C Bouchet

577 total citations
13 papers, 232 citations indexed

About

C Bouchet is a scholar working on Molecular Biology, Surgery and Cellular and Molecular Neuroscience. According to data from OpenAlex, C Bouchet has authored 13 papers receiving a total of 232 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Surgery and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in C Bouchet's work include Muscle Physiology and Disorders (4 papers), RNA modifications and cancer (2 papers) and Ubiquitin and proteasome pathways (2 papers). C Bouchet is often cited by papers focused on Muscle Physiology and Disorders (4 papers), RNA modifications and cancer (2 papers) and Ubiquitin and proteasome pathways (2 papers). C Bouchet collaborates with scholars based in France, Japan and Türkiye. C Bouchet's co-authors include Pascale Guicheney, Nathalie Séta, Norma B. Romero, Sandrine Vuillaumier‐Barrot, Tamao Endo, Susana Quijano‐Roy, France Leturcq, Jean‐Marie Cuisset, Michel Fardeau and Peter Van den Bergh and has published in prestigious journals such as Neurology, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

C Bouchet

13 papers receiving 230 citations

Peers

C Bouchet

NEURO

CMN

PHYSI

R. Mercelis Belgium

Sagnika Ghosh United States

J. Byeong United States

Huanzheng Li China

Mara Lúcia Schmitz Ferreira Santos Brazil

Kate Craig United Kingdom

Jack J. Collier United Kingdom

Celeste Panteghini Italy

A Barois France

Gösta Holmgren Sweden

R. Mercelis Belgium

C Bouchet

252 ×1.2

15 ×0.5

NEURO

73 ×2.3

54 ×1.9

CMN

14 ×0.5

PHYSI

Citations per year, relative to C Bouchet C Bouchet (= 1×) peers R. Mercelis

Countries citing papers authored by C Bouchet

Since Specialization

Citations

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

Fields of papers citing papers by C Bouchet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Bouchet

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

All Works

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13 of 13 papers shown

Clarke, Nigel F., Svetlana Maugenre, Aurélie Vandebrouck, et al.. (2011). Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene. European Journal of Human Genetics. 19(4). 452–457. 40 indexed citations

Bouchet, C, Susana Quijano‐Roy, Sandrine Vuillaumier‐Barrot, et al.. (2008). POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardation. European Journal of Medical Genetics. 52(4). 201–206. 20 indexed citations

Manya, Hiroshi, C Bouchet, Sandrine Vuillaumier‐Barrot, et al.. (2007). Protein O-mannosyltransferase activities in lymphoblasts from patients with α-dystroglycanopathies. Neuromuscular Disorders. 18(1). 45–51. 25 indexed citations

Bouchet, C, Peter Van den Bergh, Jean‐Marie Cuisset, et al.. (2007). New POMT2 mutations causing congenital muscular dystrophy. Neurology. 69(12). 1254–1260. 44 indexed citations

Bouchet, C, Julie Steffann, Sophie Monnot, et al.. (2006). Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development. Journal of Medical Genetics. 43(10). 788–792. 34 indexed citations

Bouchet, C, Sandrine Vuillaumier‐Barrot, M. Gonzalés, et al.. (2006). Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families. Molecular Genetics and Metabolism. 90(1). 93–96. 17 indexed citations

Rodriguez, Matías, Katell Peoc’h, Stéphane Haı̈k, et al.. (2005). A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease. Neurology. 64(8). 1455–1457. 40 indexed citations

Jourdan, C, et al.. (1992). [A comparative study of CPK during spinal surgery in the knee-chest position. Apropos of 93 patients].. PubMed. 40(2). 87–90. 1 indexed citations

Philippon, B., et al.. (1989). [Effects of an intravenous injection of nicardipine on cerebral blood flow in subarachnoid hemorrhage caused by intracranial aneurysm].. PubMed. 30(7). 411–5. 4 indexed citations

10.

Grau, A, et al.. (1986). [Complications related to the seated position of the aged patient in neurosurgery].. PubMed. 34(3). 209–12. 2 indexed citations

11.

Bouchet, C, et al.. (1983). [Acute thrombosis of the aortic bifurcation caused by heparin allergy. Apropos of 5 cases].. PubMed. 120(11). 643–6. 1 indexed citations

12.

Aubert, M, et al.. (1982). [Instrumental perforations of the esophagus].. PubMed. 31(8). 567–72. 1 indexed citations

13.

Bouchet, C, et al.. (1981). [Intramural hematomas of the small bowel (duodenum excluded) during long-term anticoagulant treatment. Report on 6 cases of which 2 required operation (author's transl)].. PubMed. 118(5). 307–14. 3 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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