Laurent Magy

7.3k total citations
165 papers, 3.8k citations indexed

About

Laurent Magy is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Laurent Magy has authored 165 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Neurology, 75 papers in Cellular and Molecular Neuroscience and 31 papers in Physiology. Recurrent topics in Laurent Magy's work include Peripheral Neuropathies and Disorders (72 papers), Hereditary Neurological Disorders (69 papers) and Botulinum Toxin and Related Neurological Disorders (24 papers). Laurent Magy is often cited by papers focused on Peripheral Neuropathies and Disorders (72 papers), Hereditary Neurological Disorders (69 papers) and Botulinum Toxin and Related Neurological Disorders (24 papers). Laurent Magy collaborates with scholars based in France, United States and Algeria. Laurent Magy's co-authors include Jean‐Michel Vallat, Stéphane Mathis, Claudia Sommer, Laurence Richard, J.M. Vallat, Pierre‐Marie Preux, Claire Demiot, P. Couratier, B. Beaufrère and Yves Boirie‌ and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Laurent Magy

153 papers receiving 3.7k citations

Peers

Laurent Magy

NEURO

CMN

PFM

PHYSI

Jean‐Michel Vallat France

Chiara Briani Italy

Angelo Schenone Italy

Luís Querol Spain

Bruno Giometto Italy

Setsu Sawai Japan

Sonoko Misawa Japan

Tanya Stojkovic France

José Boucraut France

Saud Sadiq United States

Jean‐Michel Vallat France

Laurent Magy

2.3k ×1.1

NEURO

2.2k ×1.6

CMN

285 ×0.5

PFM

914 ×1.6

377 ×0.8

PHYSI

Citations per year, relative to Laurent Magy Laurent Magy (= 1×) peers Jean‐Michel Vallat

Countries citing papers authored by Laurent Magy

Since Specialization

Citations

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

Fields of papers citing papers by Laurent Magy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurent Magy

This figure shows the co-authorship network connecting the top 25 collaborators of Laurent Magy. A scholar is included among the top collaborators of Laurent Magy 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 Laurent Magy. Laurent Magy 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

Péréon, Yann, David Adams, Jean‐Philippe Camdessanché, et al.. (2025). Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study. Orphanet Journal of Rare Diseases. 20(1). 95–95. 1 indexed citations

Magy, Laurent, et al.. (2024). Early Peripheral Nerve Involvement at the Time of Coughing in Patients With RFC1 Intronic Expansion. Neurology Genetics. 10(4). e200166–e200166.

Richard, Laurence, Franck Sturtz, Laurent Magy, et al.. (2024). Neuroprotective Effect of Polyvalent Immunoglobulins on Mouse Models of Chemotherapy-Induced Peripheral Neuropathy. Pharmaceutics. 16(1). 139–139. 3 indexed citations

Guilleminault, Laurent, et al.. (2024). Cerebellar ataxia, neuropathy and vestibular areflexia syndrome: a neurogenic cough prototype. ERJ Open Research. 10(4). 24–2024. 2 indexed citations

Bonello‐Palot, Nathalie, Yann Péréon, Andoni Echaniz‐Laguna, et al.. (2023). Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease. European Journal of Neurology. 30(10). 3265–3276. 1 indexed citations

Attarian, Shahram, Peter Young, Thomas H. Brannagan, et al.. (2021). A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A. Orphanet Journal of Rare Diseases. 16(1). 433–433. 31 indexed citations

Vignaud, Guillaume, É. Liozon, Laurent Magy, et al.. (2017). Contribution of dot-blot assay to the diagnosis and management of myositis: a three-year practice at a university hospital centre.. PubMed. 34(5). 918–924. 3 indexed citations

Guedj, Mickaël, Viviane Bertrand, Julie Foucquier, et al.. (2017). A Rasch Analysis of the Charcot-Marie-Tooth Neuropathy Score (CMTNS) in a Cohort of Charcot-Marie-Tooth Type 1A Patients. PLoS ONE. 12(1). e0169878–e0169878. 14 indexed citations

Duchesne, Mathilde, Stéphane Mathis, Laurence Richard, et al.. (2017). Nerve Biopsy Is Still Useful in Some Inherited Neuropathies. Journal of Neuropathology & Experimental Neurology. 77(2). 88–99. 13 indexed citations

10.

Mandel, Jonas, Viviane Bertrand, Philippe Lehert, et al.. (2015). A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment. Orphanet Journal of Rare Diseases. 10(1). 74–74. 15 indexed citations

11.

Mathis, Stéphane, Benoît Funalot, Olivia Boyer, et al.. (2014). Neuropathologic Characterization ofINF2-Related Charcot-Marie-Tooth Disease: Evidence for a Schwann Cell Actinopathy. Journal of Neuropathology & Experimental Neurology. 73(3). 223–233. 25 indexed citations

12.

Danigo, Aurore, Laurent Magy, & Claire Demiot. (2013). TRPV1 dans les neuropathies douloureuses. médecine/sciences. 29(6-7). 597–606. 7 indexed citations

13.

Jamilloux, Yvan, Laurent Magy, Jean‐François Hurtevent, et al.. (2013). Immunological profiles determine neurological involvement in Sjögren's syndrome. European Journal of Internal Medicine. 25(2). 177–181. 41 indexed citations

14.

Mathis, Stéphane, et al.. (2011). Amyloid neuropathy mimicking chronic inflammatory demyelinating polyneuropathy. Muscle & Nerve. 45(1). 26–31. 70 indexed citations

15.

Magy, Laurent, Laurence Richard, & Jean‐Michel Vallat. (2011). Intérêt de la biopsie cutanée dans le diagnostic des neuropathies des petites fibres. La Presse Médicale. 41(6). 575–579. 5 indexed citations

16.

Fouillade, Charles, Hugues Chabriat, Florence Riant, et al.. (2008). Activating NOTCH3 mutation in a patient with small-vessel-disease of the Brain. Human Mutation. 29(3). 452–452. 48 indexed citations

17.

Magy, Laurent. (2006). Échelles fonctionnelles et neuropathies périphériques. Revue Neurologique. 162(4). 495–501. 1 indexed citations

18.

Magy, Laurent, F. Vincent, Sébastien Faure, et al.. (2005). The Renin-Angiotensin Systems: Evolving Pharmacological Perspectives for Cerebroprotection. Current Pharmaceutical Design. 11(25). 3275–3291. 16 indexed citations

19.

Vallat, Jean‐Michel, et al.. (2003). Intérêt de la biopsie nerveuse pour le diagnostic des formes atypiques de polyradiculonévrite inflammatoire démyélinisante chronique : 8 cas. Bulletin de l Académie Nationale de Médecine. 187(2). 387–403. 3 indexed citations

20.

Magy, Laurent, et al.. (2003). Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 cases. European Journal of Neurology. 10(6). 677–685. 78 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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