B. Estournet

5.5k total citations
72 papers, 2.9k citations indexed

About

B. Estournet is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, B. Estournet has authored 72 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 23 papers in Genetics and 13 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in B. Estournet's work include Muscle Physiology and Disorders (28 papers), Neurogenetic and Muscular Disorders Research (22 papers) and Cardiomyopathy and Myosin Studies (13 papers). B. Estournet is often cited by papers focused on Muscle Physiology and Disorders (28 papers), Neurogenetic and Muscular Disorders Research (22 papers) and Cardiomyopathy and Myosin Studies (13 papers). B. Estournet collaborates with scholars based in France, Italy and United Kingdom. B. Estournet's co-authors include Pascale Guicheney, Norma B. Romero, A Barois, Martin Brockington, Thomas Voit, Susana Quijano‐Roy, Ana Ferreiro, Francesco Muntoni, Kevin P. Campbell and A. Leclerc and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

B. Estournet

67 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Estournet France 27 2.2k 706 599 450 375 72 2.9k
Marcello Villanova Italy 27 1.3k 0.6× 223 0.3× 477 0.8× 385 0.9× 217 0.6× 86 2.3k
Adnan Y. Manzur United Kingdom 26 1.5k 0.7× 528 0.7× 535 0.9× 351 0.8× 215 0.6× 63 2.1k
Christopher F. Spurney United States 26 1.3k 0.6× 790 1.1× 149 0.2× 274 0.6× 119 0.3× 80 2.2k
Dalila Laoudj‐Chenivesse France 26 2.1k 0.9× 337 0.5× 447 0.7× 199 0.4× 116 0.3× 54 2.6k
Gunnar Buyse Belgium 28 2.2k 1.0× 578 0.8× 322 0.5× 643 1.4× 238 0.6× 89 3.2k
Hirofumi Komaki Japan 28 1.7k 0.8× 286 0.4× 285 0.5× 363 0.8× 167 0.4× 180 2.5k
Wolfgang Müller‐Felber Germany 31 1.2k 0.6× 209 0.3× 680 1.1× 413 0.9× 341 0.9× 135 3.2k
Shenhav Cohen Israel 16 1.8k 0.8× 327 0.5× 130 0.2× 253 0.6× 623 1.7× 23 2.5k
Teresinha Evangelista Portugal 29 1.2k 0.5× 268 0.4× 741 1.2× 372 0.8× 315 0.8× 103 2.6k
Luisa Politano Italy 31 3.0k 1.4× 1.7k 2.4× 492 0.8× 965 2.1× 386 1.0× 145 4.0k

Countries citing papers authored by B. Estournet

Since Specialization
Citations

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

Fields of papers citing papers by B. Estournet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Estournet

This figure shows the co-authorship network connecting the top 25 collaborators of B. Estournet. A scholar is included among the top collaborators of B. Estournet 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 B. Estournet. B. Estournet 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.
Caggiano, Serena, Sonia Khirani, Ivana Dabaj, et al.. (2017). Diaphragmatic dysfunction in SEPN1-related myopathy. Neuromuscular Disorders. 27(8). 747–755. 30 indexed citations
2.
Catteruccia, Michela, Carole Vuillerot, Isabelle Vaugier, et al.. (2015). Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 Children. Journal of Neuromuscular Diseases. 2(4). 453–462. 21 indexed citations
3.
Eymard, B., Daniel Hantaı̈, & B. Estournet. (2013). Congenital myasthenic syndromes. Handbook of clinical neurology. 113. 1469–1480. 39 indexed citations
4.
Quijano‐Roy, Susana, Sonia Khirani, Marina Colella, et al.. (2013). Diaphragmatic dysfunction in Collagen VI myopathies. Neuromuscular Disorders. 24(2). 125–133. 29 indexed citations
5.
Yaou, Rabah Ben, Claire Navarro, Susana Quijano-Roy, et al.. (2011). Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation. European Journal of Human Genetics. 19(6). 647–654. 36 indexed citations
6.
Abbara, Chadi, B. Estournet, Lucette Lacomblez, et al.. (2010). Riluzole pharmacokinetics in young patients with spinal muscular atrophy. British Journal of Clinical Pharmacology. 71(3). 403–410. 20 indexed citations
7.
Vuillaumier‐Barrot, Sandrine, Susana Quijano-Roy, C. Bouchet-Séraphin, et al.. (2009). Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype. Neuromuscular Disorders. 19(3). 182–188. 30 indexed citations
8.
Allamand, Valérie, Corine Gartioux, Emmanuelle Lacène, et al.. (2007). C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy. Neuromuscular Disorders. 17(9-10). 833–833. 1 indexed citations
9.
Manya, Hiroshi, C Bouchet, Sandrine Vuillaumier‐Barrot, et al.. (2007). Protein O-mannosyltransferase activities in lymphoblasts from patients with α-dystroglycanopathies. Neuromuscular Disorders. 18(1). 45–51. 25 indexed citations
10.
Carmignac, Virginie, Mustafa A. Salih, Susana Quijano‐Roy, et al.. (2007). C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy. Annals of Neurology. 61(4). 340–351. 156 indexed citations
11.
Clarke, Nigel F., Warren Kidson, Susana Quijano‐Roy, et al.. (2006). SEPN1: Associated with congenital fiber‐type disproportion and insulin resistance. Annals of Neurology. 59(3). 546–552. 114 indexed citations
12.
Quijano‐Roy, Susana, Itxaso Martì, S. Makri, et al.. (2005). Brain MRI abnormalities in muscular dystrophy due to FKRP mutations. Brain and Development. 28(4). 232–242. 26 indexed citations
13.
14.
Fauroux, Brigitte, et al.. (2003). Long‐term noninvasive mechanical ventilation for children at home: A national survey. Pediatric Pulmonology. 35(2). 119–125. 93 indexed citations
15.
Mercuri, Eugenio, Martin Brockington, Volker Straub, et al.. (2003). Phenotypic spectrum associated with mutations in the fukutin‐related protein gene. Annals of Neurology. 53(4). 537–542. 172 indexed citations
16.
Quijano‐Roy, Susana, Lucía Galán, Ana Ferreiro, et al.. (2002). Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency. Neuromuscular Disorders. 12(5). 466–475. 20 indexed citations
17.
Ferreiro, Ana, B. Estournet, C Laroche, et al.. (2001). Genetic characterisation of multi-minicore disease: identification of a first locus and evidence for genetic heterogeneity. UCL Discovery (University College London). 1 indexed citations
18.
Chéliout-Héraut, F., Renata Rubinsztajn, Christine Ioos, & B. Estournet. (2001). Prognostic value of evoked potentials and sleep recordings in the prolonged comatose state of children. Preliminary data. Neurophysiologie Clinique. 31(5). 283–292. 32 indexed citations
19.
Carlier, Robert, Jean-Marc Pinard, D. Mompoint, et al.. (1998). Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.. Radiology. 206(3). 811–816. 28 indexed citations
20.
Estournet, B., et al.. (1993). Ondine's Curse: A Discussion of Five Cases. Neuropediatrics. 24(6). 313–318. 22 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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