Author

Arnaud Jacquier

Observed names: A. Jacquier, JACQUIER, Arnaud, Jacquier Arnaud, Jacquier, Arnaud, Jacquier,Arnaud

Institutions: Lyon 1 Université, Centre National de la Recherche Scientifique, Inserm, Hospices Civils de Lyon, Institut NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle

Observed institutions: Lyon 1 Université, Centre National de la Recherche Scientifique, Inserm, Université de Lyon, Aix-Marseille Université, Columbia University Irving Medical Center, Hospices Civils de Lyon, Institut de Biologie du Développement Marseille, Institut de Neurobiologie de la Méditerranée, Institut NeuroMyoGène, Institut de Neurosciences de la Timone, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, Institut NeuroMyoGène - Appui à la recherche, Columbia University

ORCID: 0000-0002-2883-9620

Observed ORCID: 0000-0002-2883-9620

OpenAlex ID: A5013299090

Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H

2007 · Valérie Delague, Arnaud Jacquier, et al. · The American Journal of Human Genetics · 161

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Inflammation in ALS and SMA: Sorting out the good from the evil

2009 · Dimitra Papadimitriou, Virginia Le Verche, et al. · Neurobiology of Disease · 132

PlexinA1 is a new Slit receptor and mediates axon guidance function of Slit C-terminal fragments

2014 · Céline Delloye-Bourgeois, Arnaud Jacquier, et al. · Nature Neuroscience · 119

Chronic activation in presymptomatic amyotrophic lateral sclerosis (ALS) mice of a feedback loop involving Fas, Daxx, and FasL

2006 · C. Raoul, E. Buhler, et al. · Proceedings of the National Academy of Sciences · 115

Alsin/Rac1 signaling controls survival and growth of spinal motoneurons

2006 · Arnaud Jacquier, Emmanuelle Buhler, et al. · Annals of Neurology · 77

Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies

2012 · Shingo Kariya, Diane B. Re, et al. · Human Molecular Genetics · 54

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Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow

2020 · Vartika Mishra, Diane B. Re, et al. · Nature Communications · 51

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The Regulatory Machinery of Neurodegeneration in In Vitro Models of Amyotrophic Lateral Sclerosis

2015 · Burcin Ikiz, Mariano J. Alvarez, et al. · Cell Reports · 49

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Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death

2017 · Arnaud Jacquier, Cécile Delorme, et al. · Acta Neuropathologica Communications · 32

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Novel combinatorial screening identifies neurotrophic factors for selective classes of motor neurons

2017 · Sébastien Schaller, Dorothée Buttigieg, et al. · Proceedings of the National Academy of Sciences · 32

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy

2022 · Arnaud Jacquier, Julian Theuriet, et al. · Brain · 29

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Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies

2022 · Arnaud Jacquier, Simon Roubille, et al. · Frontiers in Cellular Neuroscience · 26

Delivery of Prime editing in human stem cells using pseudoviral NanoScribes particles

2025 · Thibaut Halegua, Valérie Risson, et al. · Nature Communications · 23

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Astrocytic protection of spinal motor neurons but not cortical neurons against loss of Als2/alsin function

2009 · A. Jacquier, S. Bellouze, et al. · Human Molecular Genetics · 21

Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport

2016 · Michael K. Schäfer, Sarah Bellouze, et al. · Brain Pathology · 18

Nucleolar reorganization after cellular stress is orchestrated by SMN shuttling between nuclear compartments

2023 · Shaqraa Musawi, Lise-Marie Donnio, et al. · Nature Communications · 17

Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype

2021 · Menelaos Pipis, Andrea Cortese, et al. · Journal of Neurology Neurosurgery & Psychiatry · 17

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Expanding the phenotypic variability of MORC2 gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy

2022 · Arnaud Jacquier, Shams Ribault, et al. · Human Mutation · 15

Glutamate pathway implication in amyotrophic lateral sclerosis: what is the signal in the noise?

2010 · Diane Re, Virginia Le Verche, et al. · Journal of Receptor Ligand and Channel Research · 15

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Muscle fibroblasts and stem cells stimulate motor neurons in an age and exercise‐dependent manner

2024 · Casper Soendenbroe, Peter Schjerling, et al. · Aging Cell · 14

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Repurposing pentamidine using hyaluronic acid-based nanocarriers for skeletal muscle treatment in myotonic dystrophy

2022 · Mathieu Repellin, Flavia Carton, et al. · Nanomedicine Nanotechnology Biology and Medicine · 13

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons

2022 · Arnaud Jacquier, Valérie Risson, et al. · Acta Neuropathologica · 13

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Use of pHluorin to Assess the Dynamics of Axon Guidance Receptors in Cell Culture and in the Chick Embryo

2014 · Céline Delloye-Bourgeois, Arnaud Jacquier, et al. · Journal of Visualized Experiments · 10

Mitochondrial disorders are associated with morphological neuromuscular junction defects

2024 · Lola E. R. Lessard, Emmanuelle Girard, et al. · Neuromuscular Disorders · 9

Genetic characterization of non-5q proximal spinal muscular atrophy in a French cohort: the place of whole exome sequencing

2023 · Julian Theuriet, Gorka Fernandez-Eulate, et al. · European Journal of Human Genetics · 8

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Works count: 54

Citation count: 1,098

H-index: 17

I10-index: 23