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Maud Beuvin

Observed names: Beuvin Maud, Beuvin, M, Beuvin, Maud, M. BEUVIN, M. Beuvin, Maud Beuvin Ms
Observed institutions: Centre National de la Recherche Scientifique, Nationwide Children's Hospital, University of Antwerp, Inserm, Sorbonne Université, BioCruces Health research Institute, Assistance Publique – Hôpitaux de Paris, Antwerp University Hospital, Institut de Myologie, Pitié-Salpêtrière Hospital, Tampere University Hospital, Genethon (France), University of Tampere, Centre de Recherche en Myologie, Université Pierre-et-Marie-Curie, Institute Born-Bunge, Abigail Wexner Research Institute, University College London, Newcastle University
ORCID: 0000-0002-5908-761X
Observed ORCID: 0000-0002-5908-761X
OpenAlex ID: A5023146149
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
2009 · Lucie Gueneau, Anne T. Bertrand, et al. · The American Journal of Human Genetics · 241
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Oxidative stress in SEPN1‐related myopathy: From pathophysiology to treatment
2009 · Sandrine Arbogast, Maud Beuvin, et al. · Annals of Neurology · 161
Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients
2014 · Caroline Le Guiner, Marie Montus, et al. · Molecular Therapy · 134
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice
2010 · Anne-Cécile Durieux, Alban Vignaud, et al. · Human Molecular Genetics · 132
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy
2016 · Vanessa Schartner, Norma B. Romero, et al. · Acta Neuropathologica · 130
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A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy
2015 · Edoardo Malfatti, Johann Böhm, et al. · Journal of Neuromuscular Diseases · 106
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Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency
2010 · Perrine Castets, Anne T. Bertrand, et al. · Human Molecular Genetics · 105
ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene
2016 · Maria Chatzifrangkeskou, Caroline Le Dour, et al. · Human Molecular Genetics · 103
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Activation of Rac1 by Paxillin-Crk-DOCK180 Signaling Complex Is Antagonized by Rap1 in Migrating NBT-II Cells
2004 · Ana M. Vallés, Maud Beuvin, et al. · Journal of Biological Chemistry · 95
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Dystrophin quantification
2014 · Karen Anthony, Virginia Arechavala-Gomeza, et al. · Neurology · 86
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DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death
2011 · Anne T. Bertrand, Laure Renou, et al. · Human Molecular Genetics · 79
Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy
2011 · Mathieu Rederstorff, Perrine Castets, et al. · PLoS ONE · 78
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Can phrenic stimulation protect the diaphragm from mechanical ventilation-induced damage?
2013 · Hicham Masmoudi, Catherine Coirault, et al. · European Respiratory Journal · 66
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de novo RYR1 heterozygous mutation (I4898T) causing lethal core–rod myopathy in twins
2010 · Aurelio Hernandez-Lain, Isabelle Husson, et al. · European Journal of Medical Genetics · 58
A new titinopathy
2015 · Rafael De Cid, Rabah Ben Yaou, et al. · Neurology · 57
Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
2017 · Delphine Trochet, Bernard Prudhon, et al. · EMBO Molecular Medicine · 56
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‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies
2019 · Matteo Garibaldi, John Rendu, et al. · Acta Neuropathologica Communications · 55
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Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy
2017 · Feriel Azibani, Astrid Brull, et al. · Molecular Therapy — Nucleic Acids · 39
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Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
2019 · Willem De Ridder, Isabelle Nelson, et al. · Neurology Genetics · 35
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Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies
2018 · Rainiero Ávila-Polo, Edoardo Malfatti, et al. · Journal of Neuropathology & Experimental Neurology · 32
Impaired excitation–contraction coupling in muscle fibres from the dynamin2R465W mouse model of centronuclear myopathy
2017 · Candice Kutchukian, Peter Szentesi, et al. · The Journal of Physiology · 32
A Muscle Hybrid Promoter as a Novel Tool for Gene Therapy
2019 · Katarzyna Piekarowicz, Anne T. Bertrand, et al. · Molecular Therapy — Methods & Clinical Development · 31
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Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies
2022 · Clémence Labasse, Guy Brochier, et al. · Acta Neuropathologica Communications · 26
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Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC
2016 · D. Avila-Smirnow, L. Gueneau, et al. · Revue Neurologique · 23
Prolonged mechanical ventilation worsens sepsis-induced diaphragmatic dysfunction in the rat
2018 · Matthieu Le Dinh, Serge Carreira, et al. · PLoS ONE · 20
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Works count: 105
Citation count: 2,113
H-index: 23
I10-index: 31
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