Gauthier Remiche

871 total citations
29 papers, 242 citations indexed

About

Gauthier Remiche is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Gauthier Remiche has authored 29 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Neurology and 8 papers in Physiology. Recurrent topics in Gauthier Remiche's work include Glycogen Storage Diseases and Myoclonus (7 papers), Lysosomal Storage Disorders Research (7 papers) and Peripheral Neuropathies and Disorders (5 papers). Gauthier Remiche is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (7 papers), Lysosomal Storage Disorders Research (7 papers) and Peripheral Neuropathies and Disorders (5 papers). Gauthier Remiche collaborates with scholars based in Belgium, United States and France. Gauthier Remiche's co-authors include Nicolas Mavroudakis, Marc Abramowicz, Giacomo P. Comi, Dario Ronchi, Frédéric Vandergheynst, Flavio Bellante, Stéphanie Delstanche, Christian Mélot, Guy Decaux and Jan De Bleecker and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Neurology and European Journal of Neurology.

In The Last Decade

Gauthier Remiche

26 papers receiving 234 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gauthier Remiche Belgium 10 96 81 71 48 46 29 242
David F. Kronn United States 7 114 1.2× 156 1.9× 62 0.9× 22 0.5× 21 0.5× 9 310
Gilberto Bultron United States 6 170 1.8× 60 0.7× 15 0.2× 78 1.6× 11 0.2× 9 389
Raül Santamaría Spain 9 244 2.5× 83 1.0× 22 0.3× 21 0.4× 13 0.3× 13 323
Liliana Vercelli Italy 9 47 0.5× 167 2.1× 43 0.6× 42 0.9× 5 0.1× 17 276
Emma Glamuzina New Zealand 11 68 0.7× 148 1.8× 76 1.1× 31 0.6× 6 0.1× 30 323
Margherita Stefania Rodolico Italy 10 125 1.3× 69 0.9× 31 0.4× 26 0.5× 31 0.7× 26 276
François Hallé France 9 64 0.7× 120 1.5× 61 0.9× 8 0.2× 11 0.2× 19 339
Masao Sakai Japan 8 132 1.4× 116 1.4× 208 2.9× 59 1.2× 55 1.2× 13 380
Y Ikura Japan 4 106 1.1× 151 1.9× 124 1.7× 56 1.2× 12 0.3× 6 355
Elena Mutti Italy 12 55 0.6× 201 2.5× 223 3.1× 46 1.0× 39 0.8× 25 393

Countries citing papers authored by Gauthier Remiche

Since Specialization
Citations

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

Fields of papers citing papers by Gauthier Remiche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gauthier Remiche

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

All Works

20 of 20 papers shown
1.
Peeters, Ronald, Nicolas Dubuisson, Peter Van den Bergh, et al.. (2024). Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient‐reported outcome measures. European Journal of Neurology. 31(7). e16282–e16282. 5 indexed citations
2.
Bleecker, Jan De, et al.. (2024). Recommendations for the management of myasthenia gravis in Belgium. Acta Neurologica Belgica. 124(4). 1371–1383. 10 indexed citations
3.
Delstanche, Stéphanie, Kristl G. Claeys, Jan De Bleecker, et al.. (2024). Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience. Acta Clinica Belgica. 79(6). 393–402.
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Stojkovic, Tanya, A. Nascimento, John Vissing, et al.. (2023). P424 Identify genetic modifiers controlling severity of collagen-6 related dystrophies (COL6-RD). Neuromuscular Disorders. 33. S158–S158.
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Vandernoot, Isabelle, et al.. (2020). Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation. Clinical Genetics. 98(4). 416–417. 1 indexed citations
10.
Fieuws, Steffen, Ann D’Hondt, Corinne Bleyenheuft, et al.. (2020). Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures. Orphanet Journal of Rare Diseases. 15(1). 83–83. 27 indexed citations
11.
Remiche, Gauthier, et al.. (2019). Late-onset Pompe disease associated with polyneuropathy. Neuromuscular Disorders. 29(12). 968–972. 7 indexed citations
12.
Bleyenheuft, Corinne, Philip Van Damme, Nathalie Goemans, et al.. (2018). Quantifying the changes in activity level of neuromuscular patients using the ACTIVLIM questionnaire: A 5-years study. Annals of Physical and Rehabilitation Medicine. 61. e541–e541. 1 indexed citations
13.
Vandergheynst, Frédéric, Flavio Bellante, Gaetano Perrotta, et al.. (2016). Impact of hyponatremia on nerve conduction and muscle strength. European Journal of Clinical Investigation. 46(4). 328–333. 35 indexed citations
14.
Remiche, Gauthier, Hazim Kadhim, Marc Abramowicz, et al.. (2015). A novel large deletion in the RYR1 gene in a Belgian family with late-onset and recessive core myopathy. Neuromuscular Disorders. 25(5). 397–402. 4 indexed citations
15.
Spada, Marco, Francesco Porta, Liliana Vercelli, et al.. (2013). Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia. Molecular Genetics and Metabolism. 109(2). 171–173. 35 indexed citations
16.
Remiche, Gauthier, Dario Ronchi, Francesca Magri, et al.. (2013). Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature. Journal of Neurology. 261(1). 83–97. 15 indexed citations
17.
Remiche, Gauthier, Marc Abramowicz, & Nicolas Mavroudakis. (2013). Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) associated to hereditary neuropathy with liability to pressure palsies (HNPP) and revealed after influenza AH1N1 vaccination. Acta Neurologica Belgica. 113(4). 519–522. 12 indexed citations
18.
Remiche, Gauthier, A. Lo Mauro, Paolo Tarsia, et al.. (2013). Postural effects on lung and chest wall volumes in late onset type II glycogenosis patients. Respiratory Physiology & Neurobiology. 186(3). 308–314. 12 indexed citations
19.
Vilain, Catheline, Alec Aeby, Patrick Van Bogaert, et al.. (2011). A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome. Clinical Genetics. 82(3). 264–270. 21 indexed citations
20.
Gaspard, Nicolas, et al.. (2011). Subacute gestational neuropathy: role of thiamine deficiency.. PubMed. 111(4). 349–52. 1 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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