Frédérique Coppée

4.9k total citations
30 papers, 1.7k citations indexed

About

Frédérique Coppée is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Frédérique Coppée has authored 30 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Frédérique Coppée's work include Muscle Physiology and Disorders (16 papers), RNA Research and Splicing (12 papers) and RNA modifications and cancer (5 papers). Frédérique Coppée is often cited by papers focused on Muscle Physiology and Disorders (16 papers), RNA Research and Splicing (12 papers) and RNA modifications and cancer (5 papers). Frédérique Coppée collaborates with scholars based in Belgium, France and United States. Frédérique Coppée's co-authors include Alexandra Belayew, Eugénie Ansseau, Alexandra Tassin, Dalila Laoudj‐Chenivesse, Sébastien Sauvage, Denise A. Figlewicz, Christel Mattéotti, Oberdan Léo, Marietta Barro and Scott Q. Harper and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The EMBO Journal.

In The Last Decade

Frédérique Coppée

30 papers receiving 1.7k citations

Peers

Frédérique Coppée
Frédérique Coppée
Citations per year, relative to Frédérique Coppée Frédérique Coppée (= 1×) peers J.‐C. Kaplan

Countries citing papers authored by Frédérique Coppée

Since Specialization
Citations

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

Fields of papers citing papers by Frédérique Coppée

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédérique Coppée

This figure shows the co-authorship network connecting the top 25 collaborators of Frédérique Coppée. A scholar is included among the top collaborators of Frédérique Coppée 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 Frédérique Coppée. Frédérique Coppée 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.
Slavin, Moriya, Eugénie Ansseau, Saskia Lassche, et al.. (2023). The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins. Skeletal Muscle. 13(1). 5–5. 4 indexed citations
2.
Tassin, Alexandra, Eugénie Ansseau, Alexandra Belayew, et al.. (2020). Induction of a local muscular dystrophy using electroporation in vivo: an easy tool for screening therapeutics. Scientific Reports. 10(1). 11301–11301. 7 indexed citations
3.
Coppée, Frédérique, Jérôme R. Lechien, Anne‐Émilie Declèves, Lionel Tafforeau, & Sven Saussez. (2020). Severe acute respiratory syndrome coronavirus 2: virus mutations in specific European populations. New Microbes and New Infections. 36. 100696–100696. 17 indexed citations
4.
Vanderplanck, Céline, Alexandra Tassin, Eugénie Ansseau, et al.. (2018). Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei. Skeletal Muscle. 8(1). 2–2. 17 indexed citations
5.
Ansseau, Eugénie, Jocelyn O. Eidahl, Alexandra Tassin, et al.. (2016). Homologous Transcription Factors DUX4 and DUX4c Associate with Cytoplasmic Proteins during Muscle Differentiation. PLoS ONE. 11(1). e0146893–e0146893. 30 indexed citations
6.
Ansseau, Eugénie, Karlien Pieters, Céline Vanderplanck, et al.. (2015). The Role of D4Z4-Encoded Proteins in the Osteogenic Differentiation of Mesenchymal Stromal Cells Isolated from Bone Marrow. Stem Cells and Development. 24(22). 2674–2686. 12 indexed citations
7.
Tassin, Alexandra, Baptiste Leroy, Dalila Laoudj‐Chenivesse, et al.. (2012). FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes. PLoS ONE. 7(12). e51865–e51865. 28 indexed citations
8.
Tassin, Alexandra, Dalila Laoudj‐Chenivesse, Céline Vanderplanck, et al.. (2012). DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?. Journal of Cellular and Molecular Medicine. 17(1). 76–89. 117 indexed citations
9.
Dmitriev, Petr, Eugénie Ansseau, Tomas Bos, et al.. (2011). The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy. Journal of Biological Chemistry. 286(52). 44620–44631. 21 indexed citations
10.
Richards, Mark, Frédérique Coppée, Nick Thomas, Alexandra Belayew, & Meena Upadhyaya. (2011). Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?. Human Genetics. 131(3). 325–340. 57 indexed citations
11.
Ansseau, Eugénie, Dalila Laoudj‐Chenivesse, Alexandra Tassin, et al.. (2009). DUX4c Is Up-Regulated in FSHD. It Induces the MYF5 Protein and Human Myoblast Proliferation. PLoS ONE. 4(10). e7482–e7482. 54 indexed citations
12.
Ledent, C., Frédérique Coppée, J.E. Dumont, Gilbert Vassart, & Marc Parmentier. (2009). Transgenic models for proliferative and hyperfunctional thyroid diseases. Experimental and Clinical Endocrinology & Diabetes. 104(S 03). 43–46. 4 indexed citations
13.
Bosnakovski, Darko, Zhaohui Xu, Eun Ji Gang, et al.. (2008). An isogenetic myoblast expression screen identifies DUX4‐mediated FSHD‐associated molecular pathologies. The EMBO Journal. 27(20). 2766–2779. 250 indexed citations
14.
Decaestecker, Christine, O. Filleul, Dominique Chevalier, et al.. (2008). Helicase-like transcription factor exhibits increased expression and altered intracellular distribution during tumor progression in hypopharyngeal and laryngeal squamous cell carcinomas. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 453(5). 491–499. 14 indexed citations
15.
Ansseau, Eugénie, Cecı́lia Conde, Sébastien Sauvage, et al.. (2007). The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein. Neuromuscular Disorders. 17(8). 611–623. 258 indexed citations
16.
Laurent, Sophie, Alain Michel, Frédérique Coppée, et al.. (2006). A New Peptidic Vector for Molecular Imaging of Apoptosis, Identified by Phage Display Technology. SLAS DISCOVERY. 11(5). 537–545. 43 indexed citations
18.
Coppée, Frédérique, et al.. (1998). Differential patterns of cell cycle regulatory proteins expression in transgenic models of thyroid tumours. Oncogene. 17(5). 631–641. 16 indexed citations
19.
Dremier, Sarah, et al.. (1996). Thyroid autonomy: mechanism and clinical effects.. ORBi UMONS. 14 indexed citations
20.
Dumont, J.E., A.M. Ermans, Carine Maenhaut, Frédérique Coppée, & J.B. Stanbury. (1995). Large goitre as a maladaptation to iodine deficiency. Clinical Endocrinology. 43(1). 1–10. 49 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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