Cyriaque Beley

1.3k total citations
18 papers, 653 citations indexed

About

Cyriaque Beley is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Cyriaque Beley has authored 18 papers receiving a total of 653 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Genetics. Recurrent topics in Cyriaque Beley's work include Muscle Physiology and Disorders (10 papers), Virus-based gene therapy research (5 papers) and RNA Research and Splicing (5 papers). Cyriaque Beley is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Virus-based gene therapy research (5 papers) and RNA Research and Splicing (5 papers). Cyriaque Beley collaborates with scholars based in France, United States and Germany. Cyriaque Beley's co-authors include Luis Garcı́a, Luis García, Rachid Benchaouir, Thomas Voït, Gillian Butler‐Browne, Stéphane Blot, Arnaud F. Klein, Christian Pinset, Hiroyuki Sorimachi and Eiichi KIMURA and has published in prestigious journals such as PLoS ONE, Molecular and Cellular Biology and Development.

In The Last Decade

Cyriaque Beley

18 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cyriaque Beley France 14 573 183 122 121 116 18 653
Jérôme Poupiot France 14 589 1.0× 210 1.1× 118 1.0× 113 0.9× 81 0.7× 21 668
Eric R. Pozsgai United States 10 567 1.0× 229 1.3× 79 0.6× 34 0.3× 136 1.2× 19 634
Angela Lek United States 14 686 1.2× 70 0.4× 59 0.5× 169 1.4× 72 0.6× 24 813
William Coley United States 14 532 0.9× 53 0.3× 112 0.9× 110 0.9× 41 0.4× 16 766
Pablo Morales United States 8 397 0.7× 281 1.5× 69 0.6× 34 0.3× 235 2.0× 17 638
Béatrice Joussemet France 6 413 0.7× 373 2.0× 73 0.6× 40 0.3× 193 1.7× 9 642
Juliette Hordeaux United States 13 496 0.9× 514 2.8× 138 1.1× 48 0.4× 106 0.9× 23 842
Fraser J. Wilkes United Kingdom 7 542 0.9× 353 1.9× 99 0.8× 27 0.2× 170 1.5× 7 695
Takako I. Jones United States 19 909 1.6× 120 0.7× 93 0.8× 26 0.2× 242 2.1× 32 948
Michael J. Petrany United States 7 535 0.9× 75 0.4× 34 0.3× 82 0.7× 82 0.7× 8 621

Countries citing papers authored by Cyriaque Beley

Since Specialization
Citations

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

Fields of papers citing papers by Cyriaque Beley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyriaque Beley

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

All Works

18 of 18 papers shown
1.
Goyenvalle, Aurélie, Andreas Marg, Cyriaque Beley, et al.. (2018). Exon Skipping in a Dysf-Missense Mutant Mouse Model. Molecular Therapy — Nucleic Acids. 13. 198–207. 20 indexed citations
2.
Stantzou, Amalia, Elija Schirwis, Sandra Swist, et al.. (2017). BMP signaling regulates satellite cell-dependent postnatal muscle growth. Development. 144(15). 2737–2747. 41 indexed citations
3.
Relizani, Karima, et al.. (2016). Rapid, scalable, and low-cost purification of recombinant adeno-associated virus produced by baculovirus expression vector system. Molecular Therapy — Methods & Clinical Development. 3. 16035–16035. 17 indexed citations
4.
Meregalli, Mirella, Andrea Farini, Clementina Sitzia, et al.. (2015). Stem Cell-Mediated Exon Skipping of the Dystrophin Gene by the Bystander Effect. Current Gene Therapy. 15(6). 563–571. 1 indexed citations
5.
Précigout, Guillaume, et al.. (2015). Simple downstream process based on detergent treatment improves yield and in vivo transduction efficacy of adeno-associated virus vectors. Molecular Therapy — Methods & Clinical Development. 2. 15024–15024. 25 indexed citations
6.
Philippi, Susanne, Stéphanie Lorain, Cyriaque Beley, et al.. (2015). Dysferlin rescue by spliceosome-mediated pre-mRNA trans-splicing targeting introns harbouring weakly defined 3′ splice sites. Human Molecular Genetics. 24(14). 4049–4060. 17 indexed citations
7.
Bajanca, Fernanda, Cyriaque Beley, Luis Garcı́a, et al.. (2015). In vivo dynamics of skeletal muscle Dystrophin in zebrafish embryos revealed by improved FRAP analysis. eLife. 4. 20 indexed citations
8.
Blázquez, Lorea, Ana Aiastui, María Goicoechea, et al.. (2013). In Vitro Correction of a Pseudoexon-Generating Deep Intronic Mutation in LGMD2A by Antisense Oligonucleotides and Modified Small Nuclear RNAs. Human Mutation. 34(10). 1387–1395. 18 indexed citations
9.
Li, Lina, Emilios K. Dimitriadis, Yu Yang, et al.. (2013). Production and Characterization of Novel Recombinant Adeno-Associated Virus Replicative-Form Genomes: A Eukaryotic Source of DNA for Gene Transfer. PLoS ONE. 8(8). e69879–e69879. 11 indexed citations
10.
Rendu, John, Julie Brocard, Éric Denarier, et al.. (2013). Exon Skipping as a Therapeutic Strategy Applied to an RYR1 Mutation with Pseudo-Exon Inclusion Causing a Severe Core Myopathy. Human Gene Therapy. 24(7). 702–713. 28 indexed citations
11.
Meregalli, Mirella, Claire Navarro, Clementina Sitzia, et al.. (2013). Full‐length dysferlin expression driven by engineered human dystrophic blood derived CD133+ stem cells. FEBS Journal. 280(23). 6045–6060. 7 indexed citations
12.
Vulin, Adeline, Inès Barthélémy, Aurélie Goyenvalle, et al.. (2012). Muscle Function Recovery in Golden Retriever Muscular Dystrophy After AAV1-U7 Exon Skipping. Molecular Therapy. 20(11). 2120–2133. 106 indexed citations
13.
Beley, Cyriaque, Robert M. Kotin, René Lai–Kuen, et al.. (2012). Human Galectin 3 Binding Protein Interacts with Recombinant Adeno-Associated Virus Type 6. Journal of Virology. 86(12). 6620–6631. 54 indexed citations
14.
Dumonceaux, Julie, Solenne Marie, Cyriaque Beley, et al.. (2010). Combination of Myostatin Pathway Interference and Dystrophin Rescue Enhances Tetanic and Specific Force in Dystrophic mdx Mice. Molecular Therapy. 18(5). 881–887. 54 indexed citations
15.
François, Virginie, Arnaud F. Klein, Cyriaque Beley, et al.. (2010). Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs. Nature Structural & Molecular Biology. 18(1). 85–87. 65 indexed citations
16.
Jarmin, Susan, Cyriaque Beley, Keith Foster, et al.. (2010). P06 Evaluation of the truncated products of exon and multiple exon skipping in DMD therapy. Neuromuscular Disorders. 20. S6–S6. 1 indexed citations
17.
Wein, Nicolas, Marc Bartoli, Cyriaque Beley, et al.. (2009). Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping. Human Mutation. 31(2). 136–142. 62 indexed citations
18.
Hérasse, Muriel, Yasuko Ono, Françoise Fougerousse, et al.. (1999). Expression and Functional Characteristics of Calpain 3 Isoforms Generated through Tissue-Specific Transcriptional and Posttranscriptional Events. Molecular and Cellular Biology. 19(6). 4047–4055. 106 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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