Guillaume Bassez

6.9k total citations · 1 hit paper
93 papers, 3.5k citations indexed

About

Guillaume Bassez is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Guillaume Bassez has authored 93 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 51 papers in Cellular and Molecular Neuroscience and 35 papers in Neurology. Recurrent topics in Guillaume Bassez's work include Genetic Neurodegenerative Diseases (49 papers), Muscle Physiology and Disorders (24 papers) and Mitochondrial Function and Pathology (20 papers). Guillaume Bassez is often cited by papers focused on Genetic Neurodegenerative Diseases (49 papers), Muscle Physiology and Disorders (24 papers) and Mitochondrial Function and Pathology (20 papers). Guillaume Bassez collaborates with scholars based in France, United States and Netherlands. Guillaume Bassez's co-authors include Romain K. Gherardi, François‐Jérôme Authier, B. Eymard, Bénédicte Chazaud, Pascal Laforêt, Christo Christov, Shahragim Tajbakhsh, Vasily Shinin, Fabrice Chrétien and Rana Abou-Khalil and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Guillaume Bassez

85 papers receiving 3.5k citations

Hit Papers

Muscle Satellite Cells and Endothelial Cells: Close Neigh... 2007 2026 2013 2019 2007 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guillaume Bassez France 33 2.5k 1.4k 672 475 424 93 3.5k
Lucía Morandi Italy 43 3.7k 1.5× 754 0.5× 490 0.7× 835 1.8× 786 1.9× 143 5.2k
Pia Bernasconi Italy 39 1.7k 0.7× 525 0.4× 1.5k 2.2× 460 1.0× 288 0.7× 111 3.9k
J. T. Kissel United States 28 1.1k 0.4× 817 0.6× 1.0k 1.6× 353 0.7× 235 0.6× 50 2.8k
Antje Bornemann Germany 28 1.5k 0.6× 624 0.4× 850 1.3× 529 1.1× 126 0.3× 88 3.3k
Beril Talim Türkiye 31 3.0k 1.2× 580 0.4× 175 0.3× 487 1.0× 492 1.2× 138 4.0k
Reginald E. Bittner Austria 34 2.1k 0.8× 417 0.3× 233 0.3× 411 0.9× 509 1.2× 82 3.5k
Sinem Karaman Switzerland 26 1.2k 0.5× 1.2k 0.9× 655 1.0× 216 0.5× 141 0.3× 43 4.5k
F.M.S. Tomé France 32 3.9k 1.6× 1.5k 1.1× 214 0.3× 607 1.3× 707 1.7× 72 4.4k
Morten Dunø Denmark 35 2.6k 1.0× 745 0.5× 346 0.5× 281 0.6× 481 1.1× 184 3.8k
Patrizia Sabatelli Italy 39 4.3k 1.7× 478 0.3× 176 0.3× 539 1.1× 553 1.3× 147 5.6k

Countries citing papers authored by Guillaume Bassez

Since Specialization
Citations

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

Fields of papers citing papers by Guillaume Bassez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guillaume Bassez

This figure shows the co-authorship network connecting the top 25 collaborators of Guillaume Bassez. A scholar is included among the top collaborators of Guillaume Bassez 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 Guillaume Bassez. Guillaume Bassez 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.
Benvéniste, Olivier, et al.. (2025). Key determinants of impaired gait performance in adults with neuromuscular diseases: a multiparametric and multimodal analysis. Journal of Applied Physiology. 138(5). 1261–1274.
2.
Benarroch, Louise, Pierre‐Yves Boëlle, Nobuyuki Eura, et al.. (2025). Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion Disorders. Genomics Proteomics & Bioinformatics.
3.
Tsai, Yu‐Chih, Cheryl Heiner, Tanya Stojkovic, et al.. (2022). Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing. Journal of Molecular Diagnostics. 24(11). 1143–1154. 13 indexed citations
4.
Fayssoil, Abdallah, Tanya Stojkovic, Adam Ogna, et al.. (2019). Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy. Medicine. 98(4). e13887–e13887. 3 indexed citations
5.
Sellier, Chantal, Estefanía Cerro-Herreros, Markus Blatter, et al.. (2018). rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. Nature Communications. 9(1). 2009–2009. 57 indexed citations
6.
Jauvin, Dominic, Sanjay K. Pandey, Guillaume Bassez, et al.. (2017). Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice. Molecular Therapy — Nucleic Acids. 7. 465–474. 63 indexed citations
7.
Chong-Nguyen, C., Karim Wahbi, Vincent Algalarrondo, et al.. (2017). Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1. Circulation Cardiovascular Genetics. 10(3). 32 indexed citations
8.
Antonio, Marie De, et al.. (2016). Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification. Revue Neurologique. 172(10). 572–580. 167 indexed citations
9.
Wahbi, Karim, F. Sébag, Nicolas Lellouche, et al.. (2016). Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome. Neuromuscular Disorders. 26(3). 227–233. 13 indexed citations
10.
Beller, Christine Le, Pierre Boutouyrie, Guillaume Bassez, et al.. (2013). Distinctive clinical features in arthro-myalgic patients with and without aluminum hydroxyde-induced macrophagic myofasciitis: An exploratory study. Journal of Inorganic Biochemistry. 128. 262–266. 9 indexed citations
11.
Laforêt, Pascal, Tanya Stojkovic, Guillaume Bassez, et al.. (2012). Neutral lipid storage disease with myopathy: A whole-body nuclear MRI and metabolic study. Molecular Genetics and Metabolism. 108(2). 125–131. 26 indexed citations
12.
Udd, Bjarne, G. Meola, Ralf Krahe, et al.. (2011). Myotonic dystrophy type 2 (DM2) and related disorders. Neuromuscular Disorders. 21(6). 443–450. 37 indexed citations
13.
Furby, A., Anthony Béhin, Katell Beauvais, et al.. (2009). Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series. Journal of Neurology Neurosurgery & Psychiatry. 81(1). 101–104. 51 indexed citations
14.
Wahbi, Karim, Christophe Meune, Henri Marc Bécane, et al.. (2009). Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: A case control study. Neuromuscular Disorders. 19(7). 468–472. 46 indexed citations
15.
Boërio, Delphine, Jean‐Yves Hogrel, Guillaume Bassez, & Jean-Pascal Lefaucheur. (2007). Neuromuscular excitability properties in myotonic dystrophy type 1. Clinical Neurophysiology. 118(11). 2375–2382. 7 indexed citations
16.
Christov, Christo, Fabrice Chrétien, Rana Abou-Khalil, et al.. (2007). Muscle Satellite Cells and Endothelial Cells: Close Neighbors and Privileged Partners. Molecular Biology of the Cell. 18(4). 1397–1409. 512 indexed citations breakdown →
17.
Nguyen, Karine, Guillaume Bassez, Martin Krahn, et al.. (2007). Phenotypic Study in 40 Patients With Dysferlin Gene Mutations. Archives of Neurology. 64(8). 1176–1176. 184 indexed citations
18.
Charniot, Jean‐Christophe, Michel Desnos, Dominique Bonnefont‐Rousselot, et al.. (2005). Severe Dilated Cardiomyopathy and Quadriceps Myopathy Due to Lamin A/C Gene Mutation: A Phenotypic Study. European Journal of Heart Failure. 8(3). 249–256. 22 indexed citations
19.
Bassez, Guillaume, Arnaud Lazarus, Isabelle Desguerre, et al.. (2004). Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1. Neurology. 63(10). 1939–1941. 73 indexed citations
20.
Bassez, Guillaume, C. Kaplan, D. Vauthier-Brouzes, & Martin Catala. (2001). A case of antenatal cerebral haemorrhage resulting from maternal alloimmunisation against fetal platelets. Child s Nervous System. 17(4-5). 302–304. 3 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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