B. Estournet

5.5k citations

72 papers · 2.9k indexed · h-index 27

Genetics top 2%
- Neurogenetic and Muscular Disorders Research 22
Molecular Biology top 5%
- Muscle Physiology and Disorders 28
- Nuclear Structure and Function 11
- RNA Research and Splicing 5
Cardiology and Cardiovascular Medicine top 2%
- Cardiomyopathy and Myosin Studies 13
Immunology and Allergy top 5%
Cellular and Molecular Neuroscience top 5%
Neurology
- Myasthenia Gravis and Thymoma 7
Pulmonary and Respiratory Medicine
- Neonatal Respiratory Health Research 6
- Respiratory Support and Mechanisms 4

Co-authors: Pascale Guicheney Norma B. Romero A Barois Martin Brockington Thomas Voit Susana Quijano‐Roy Ana Ferreiro Francesco Muntoni
Cited by: Genetics Molecular Biology Cardiology and Cardiovascular Medicine
Journals: Neuromuscular Disorders (16 papers)Annals of Neurology (6 papers)Muscle & Nerve (3 papers)
Partner nations: France Italy United Kingdom

In The Last Decade

B. Estournet

67 papers receiving 2.9k citations

Peers

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

The 25 scholars most cited alongside B. Estournet, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with B. Estournet Line = papers co-authored together B. Estournet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Diaphragmatic dysfunction in SEPN1-related myopathy Neuromuscular Disorders ·Serena Caggiano,Sonia Khirani,Ivana Dabaj,Panfilo,Alessandro Amaddeo,Jorge Olmo Arroyo,Isabelle Desguerre,Pascale Richard,Renato Cutrera,Ana Ferreiro,B. Estournet,Susana Quijano-Roy,Hamid Mohamed	2017	30
2	Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 Children Journal of Neuromuscular Diseases ·Michela Catteruccia,Carole Vuillerot,Isabelle Vaugier,Ade Winayah,Liwen Zhang,Louis Viollet,B. Estournet,Enrico Bertini,Susana Quijano‐Roy	2015	21
3	Congenital myasthenic syndromes Handbook of clinical neurology ·B. Eymard,Daniel Hantaı̈,B. Estournet	2013	39
4	Diaphragmatic dysfunction in Collagen VI myopathies Neuromuscular Disorders ·Susana Quijano‐Roy,Sonia Khirani,Marina Colella,Adriana Ramirez,A. Alcalde Molina,Olumuyiwa Igbalajobi,Alix de Becdelièvre,Robert Carlier,Valérie Allamand,Pascale Richard,Liwen Zhang,B. Estournet,Brigitte Fauroux	2013	29
5	Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation European Journal of Human Genetics ·Rabah Ben Yaou,Claire Navarro,Susana Quijano-Roy,A. Bertrand,Catherine Massart,Annachiara De Sandre‐Giovannoli,Juan Cadiñanos,Kamel Mamchaoui,Gillian Butler‐Browne,B. Estournet,Pascale Richard,A Barois,Nicolas Lévy,Gisèle Bonne	2011	36
6	Riluzole pharmacokinetics in young patients with spinal muscular atrophy British Journal of Clinical Pharmacology ·Chadi Abbara,B. Estournet,Lucette Lacomblez,Bénédicte Lelièvre,Rüştü Güner,Blandine Lehmann,Louis Viollet,A Barois,Bertrand Diquet	2010	20
7	Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype Neuromuscular Disorders ·Sandrine Vuillaumier‐Barrot,Susana Quijano-Roy,C. Bouchet-Séraphin,Svetlana Maugenre,N. Yu. Yutanov,Peter Van den Bergh,Pascale Marcorelles,Daniela Avila‐Smirnow,C. L. Lima,Norma B. Romero,R. Carlier,B. Estournet,Pascale Guicheney,Nathalie Séta	2009	30
8	C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy Neuromuscular Disorders ·Valérie Allamand,Corine Gartioux,Emmanuelle Lacène,Jeanne Lainé,C. Ledeuil,Susana Quijano‐Roy,S. Makri,Louis Viollet,Pierre‐Yves Jeannet,Ульяна Андреевна Терещенко,C B CHRISTENSEN,Pascale Richard,B. Estournet,Norma B. Romero,Pascale Guicheney	2007	1
9	Protein O-mannosyltransferase activities in lymphoblasts from patients with α-dystroglycanopathies Neuromuscular Disorders ·Hiroshi Manya,C Bouchet,Aklass Dara,Sandrine Vuillaumier‐Barrot,Susana Quijano‐Roy,Yasushi Suzuki,Svetlana Maugenre,Pascale Richard,Toshiyuki Inazu,Luciano Merlini,Norma B. Romero,France Leturcq,MIRZA ABDUL QAYYUM,Haluk Topaloğlu,B. Estournet,Nathalie Séta,Tamao Endo,Pascale Guicheney	2007	25
10	C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy Annals of Neurology ·Virginie Carmignac,Mustafa A. Salih,Susana Quijano‐Roy,Sylvie Marchand,Diogo Silva de Aguiar Nobre,Maowia M. Mukhtar,Jon Andoni Urtizberea,Siegfried Labeit,Pascale Guicheney,France Leturcq,Mathias Gautel,Michel Fardeau,Kevin P. Campbell,Isabelle Richard,B. Estournet,Ana Ferreiro	2007	156
11	SEPN1: Associated with congenital fiber‐type disproportion and insulin resistance Annals of Neurology ·Nigel F. Clarke,Warren Kidson,Susana Quijano‐Roy,B. Estournet,Ana Ferreiro,Pascale Guicheney,James Manson,Andrew J. Kornberg,Lloyd K. Shield,Kathryn N. North	2006	114
12	Brain MRI abnormalities in muscular dystrophy due to FKRP mutations Brain and Development ·Susana Quijano‐Roy,Itxaso Martì,S. Makri,M. Mayer,Svetlana Maugenre,Pascale Richard,C. Bérard,Louis Viollet,Bruno Leheup,Pascale Guicheney,Jean-Marc Pinard,B. Estournet,Robert Carlier	2005	26
13	New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families Neurogenetics ·Chahnez Triki,Susana Quijano‐Roy,Pascale Richard,S. Makri,Jakob Ribič,Pascale Guicheney,Angela D Stultz,Maurice A. Schwartz,(unknown),B. Estournet,Hammadi Ayadi,Subir Mukhopadhyay	2004	65
14	Long‐term noninvasive mechanical ventilation for children at home: A national survey Pediatric Pulmonology ·Brigitte Fauroux,Adelaide Oduro-Asante,Isabelle Desguerre,B. Estournet,Ha Trang	2003	93
15	Phenotypic spectrum associated with mutations in the fukutin‐related protein gene Annals of Neurology ·Eugenio Mercuri,Martin Brockington,Volker Straub,Susana Quijano‐Roy,Yeliz Yuva,Ralf Herrmann,S. Brown,Silvia Torelli,Victor Dubowitz,Derek J. Blake,Norma B. Romero,B. Estournet,Caroline A. Sewry,Pascale Guicheney,Thomas Voit,Francesco Muntoni	2003	172
16	Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency Neuromuscular Disorders ·Susana Quijano‐Roy,Lucía Galán,Ana Ferreiro,F. Chéliout-Héraut,Françoise Gray,Michel Fardeau,A Barois,Pascale Guicheney,Norma B. Romero,B. Estournet	2002	20
17	Genetic characterisation of multi-minicore disease: identification of a first locus and evidence for genetic heterogeneity UCL Discovery (University College London) ·Ana Ferreiro,B. Estournet,C Laroche,Sophia Lin,H. N. Noristani,Hala Dheyaa,Nathalie Goemans,Heinz Jungbluth,R A Kaur,Luciano Merlini,Haluk Topaloğlu,T. Voit,Michel Fardeau,Pascale Guicheney	2001	1
18	Prognostic value of evoked potentials and sleep recordings in the prolonged comatose state of children. Preliminary data Neurophysiologie Clinique ·F. Chéliout-Héraut,Renata Rubinsztajn,Christine Ioos,B. Estournet	2001	32
19	Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency. Radiology ·А. В. Изатулин,Robert Carlier,Jean-Marc Pinard,D. Mompoint,N. A. Estrada-Alfaro,Emmanuel Burdairon,B. Estournet,A Barois,C. Vallée	1998	28
20	Ondine's Curse: A Discussion of Five Cases Neuropediatrics ·Ghulam Maulana Ilman,A Randaline,B. Estournet,A Barois	1993	22

About B. Estournet

B. Estournet is a scholar working on Genetics, Neurology, Anatomy, Aging and Cardiology and Cardiovascular Medicine, having authored 72 papers that have together received 2.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (28 papers), Neurogenetic and Muscular Disorders Research (22 papers), Cardiomyopathy and Myosin Studies (13 papers), Nuclear Structure and Function (11 papers), Myasthenia Gravis and Thymoma (7 papers), Neonatal Respiratory Health Research (6 papers), RNA Research and Splicing (5 papers) and Respiratory Support and Mechanisms (4 papers). The work is most often cited by research in Genetics (599 citations), Molecular Biology (2.2k citations), Cardiology and Cardiovascular Medicine (706 citations), Immunology and Allergy (156 citations) and Cellular and Molecular Neuroscience (450 citations). B. Estournet has collaborated with scholars based in France, Italy and United Kingdom. Frequent 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. Their work appears in journals such as Neuromuscular Disorders, Annals of Neurology, Muscle & Nerve, Handbook of clinical neurology and The American Journal of Human Genetics.

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