B. Eymard

6.6k total citations
82 papers, 2.6k citations indexed

About

B. Eymard is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, B. Eymard has authored 82 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 28 papers in Cardiology and Cardiovascular Medicine and 23 papers in Cellular and Molecular Neuroscience. Recurrent topics in B. Eymard's work include Muscle Physiology and Disorders (32 papers), Cardiomyopathy and Myosin Studies (26 papers) and Genetic Neurodegenerative Diseases (21 papers). B. Eymard is often cited by papers focused on Muscle Physiology and Disorders (32 papers), Cardiomyopathy and Myosin Studies (26 papers) and Genetic Neurodegenerative Diseases (21 papers). B. Eymard collaborates with scholars based in France, Italy and Finland. B. Eymard's co-authors include Pascal Laforêt, Tanya Stojkovic, Karim Wahbi, Denis Duboc, Anthony Béhin, Christophe Meune, Christine Tranchant, Anne Lombès, Henri-Marc Bécane and Annick Toutain and has published in prestigious journals such as Nature, JAMA and Journal of Clinical Investigation.

In The Last Decade

B. Eymard

76 papers receiving 2.5k citations

Peers

Countries citing papers authored by B. Eymard

Since Specialization

Citations

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

Fields of papers citing papers by B. Eymard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of B. Eymard. A scholar is included among the top collaborators of B. Eymard 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. Eymard. B. Eymard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort 2023 ·European Journal of Neurology ·(unknown), (unknown), (unknown), Stéphane Vassilopoulos, Anthony Béhin, Céline Tard, Maud Michaud, (unknown), Savine Vicart, Marion Masingue, Robert‐Yves Carlier, Norma B. Romero, Emmanuelle Lacène, France Leturcq, B. Eymard, Pascal Laforêt, Tanya Stojkovic	4
2	Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies 2022 ·Neuromuscular Disorders ·Marion Masingue, Benoît Rucheton, Céline Bris, Norma B. Romero, Vincent Procaccio, B. Eymard	2
3	Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders 2019 ·PLoS ONE ·Abdallah Fayssoil, Lee S. Nguyen, Adam Ogna, Tanya Stojkovic, (unknown), D. Mompoint, Robert Carlier, Hélène Prigent, Bernard Clair, Anthony Béhin, Pascal Laforêt, Guillaume Bassez, Pascal Crenn, David Orlikowski, Djillali Annane, B. Eymard, Frédéric Lofaso	31
4	Life-threatening lactic acidosis occurring in adults with mitochondrial disorders 2019 ·Revue Neurologique ·(unknown), Anthony Béhin, Corinne Pottier, Claude Jardel, Tarek Sharshar, Fanny Mochel, (unknown), Abdelhamid Slama, Anne Lombès, B. Eymard, Pascal Laforêt	1
5	Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort 2018 ·Genetic Testing and Molecular Biomarkers ·Alzira Alves de Siqueira Carvalho, (unknown), Guy Brochier, (unknown), (unknown), (unknown), (unknown), Konstantinos Papadopoulos, Anthony Béhin, Pascal Laforêt, T. Stojkovic, B. Eymard, Michel Fardeau, Norma B. Romero	16
6	Hypertrophic cardiomyopathy in glycogen storage disease type III: Clinical features and long-term outcome 2018 ·Archives of Cardiovascular Diseases Supplements ·C. Chong-Nguyen, Abdallah Fayssoil, Pascal Laforêt, (unknown), François Petit, Arnaud Hubert, (unknown), Henri Marc Bécane, Tanya Stojkovic, B. Eymard, (unknown), Karim Wahbi	4
7	A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 2017 ·PLoS ONE ·Daniela Rossi, Johanna Palmio, Anni Evilä, Lucia Galli, Virginia Barone, (unknown), (unknown), (unknown), Christopher Berndsen, Nathan T. Wright, Edoardo Malfatti, Guy Brochier, Enrico Pierantozzi, Albena Jordanova, Velina Guergueltcheva, Norma B. Romero, Peter Hackman, B. Eymard, Bjarne Udd, Vincenzo Sorrentino	29
8	Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases 2015 ·Journal of Neuromuscular Diseases ·Isabelle Nelson, (unknown), (unknown), France Leturcq, Henri-Marc Bécane, Dominique Babuty, Annick Toutain, Christophe Béroud, Pascale Richard, Norma B. Romero, B. Eymard, Rabah Ben Yaou, Gisèle Bonne	26
9	Neutral lipid storage disease with myopathy: A whole-body nuclear MRI and metabolic study 2012 ·Molecular Genetics and Metabolism ·Pascal Laforêt, Tanya Stojkovic, Guillaume Bassez, Pierre G. Carlier, Karine Clément, Karim Wahbi, François Petit, B. Eymard, Robert‐Yves Carlier	26
10	Dilated cardiomyopathy in patients with mutations in anoctamin 5 2012 ·International Journal of Cardiology ·Karim Wahbi, Anthony Béhin, Henri Marc Bécane, France Leturcq, Mireille Cossée, Pascal Laforêt, Tanya Stojkovic, Pierre G. Carlier, (unknown), V. Gaxotte, P. Cluzel, B. Eymard, Denis Duboc	45
11	Electrophysiological Study With Prophylactic Pacing and Survival in Adults With Myotonic Dystrophy and Conduction System Disease 2012 ·JAMA ·Karim Wahbi, Christophe Meune, Raphaël Porcher, Henri Marc Bécane, Arnaud Lazarus, Pascal Laforêt, Tanya Stojkovic, Anthony Béhin, (unknown), B. Eymard, Denis Duboc	92
12	Long-term observational study of sporadic inclusion body myositis 2011 ·Brain ·Olivier Benvéniste, Marguerite Guiguet, (unknown), O. Dubourg, Waney Squier, Thierry Maisonobe, Tanya Stojkovic, Maria Isabel Leite, Yves Allenbach, S. Herson, Stefen Brady, B. Eymard, David Hilton‐Jones	227
13	Permanent muscle weakness in MCArdle disease 2009 ·Muscle & Nerve ·Aleksandra Nadaj‐Pakleza, (unknown), Pascal Laforêt, B. Eymard, Élisabeth Dion, Susana Teijeira, (unknown), Marc Jeanpierre, Carmen Navarro, Tanya Stojkovic	46
14	Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study 2009 ·Acta Neuropathologica ·Kristl G. Claeys, Peter F. M. van der Ven, Anthony Béhin, Tanya Stojkovic, B. Eymard, O. Dubourg, Pascal Laforêt, Georgine Faulkner, Pascale Richard, Patrick Vicart, Norma B. Romero, G. Stoltenburg, Bjarne Udd, Michel Fardeau, Thomas Voït, Dieter O. Fürst	54
15	Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency 2009 ·Neuromuscular Disorders ·Pascal Laforêt, Cécile Acquaviva, Odile Rigal, M. Brivet, I. Pénisson-Besnier, B. Chabrol, Denys Chaigne, Odile Boespflug‐Tanguy, Cécile Laroche, Anne‐Laure Bédat‐Millet, Anthony Béhin, I. Delèvaux, Anne Lombès, Brage Storstein Andresen, B. Eymard, Christine Vianey‐Saban	66
16	Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up 2007 ·American Heart Journal ·Denis Duboc, Christophe Meune, Bertrand Pierre, Karim Wahbi, B. Eymard, Annick Toutain, C. Bérard, Guy Vaksmann, Simon Weber, Henri-Marc Bécane	237
17	La dystrophie musculaire des ceintures autosomique dominante associée à des troubles de la conduction cardiaque (LGMD1B). Description de 8 nouvelles familles avec mutations du gène LMNA 2005 ·Revue Neurologique ·Rabah Ben Yaou, Henri Marc Bécane, L. Demay, Pascal Laforêt, Didier Hannequin, (unknown), Valérie Drouin‐Garraud, Xavier Ferrer, J.M. Mussini, (unknown), P. Petiot, I. Pénisson-Besnier, Nathalie Streichenberger, Annick Toutain, Pascale Richard, B. Eymard, Gisèle Bonne	12
18	Clinical study of chronic pain in hereditary myopathies 2003 ·European Journal of Pain ·Thierry Delorme, F. Boureau, B. Eymard, Pascal Laforêt, (unknown)	10
19	Clinical analysis of 32 patients carrying R453W LMNA mutation 2002 ·UCL Discovery (University College London) ·Gisèle Bonne, Rabah Ben Yaou, L. Demay, Pascale Richard, B. Eymard, J. Andoni Urtizberea, D Duboc, F. Muntoni, M Wehnert, (unknown), Luciano Merlini, (unknown), M. Visser, Dominique Récan, Kevin J. Schwartz	2
20	MR quantification of muscle fatty replacement in McArdle's disease 1996 ·Magnetic Resonance Imaging ·É. de Kerviler, Anne Leroy‐Willig, D Duboc, B. Eymard, André Syrota	21

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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