Pascale Sébillon

821 total citations
10 papers, 628 citations indexed

About

Pascale Sébillon is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Pascale Sébillon has authored 10 papers receiving a total of 628 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in Pascale Sébillon's work include Cardiomyopathy and Myosin Studies (4 papers), RNA Research and Splicing (3 papers) and Nuclear Structure and Function (3 papers). Pascale Sébillon is often cited by papers focused on Cardiomyopathy and Myosin Studies (4 papers), RNA Research and Splicing (3 papers) and Nuclear Structure and Function (3 papers). Pascale Sébillon collaborates with scholars based in France, United States and Netherlands. Pascale Sébillon's co-authors include Isabelle Denjoy, Theo M. Hoorntje, Antoine Da Costa, Marcel M. A. M. Mannens, Pascale Guicheney, Jean‐Marc Lupoglazoff, Arthur A.M. Wilde, Alex V. Postma, Michel Komajda and Jeanne Flavigny and has published in prestigious journals such as Nucleic Acids Research, Journal of Molecular Biology and Circulation Research.

In The Last Decade

Pascale Sébillon

10 papers receiving 612 citations

Peers

Pascale Sébillon
L. Demay France
Evgeny Loukianov United States
Tatsuhito Nouchi Japan
A. Ya. Gudkova Russia
Xavière Lornage France
Carola Hedberg Sweden
Julian Schröter Germany
William Wallefeld Australia
S. White Australia
Emily Hanson United States
L. Demay France
Pascale Sébillon
Citations per year, relative to Pascale Sébillon Pascale Sébillon (= 1×) peers L. Demay

Countries citing papers authored by Pascale Sébillon

Since Specialization
Citations

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

Fields of papers citing papers by Pascale Sébillon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascale Sébillon

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

All Works

10 of 10 papers shown
1.
Laforêt, Pascal, Philippe Charron, Thierry Maisonobe, et al.. (2004). Charcot–Marie–Tooth features and maculopathy in a patient with Danon disease. Neurology. 63(8). 1535–1535. 16 indexed citations
2.
Sylvius, Nicolas, Laëtitia Duboscq-Bidot, Christiane Bouchier, et al.. (2003). Mutational analysis of the β‐ and δ‐sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy. American Journal of Medical Genetics Part A. 120A(1). 8–12. 21 indexed citations
3.
Charniot, Jean‐Christophe, Cécile Pascal, Christiane Bouchier, et al.. (2003). Functional consequences of anLMNAmutation associated with a new cardiac and non-cardiac phenotype. Human Mutation. 21(5). 473–481. 57 indexed citations
4.
Sébillon, Pascale, et al.. (2003). Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. Journal of Medical Genetics. 40(8). 560–567. 129 indexed citations
5.
Postma, Alex V., Isabelle Denjoy, Theo M. Hoorntje, et al.. (2002). Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation Research. 91(8). e21–6. 302 indexed citations
6.
Sébillon, Pascale, Gisèle Bonne, Jeanne Flavigny, et al.. (2001). COOH-terminal truncated human cardiac MyBP-C alters myosin filament organization. Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie. 324(3). 251–260. 12 indexed citations
7.
Flavigny, Jeanne, Michel Souchet, Pascale Sébillon, et al.. (1999). COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes. Journal of Molecular Biology. 294(2). 443–456. 58 indexed citations
8.
9.
Bienvenu, Thierry, et al.. (1992). Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification.. PubMed. 64(1). 107–13. 5 indexed citations
10.
Sébillon, Pascale, Thierry Bienvenu, Robert Girot, et al.. (1991). Detection of the Most Frequent β-Thalassemic Defect in Southeast Asia by PCR. Hemoglobin. 15(4). 313–315. 5 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by L. Demay Breakdown of academic impact, for papers by Evgeny Loukianov Breakdown of academic impact, for papers by Tatsuhito Nouchi Breakdown of academic impact, for papers by A. Ya. Gudkova Breakdown of academic impact, for papers by Xavière Lornage Breakdown of academic impact, for papers by Carola Hedberg Breakdown of academic impact, for papers by Julian Schröter Breakdown of academic impact, for papers by William Wallefeld Breakdown of academic impact, for papers by S. White Breakdown of academic impact, for papers by Emily Hanson
Rankless by CCL
2026