Cécile Peccate

1.1k total citations
25 papers, 661 citations indexed

About

Cécile Peccate is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Cécile Peccate has authored 25 papers receiving a total of 661 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Oncology. Recurrent topics in Cécile Peccate's work include Muscle Physiology and Disorders (15 papers), RNA Research and Splicing (10 papers) and Virus-based gene therapy research (6 papers). Cécile Peccate is often cited by papers focused on Muscle Physiology and Disorders (15 papers), RNA Research and Splicing (10 papers) and Virus-based gene therapy research (6 papers). Cécile Peccate collaborates with scholars based in France, United Kingdom and United States. Cécile Peccate's co-authors include Stéphanie Lorain, Luis Garcı́a, France Leturcq, S. Llense, Dominique Récan, Christophe Béroud, Guillaume Précigout, Thomas Voït, Bruno Cadot and Jean‐Claude Kaplan and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and PLoS ONE.

In The Last Decade

Cécile Peccate

25 papers receiving 649 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cécile Peccate France 15 560 112 110 86 73 25 661
Kristin N. Heller United States 14 569 1.0× 180 1.6× 137 1.2× 91 1.1× 51 0.7× 20 644
Quan Q. Gao United States 15 649 1.2× 85 0.8× 116 1.1× 67 0.8× 57 0.8× 20 749
Nicolas Wein United States 17 639 1.1× 146 1.3× 126 1.1× 134 1.6× 32 0.4× 34 684
Ryan D. Wuebbles United States 13 404 0.7× 54 0.5× 77 0.7× 81 0.9× 39 0.5× 22 468
Michael J. Petrany United States 7 535 1.0× 75 0.7× 55 0.5× 82 1.0× 82 1.1× 8 621
James S. Novak United States 14 599 1.1× 69 0.6× 81 0.7× 92 1.1× 49 0.7× 21 678
Juergen Scharner United Kingdom 13 625 1.1× 81 0.7× 46 0.4× 102 1.2× 50 0.7× 13 712
Patrizia Barzaghi Switzerland 8 555 1.0× 76 0.7× 79 0.7× 51 0.6× 132 1.8× 9 653
Hui Meng United States 17 593 1.1× 101 0.9× 211 1.9× 145 1.7× 157 2.2× 33 762
Dwi U. Kemaladewi Netherlands 11 515 0.9× 164 1.5× 55 0.5× 66 0.8× 35 0.5× 16 609

Countries citing papers authored by Cécile Peccate

Since Specialization
Citations

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

Fields of papers citing papers by Cécile Peccate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Peccate

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Peccate. A scholar is included among the top collaborators of Cécile Peccate 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 Cécile Peccate. Cécile Peccate 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.
Guigue, Philippe, Karim Harhouri, Cécile Peccate, et al.. (2024). Inhibition of poly(ADP-Ribosyl)ation reduced vascular smooth muscle cells loss and improves aortic disease in a mouse model of human accelerated aging syndrome. Cell Death and Disease. 15(10). 723–723. 3 indexed citations
2.
Garcia, Pauline, Caroline Brun, Lorenzo Giordani, et al.. (2024). Setdb1 protects genome integrity in murine muscle stem cells to allow for regenerative myogenesis and inflammation. Developmental Cell. 59(17). 2375–2392.e8. 6 indexed citations
3.
Peccate, Cécile, Anne Forand, Laura Julien, et al.. (2022). Muscle regeneration affects Adeno Associated Virus 1 mediated transgene transcription. Scientific Reports. 12(1). 9674–9674. 8 indexed citations
4.
Dour, Caroline Le, Maria Chatzifrangkeskou, Maria M. Magiera, et al.. (2022). Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations. Nature Communications. 13(1). 7886–7886. 34 indexed citations
5.
Ebrahimi, Majid, Dilani G. Gamage, Cécile Peccate, et al.. (2021). TGFβ signaling curbs cell fusion and muscle regeneration. Nature Communications. 12(1). 750–750. 81 indexed citations
6.
Wang, Kun, Gervaise Mosser, Bernard Haye, et al.. (2020). Self-assembly/condensation interplay in nano-to-microfibrillar silicified fibrin hydrogels. International Journal of Biological Macromolecules. 164. 1422–1431. 13 indexed citations
7.
Forand, Anne, Antoine Muchir, Nathalie Mougenot, et al.. (2020). Combined Treatment with Peptide-Conjugated Phosphorodiamidate Morpholino Oligomer-PPMO and AAV-U7 Rescues the Severe DMD Phenotype in Mice. Molecular Therapy — Methods & Clinical Development. 17. 695–708. 14 indexed citations
8.
Barthélémy, Inès, Nadège Calmels, Robert B. Weiss, et al.. (2020). X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation. Skeletal Muscle. 10(1). 23–23. 13 indexed citations
9.
Julien, Laura, Cécile Peccate, Stéphanie Lorain, et al.. (2018). RFX1 and RFX3 Transcription Factors Interact with the D Sequence of Adeno-Associated Virus Inverted Terminal Repeat and Regulate AAV Transduction. Scientific Reports. 8(1). 210–210. 8 indexed citations
10.
Trochet, Delphine, Bernard Prudhon, Maud Beuvin, et al.. (2017). Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy. EMBO Molecular Medicine. 10(2). 239–253. 43 indexed citations
11.
Peccate, Cécile, Laura Julien, Graham McClorey, et al.. (2016). Antisense pre-treatment increases gene therapy efficacy in dystrophic muscles. Human Molecular Genetics. 25(16). 3555–3563. 29 indexed citations
12.
13.
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
14.
Lorain, Stéphanie, Pascal Chappert, Romain Hardet, et al.. (2014). Intrinsic Transgene Immunogenicity Gears CD8+ T-cell Priming After rAAV-Mediated Muscle Gene Transfer. Molecular Therapy. 23(4). 697–706. 17 indexed citations
15.
Lorain, Stéphanie, Cécile Peccate, Graziella Griffith, et al.. (2013). Dystrophin rescue by trans -splicing: a strategy for DMD genotypes not eligible for exon skipping approaches. Nucleic Acids Research. 41(17). 8391–8402. 28 indexed citations
16.
Goyenvalle, Aurélie, Cécile Peccate, Guillaume Précigout, et al.. (2013). AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy. Molecular Therapy. 21(8). 1551–1558. 49 indexed citations
17.
Lorain, Stéphanie, et al.. (2010). Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts. PLoS ONE. 5(5). e10894–e10894. 25 indexed citations
18.
Lorain, Stéphanie, et al.. (2010). O.14 Exon exchange approach to repair Duchenne dystrophin transcripts. Neuromuscular Disorders. 20(9-10). 639–639. 1 indexed citations
19.
Llense, S., Dominique Récan, Cécile Peccate, et al.. (2006). Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. Human Mutation. 28(2). 183–195. 95 indexed citations
20.
Béroud, Christophe, Alain Carrié, Chérif Beldjord, et al.. (2003). Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene. Neuromuscular Disorders. 14(1). 10–18. 42 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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