J. Cuisset

1.3k total citations
21 papers, 157 citations indexed

About

J. Cuisset is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, J. Cuisset has authored 21 papers receiving a total of 157 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in J. Cuisset's work include Neurogenetic and Muscular Disorders Research (9 papers), Muscle Physiology and Disorders (8 papers) and Cardiomyopathy and Myosin Studies (4 papers). J. Cuisset is often cited by papers focused on Neurogenetic and Muscular Disorders Research (9 papers), Muscle Physiology and Disorders (8 papers) and Cardiomyopathy and Myosin Studies (4 papers). J. Cuisset collaborates with scholars based in France, Switzerland and Belgium. J. Cuisset's co-authors include B. Estournet, Louis Vallée, Stéphane Auvin, Claude Alain Maurage, Francis Leclerc, François Rivier, Louise Devisme, Gustavo Soto‐Ares, D. Guimber and V. Tiffreau and has published in prestigious journals such as Clinical Nutrition, Neuromuscular Disorders and Seizure.

In The Last Decade

J. Cuisset

21 papers receiving 151 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Cuisset France 7 81 52 34 24 20 21 157
Marjorie Illingworth United Kingdom 5 142 1.8× 93 1.8× 28 0.8× 65 2.7× 12 0.6× 8 239
Caroline Espil‐Taris France 10 113 1.4× 31 0.6× 10 0.3× 35 1.5× 7 0.3× 20 211
Matthew Harmelink United States 6 37 0.5× 20 0.4× 25 0.7× 15 0.6× 16 0.8× 12 99
Ling Jun Huan Canada 7 101 1.2× 15 0.3× 22 0.6× 8 0.3× 10 0.5× 8 261
R. Kulshrestha United Kingdom 8 151 1.9× 30 0.6× 16 0.5× 33 1.4× 15 0.8× 25 258
Acary Sousa Bulle Oliveira Brazil 8 40 0.5× 27 0.5× 18 0.5× 27 1.1× 4 0.2× 14 161
Sasha Živković United States 6 46 0.6× 17 0.3× 13 0.4× 15 0.6× 9 0.5× 9 113
Emily J. Todd United States 4 42 0.5× 27 0.5× 10 0.3× 29 1.2× 7 0.3× 5 108
Erik Andersen Australia 7 86 1.1× 13 0.3× 7 0.2× 15 0.6× 21 1.1× 22 213
Fumihito Nozaki Japan 8 85 1.0× 5 0.1× 16 0.5× 34 1.4× 17 0.8× 24 195

Countries citing papers authored by J. Cuisset

Since Specialization
Citations

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

Fields of papers citing papers by J. Cuisset

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Cuisset

This figure shows the co-authorship network connecting the top 25 collaborators of J. Cuisset. A scholar is included among the top collaborators of J. Cuisset 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 J. Cuisset. J. Cuisset 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.
Seferian, A., A. Moraux, Teresa Gidaro, et al.. (2017). Innovative home activity monitoring in non-ambulant patients with spinal muscular atrophy: a multicenter observational trial. Neuromuscular Disorders. 27. S225–S225. 1 indexed citations
2.
Chabanon, A., M. Annoussamy, Aurore Daron, et al.. (2017). Longitudinal data of the European prospective natural history study of patients with type 2 and 3 spinal muscular atrophy. Neuromuscular Disorders. 27. S134–S134. 3 indexed citations
3.
Muntoni, Francesco, Beatrice Berti, Éric Dessaud, et al.. (2017). Olesoxime in patients with type 2 or non-ambulatory type 3 Spinal muscular atrophy: a placebo-controlled phase 2 trial including a long-term, open-label follow-up study. Neuromuscular Disorders. 27. S209–S210. 1 indexed citations
4.
Buyse, Gunnar, Thomas Voït, Ulrike Schara, et al.. (2016). Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy. Neuromuscular Disorders. 26. S156–S157. 1 indexed citations
5.
Chabanon, A., Yann Péréon, Aurore Daron, et al.. (2016). Baseline data from a European prospective and longitudinal natural history study of patients with type 2 and 3 spinal muscular atrophy – NatHis-SMA. Neuromuscular Disorders. 26. S103–S103. 2 indexed citations
6.
Annoussamy, M., C. Lilien, Teresa Gidaro, et al.. (2016). Baseline data from patients with myotubular myopathy enrolled in a European prospective and longitudinal natural history study. Neuromuscular Disorders. 26. S116–S117. 1 indexed citations
7.
Cuisset, J. & François Rivier. (2015). Manifestations centrales des dystrophinopathies. Archives de Pédiatrie. 22(12). 12S58–12S62. 3 indexed citations
8.
Annoussamy, M., C. Lilien, G. Ollivier, et al.. (2015). Natural history and functional status of patients with myotubular myopathy enrolled in a prospective and longitudinal study. Neuromuscular Disorders. 25. S274–S274. 1 indexed citations
9.
Meier, Thomas, Christian Rummey, M. Leinonen, et al.. (2015). The use of a hand-held device (ASMA-1) for home-based monitoring of respiratory function changes in pediatric and adolescent patients with Duchenne muscular dystrophy. Neuromuscular Disorders. 25. S201–S201. 2 indexed citations
10.
LeMeur, Marianne, Carole Vuillerot, V. Tiffreau, et al.. (2015). Changes in muscle activation during gait of children with duchenne muscular dystrophy. Computer Methods in Biomechanics & Biomedical Engineering. 18(sup1). 2042–2043. 2 indexed citations
11.
Barnérias, Christine, Sandra Quijano, M. Mayer, et al.. (2014). Amyotrophie spinale type 1 : enquête multicentrique des pratiques de soins et d’accompagnement palliatif sur deux périodes successives de 10ans. Archives de Pédiatrie. 21(4). 347–354. 7 indexed citations
12.
Cuisset, J., et al.. (2013). Intérêt de la biopsie musculaire chez l’enfant en 2012. Revue Neurologique. 169(8-9). 632–639. 5 indexed citations
13.
Cuisset, J. & B. Estournet. (2012). Recommendations for the diagnosis and management of typical childhood spinal muscular atrophy. Revue Neurologique. 168(12). 902–909. 13 indexed citations
14.
Séguy, D., N. Pellegrini, David Orlikowski, et al.. (2009). Efficacy and tolerance of gastrostomy feeding in Duchenne muscular dystrophy. Clinical Nutrition. 29(1). 60–64. 24 indexed citations
15.
Sabouraud, Pascal, J. Cuisset, C. Cancès, et al.. (2009). Stratégie diagnostique devant une hyperCKémie chez l’enfant. Archives de Pédiatrie. 16(6). 678–680. 2 indexed citations
16.
Carmignac, Virginie, Sarika Sharma, Sandrine Arbogast, et al.. (2009). G.O.7 A homozygous desmin deletion causes an Emery-Dreifuss like recessive myopathy with desmin depletion. Neuromuscular Disorders. 19(8-9). 600–600. 16 indexed citations
17.
Auvin, Stéphane, Louise Devisme, Claude Alain Maurage, et al.. (2007). Neuropathological and MRI findings in an acute presentation of hemiconvulsion-hemiplegia: A report with pathophysiological implications. Seizure. 16(4). 371–376. 25 indexed citations
18.
Cuisset, J., et al.. (2005). Troubles psychiatriques révélateurs d’une maladie de Niemann-Pick de type C à l’âge adulte. Revue Neurologique. 161(3). 318–322. 9 indexed citations
19.
Tuffery‐Giraud, Sylvie, Bernard Échenne, J. Cuisset, et al.. (2004). The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre. Neuromuscular Disorders. 14(10). 650–658. 34 indexed citations
20.
Cuisset, J., et al.. (2000). Cas radiologique du mois. Archives de Pédiatrie. 7(1). 75–77. 4 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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