Vincent Gache

1.8k total citations
39 papers, 1.2k citations indexed

About

Vincent Gache is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Vincent Gache has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 17 papers in Cell Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Vincent Gache's work include Nuclear Structure and Function (11 papers), Muscle Physiology and Disorders (9 papers) and Microtubule and mitosis dynamics (8 papers). Vincent Gache is often cited by papers focused on Nuclear Structure and Function (11 papers), Muscle Physiology and Disorders (9 papers) and Microtubule and mitosis dynamics (8 papers). Vincent Gache collaborates with scholars based in France, Germany and Portugal. Vincent Gache's co-authors include Edgar R. Gomes, Bruno Cadot, Mary K. Baylies, Brian E. Richardson, Eric S. Folker, Sestina Falcone, Didier Job, Anne Fourest‐Lieuvin, Leticia Peris and Violaine Lantez and has published in prestigious journals such as Nature, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Vincent Gache

36 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Gache France 16 892 446 137 134 95 39 1.2k
Eric S. Folker United States 18 1.4k 1.6× 860 1.9× 139 1.0× 151 1.1× 125 1.3× 32 1.7k
Manolis Mavroidis Greece 21 937 1.1× 472 1.1× 159 1.2× 336 2.5× 128 1.3× 44 1.4k
Ling T. Guo United States 19 880 1.0× 258 0.6× 118 0.9× 130 1.0× 114 1.2× 74 1.2k
Iakowos Karakesisoglou Germany 25 1.9k 2.2× 1.1k 2.5× 105 0.8× 86 0.6× 127 1.3× 39 2.6k
Ryan Schreiner United States 22 847 0.9× 588 1.3× 134 1.0× 32 0.2× 204 2.1× 43 1.5k
Tatiana V. Cohen United States 16 1.4k 1.6× 164 0.4× 80 0.6× 66 0.5× 196 2.1× 21 1.6k
Steven C. Miller United States 11 1.2k 1.3× 201 0.5× 76 0.6× 64 0.5× 96 1.0× 19 1.5k
Ewa Dziak Canada 15 671 0.8× 551 1.2× 93 0.7× 86 0.6× 45 0.5× 25 1.2k
Roberta Sacchetto Italy 19 623 0.7× 124 0.3× 227 1.7× 183 1.4× 82 0.9× 59 888
Angela Lek United States 14 686 0.8× 169 0.4× 59 0.4× 108 0.8× 128 1.3× 24 813

Countries citing papers authored by Vincent Gache

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Gache

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Gache

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Gache. A scholar is included among the top collaborators of Vincent Gache 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 Vincent Gache. Vincent Gache 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.
Streichenberger, Nathalie, et al.. (2025). Interplay between microtubule interactome, myonuclei mechanotransduction, and positioning in myopathies. Nucleus. 16(1). 2524909–2524909.
2.
Abitbol, Marie, et al.. (2024). Different Founding Effects Underlie Dominant Blue Eyes (DBE) in the Domestic Cat. Animals. 14(13). 1845–1845. 1 indexed citations
3.
4.
Grosjean, Isabelle, et al.. (2023). Human Induced Pluripotent Spheroids’ Growth Is Driven by Viscoelastic Properties and Macrostructure of 3D Hydrogel Environment. Bioengineering. 10(12). 1418–1418. 6 indexed citations
5.
Schaeffer, Laurent, et al.. (2022). Simple Methods for Permanent or Transient Denervation in Mouse Sciatic Nerve Injury Models. BIO-PROTOCOL. 12(11). 1 indexed citations
6.
Abitbol, Marie, Valérie Risson, Emmanuelle Girard, et al.. (2021). MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis. eLife. 10. 10 indexed citations
7.
Prokic, Ivana, Belinda S. Cowling, Christine Kretz, et al.. (2020). Differential physiological roles for BIN1 isoforms in skeletal muscle development, function and regeneration. Disease Models & Mechanisms. 13(11). 25 indexed citations
8.
Ravel‐Chapuis, Aymeric, et al.. (2020). HDAC6 regulates microtubule stability and clustering of AChRs at neuromuscular junctions. The Journal of Cell Biology. 219(8). 34 indexed citations
9.
Janin, Alexandre, Francesca Ratti, A. Bertrand, et al.. (2018). SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells. Scientific Reports. 8(1). 5618–5618. 5 indexed citations
10.
Richard, Magali, Christian Stigloher, Vincent Gache, et al.. (2018). CRELD1 is an evolutionarily-conserved maturational enhancer of ionotropic acetylcholine receptors. eLife. 7. 15 indexed citations
11.
Janin, Alexandre & Vincent Gache. (2018). Nesprins and Lamins in Health and Diseases of Cardiac and Skeletal Muscles. Frontiers in Physiology. 9. 1277–1277. 35 indexed citations
12.
Gache, Vincent, Edgar R. Gomes, & Bruno Cadot. (2017). Microtubule motors involved in nuclear movement during skeletal muscle differentiation. Molecular Biology of the Cell. 28(7). 865–874. 36 indexed citations
13.
Vernochet, Cécile, Virginie Mariot, Vincent Gache, et al.. (2016). Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice. PLoS Genetics. 12(9). e1006289–e1006289. 38 indexed citations
14.
Hnia, Karim, Vincent Gache, Catherine Koch, et al.. (2015). Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton. Developmental Cell. 35(2). 186–198. 55 indexed citations
15.
Falcone, Sestina, William Roman, Karim Hnia, et al.. (2014). N‐ WASP is required for Amphiphysin‐2/ BIN 1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy. EMBO Molecular Medicine. 6(11). 1455–1475. 85 indexed citations
16.
Gache, Vincent, Bruno Cadot, Eric S. Folker, et al.. (2012). MAP and kinesin-dependent nuclear positioning is required for skeletal muscle function. Nature. 484(7392). 120–124. 208 indexed citations
17.
Bigot, Anne, Søren Skov Jensen, Jayne L. Dennis, et al.. (2012). In-depth analysis of the secretome identifies three major independent secretory pathways in differentiating human myoblasts. Journal of Proteomics. 77. 344–356. 122 indexed citations
18.
Gache, Vincent, Patrice Waridel, Christof Winter, et al.. (2010). Xenopus Meiotic Microtubule-Associated Interactome. PLoS ONE. 5(2). e9248–e9248. 37 indexed citations
19.
Fourest‐Lieuvin, Anne, Leticia Peris, Vincent Gache, et al.. (2005). Microtubule Regulation in Mitosis: Tubulin Phosphorylation by the Cyclin-dependent Kinase Cdk1. Molecular Biology of the Cell. 17(3). 1041–1050. 150 indexed citations
20.
Gache, Vincent, et al.. (2004). Identification of proteins binding the native tubulin dimer. Biochemical and Biophysical Research Communications. 327(1). 35–42. 23 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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