Guy Brochier

2.0k total citations
45 papers, 1.0k citations indexed

About

Guy Brochier is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Guy Brochier has authored 45 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Guy Brochier's work include Muscle Physiology and Disorders (15 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (8 papers). Guy Brochier is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (8 papers). Guy Brochier collaborates with scholars based in France, Italy and Argentina. Guy Brochier's co-authors include Emmanuelle Lacène, Norma B. Romero, Denis Dacheux, J. Croizé, Ina Attrée, Bertrand Toussaint, Jocelyn Laporte, Johann Böhm, Guy Lallement and Michel Fardeau and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Guy Brochier

45 papers receiving 987 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guy Brochier France 19 639 265 232 200 143 45 1.0k
Anke Seydel Italy 13 986 1.5× 124 0.5× 35 0.2× 135 0.7× 40 0.3× 18 1.4k
Alfredo Varela‐Echavarría Mexico 19 668 1.0× 523 2.0× 28 0.1× 182 0.9× 39 0.3× 68 1.4k
Yongqin Wu China 15 833 1.3× 315 1.2× 23 0.1× 124 0.6× 52 0.4× 27 1.5k
Anna Lyubetskaya United States 18 705 1.1× 98 0.4× 111 0.5× 107 0.5× 12 0.1× 21 1.7k
Mieko Yoshioka Japan 17 1.1k 1.7× 444 1.7× 167 0.7× 148 0.7× 139 1.0× 54 1.7k
Ken‐ichi Yagyu Japan 12 588 0.9× 604 2.3× 13 0.1× 196 1.0× 38 0.3× 32 1.3k
John Brennand United Kingdom 20 1.5k 2.3× 214 0.8× 30 0.1× 72 0.4× 61 0.4× 38 2.1k
Michael Stieß Germany 10 466 0.7× 364 1.4× 51 0.2× 277 1.4× 9 0.1× 14 937
William Wishart Switzerland 15 768 1.2× 142 0.5× 95 0.4× 57 0.3× 14 0.1× 22 1.4k

Countries citing papers authored by Guy Brochier

Since Specialization
Citations

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

Fields of papers citing papers by Guy Brochier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guy Brochier

This figure shows the co-authorship network connecting the top 25 collaborators of Guy Brochier. A scholar is included among the top collaborators of Guy Brochier 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 Guy Brochier. Guy Brochier 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.
Bui, Mai Thao, Gorka Fernández‐Eulate, Teresinha Evangelista, et al.. (2024). Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era. Acta Neuropathologica Communications. 12(1). 191–191. 1 indexed citations
2.
Bevilacqua, Jorge A., et al.. (2022). Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern. Neuromuscular Disorders. 32(8). 687–691. 3 indexed citations
3.
Etienne, Harry, Jésus Gonzalez‐Bermejo, Martin Dres, et al.. (2021). The terminal segment of the human phrenic nerve as a novel implantation site for diaphragm pacing electrodes: Anatomical and clinical description. Annals of Anatomy - Anatomischer Anzeiger. 239. 151835–151835. 4 indexed citations
4.
Lainé, Jeanne, Gilles Moulay, Michaël Trichet, et al.. (2019). Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle. Molecular Biology of the Cell. 30(5). 579–590. 36 indexed citations
5.
Berardo, Andrés, Xavière Lornage, Mridul Johari, et al.. (2019). HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes. Journal of Neurology. 266(10). 2524–2534. 19 indexed citations
6.
Garibaldi, Matteo, John Rendu, Julie Brocard, et al.. (2019). ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies. Acta Neuropathologica Communications. 7(1). 3–3. 33 indexed citations
7.
Carvalho, Alzira Alves de Siqueira, Guy Brochier, Konstantinos Papadopoulos, et al.. (2018). Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort. Genetic Testing and Molecular Biomarkers. 22(6). 374–383. 16 indexed citations
8.
Rossi, Daniela, Johanna Palmio, Anni Evilä, et al.. (2017). A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy. PLoS ONE. 12(10). e0186642–e0186642. 29 indexed citations
9.
Richard, Pascale, Capucine Trollet, Teresa Gidaro, et al.. (2015). PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling. Journal of Neuromuscular Diseases. 2(2). 175–180. 15 indexed citations
10.
Malfatti, Edoardo, Johann Böhm, Emmanuelle Lacène, et al.. (2015). A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy. Journal of Neuromuscular Diseases. 2(3). 219–227. 67 indexed citations
11.
Hernández‐Laín, Aurelio, Isabelle Husson, Nicole Monnier, et al.. (2010). de novo RYR1 heterozygous mutation (I4898T) causing lethal core–rod myopathy in twins. European Journal of Medical Genetics. 54(1). 29–33. 38 indexed citations
12.
Baille, Valérie, Robert Clarke, Guy Brochier, et al.. (2005). Soman-induced convulsions: The neuropathology revisited. Toxicology. 215(1-2). 1–24. 92 indexed citations
13.
Novotová, Marta, et al.. (2002). Joint participation of mitochondria and sarcoplasmic reticulum in the formation of tubular aggregates in gastrocnemius muscle of CK–/– mice. European Journal of Cell Biology. 81(2). 101–106. 18 indexed citations
14.
Gauthier, Yves, Ralf Matthias Hagen, Guy Brochier, et al.. (2001). Study on the pathophysiology of experimentalBurkholderia pseudomalleiinfection in mice. FEMS Immunology & Medical Microbiology. 30(1). 53–63. 21 indexed citations
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Brochier, Guy, Maurice Israël, & B. Lesbats. (1993). Immunolabelling of the presynaptic membrane of Torpedo electric organ nerve terminals with an antiserum towards the acetylcholine releasing protein mediatophore. Biology of the Cell. 78(3). 145–154. 34 indexed citations
19.
Morel, N., Guy Brochier, Monique Synguélakis, & G. Le Gal La Salle. (1991). Immunological identification of a new 14×103Mr membrane-bound protein in Torpedo electric organ. Journal of Cell Science. 98(3). 351–361. 13 indexed citations
20.
Y, Sultan, White Gc, A. Aronstam, et al.. (1986). Hemophilic patients with an inhibitor to factor VIII treated with high dose factor VIII concentrate. Results of a collaborative study for the evaluation of factor VIII inhibitor titer, recovery and half life of infused factor VIII.. PubMed. 28(2). 85–9. 7 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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