroline, Julie Brocard, Benoı̂t Giannesini, et al.. (2025). Limited pre-clinical relevance of the heterozygous RYR1-I4895T/+ mouse model due to its mild phenotype. Journal of Neuromuscular Diseases. 708646490–708646490.
2.
Brocard, Julie, Kamel Mamchaoui, Norma B. Romero, et al.. (2024). Functional benefit of CRISPR-Cas9-induced allele deletion for RYR1 dominant mutation. Molecular Therapy — Nucleic Acids. 35(3). 102259–102259. 1 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.
Marty, Isabelle, et al.. (2022). Gene therapies for RyR1-related myopathies. Current Opinion in Pharmacology. 68. 102330–102330. 2 indexed citations
5.
Chivet, Mathilde, Anne‐Sophie Nicot, Julie Brocard, et al.. (2022). Huntingtin regulates calcium fluxes in skeletal muscle. The Journal of General Physiology. 155(1). 7 indexed citations
6.
Rendu, John, et al.. (2021). Therapies for RYR1-Related Myopathies: Where We Stand and the Perspectives. Current Pharmaceutical Design. 28(1). 15–25. 8 indexed citations
7.
Luo, Shiyu, Qifei Li, Jasmine Lin, et al.. (2020). SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins. Human Molecular Genetics. 29(24). 3882–3891. 7 indexed citations
8.
Pelletier, Laurent, Anne Petiot, Julie Brocard, et al.. (2020). In vivo RyR1 reduction in muscle triggers a core-like myopathy. Acta Neuropathologica Communications. 8(1). 192–192. 15 indexed citations
9.
Cacheux, Marine, Jérémy Fauconnier, Jérôme Thireau, et al.. (2019). Interplay between Triadin and Calsequestrin in the Pathogenesis of CPVT in the Mouse. Molecular Therapy. 28(1). 171–179. 20 indexed citations
10.
Giannesini, Benoı̂t, Julie Brocard, Mathilde Chivet, et al.. (2018). Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction. Skeletal Muscle. 8(1). 30–30. 19 indexed citations
11.
Jungbluth, Heinz, James J. Dowling, Ana Ferreiro, et al.. (2016). 217th ENMC International Workshop: RYR1-related myopathies, Naarden, The Netherlands, 29–31 January 2016. Neuromuscular Disorders. 26(9). 624–633. 32 indexed citations
12.
Baudet, Mathieu, et al.. (2016). Triadin and CLIMP-63 form a link between triads and microtubules in muscle cells. Journal of Cell Science. 129(20). 3744–3755. 25 indexed citations
13.
Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations
14.
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
15.
Fauré, Julien, et al.. (2009). Triadin Function In Sarcoplasmic Reticulum Structure?. Biophysical Journal. 96(3). 237a–237a. 1 indexed citations
16.
Oddoux, Sarah, Julie Brocard, Annie Schweitzer, et al.. (2009). Triadin Deletion Induces Impaired Skeletal Muscle Function. Journal of Biological Chemistry. 284(50). 34918–34929. 71 indexed citations
17.
Monnier, Nicole, et al.. (2007). C.P.1.05 Congenital fibre type disproportion associated with de novo mutations in TPM3 and ACTA1 genes. Neuromuscular Disorders. 17(9-10). 835–835. 1 indexed citations
18.
Jouk, Pierre‐Simon, Annick Labarre‐Vila, Paulette Mezin, et al.. (2007). C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia. Neuromuscular Disorders. 17(9-10). 837–838. 2 indexed citations
19.
Goonasekera, Sanjeewa A., Nicole A. Beard, Linda Groom, et al.. (2007). Triadin Binding to the C-Terminal Luminal Loop of the Ryanodine Receptor is Important for Skeletal Muscle Excitation–Contraction Coupling. The Journal of General Physiology. 130(4). 365–378. 65 indexed citations
20.
Marty, Isabelle, et al.. (1993). Growth-related gene expression in Nicotiana tabacum mesophyll protoplasts. HAL (Le Centre pour la Communication Scientifique Directe). 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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