Florence Kyndt

7.1k total citations · 1 hit paper
45 papers, 2.7k citations indexed

About

Florence Kyndt is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Florence Kyndt has authored 45 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Cardiology and Cardiovascular Medicine, 25 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Florence Kyndt's work include Cardiac electrophysiology and arrhythmias (26 papers), Ion channel regulation and function (17 papers) and Cardiomyopathy and Myosin Studies (11 papers). Florence Kyndt is often cited by papers focused on Cardiac electrophysiology and arrhythmias (26 papers), Ion channel regulation and function (17 papers) and Cardiomyopathy and Myosin Studies (11 papers). Florence Kyndt collaborates with scholars based in France, Netherlands and United States. Florence Kyndt's co-authors include Jean‐Jacques Schott, Hervé Le Marec, Vincent Probst, Denis Escande, Arthur A.M. Wilde, Vann Bennett, Peter J. Mohler, Sílvia Guatimosim, W. Jonathan Lederer and Anthony O. Gramolini and has published in prestigious journals such as Nature, Circulation and Nature Genetics.

In The Last Decade

Florence Kyndt

42 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

2003 693 citations Jean‐Jacques Schott, Florence Kyndt et al. profile →

Peers

Florence Kyndt

CCM

CMN

SURGE

GENET

Matteo Vatta United States

Ana Morales United States

Duanxiang Li United States

Jonathan T. Lu United States

Gianina Ravenscroft Australia

S. Kubalak United States

David Y. Barefield United States

Daniel J. Lerner United States

Angela deAlmeida United States

Susana Quijano-Roy France

Matteo Vatta United States

Florence Kyndt

2.0k ×0.8

CCM

1.4k ×0.7

150 ×0.6

CMN

137 ×0.9

SURGE

148 ×1.0

GENET

Citations per year, relative to Florence Kyndt Florence Kyndt (= 1×) peers Matteo Vatta

Countries citing papers authored by Florence Kyndt

Since Specialization

Citations

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

Fields of papers citing papers by Florence Kyndt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Kyndt

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

All Works

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20 of 20 papers shown

Proost, Virginnio, Aurélie Thollet, Julien Barc, et al.. (2024). Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome. Heart Rhythm. 22(5). 1321–1329. 2 indexed citations

Piriou, Nicolas, Florence Kyndt, Jean Michel Serfaty, et al.. (2020). Familial Screening in Case of Acute Myocarditis Reveals Inherited Arrhythmogenic Left Ventricular Cardiomyopathies. ESC Heart Failure. 7(4). 1520–1533. 49 indexed citations

Arnaud, Marine, Romain Tixier, Jean Paul Briand, et al.. (2019). Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndrome. Archives of cardiovascular diseases. 113(3). 152–158.

Tixier, Romain, Jean Paul Briand, Dominique Babuty, et al.. (2018). Clinical presentation and follow-up of women affected by Brugada syndrome. Heart Rhythm. 16(2). 260–267. 16 indexed citations

Labbé, Pauline, Emilie Faure, Simon Lecointe, et al.. (2017). The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1864(7). 1142–1152. 14 indexed citations

Maury, Philippe, Alban‐Elouen Baruteau, Estelle Gandjbakhch, et al.. (2016). 0292: Cardiac phenotype and prognosis of patients with mutations in NKX2.5 gene. Archives of Cardiovascular Diseases Supplements. 8(1). 100–100. 1 indexed citations

Rooryck, Caroline, Florence Kyndt, Nathalie Roux-Buisson, et al.. (2014). New description of a family with an autosomal recessive cathecholergic ventricular tachycardia due to Triadin gene. Archives of cardiovascular diseases. 107(8-9). 496–496. 1 indexed citations

Rimbert, Antoine, Florence Kyndt, Thierry Le Tourneau, et al.. (2014). 0030: ARHGAP 24/ (FilGAP); a new gene responsible for mitral valve prolapse. Archives of Cardiovascular Diseases Supplements. 6. 72–73. 1 indexed citations

Sacher, F., Philippe Maury, Philippe Mabo, et al.. (2013). Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation. EP Europace. 15(12). 1805–1811. 46 indexed citations

10.

Tourneau, Thierry Le, Florence Kyndt, Jean Mérot, et al.. (2012). 187 New findings in mitral valve prolapse related to filamin-A mutations. Archives of Cardiovascular Diseases Supplements. 4(1). 59–59. 1 indexed citations

11.

Kyndt, Florence, Simon Lecointe, Hervé Le Marec, et al.. (2011). Filamin-A-Related Myxomatous Mitral Valve Dystrophy: Genetic, Echocardiographic and Functional Aspects. Journal of Cardiovascular Translational Research. 4(6). 748–756. 38 indexed citations

12.

Barc, Julien, Sébastien Schmitt, Florence Kyndt, et al.. (2010). Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome. Journal of the American College of Cardiology. 57(1). 40–47. 58 indexed citations

13.

Probst, Vincent, Arthur A.M. Wilde, Julien Barc, et al.. (2009). SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome. Circulation Cardiovascular Genetics. 2(6). 552–557. 211 indexed citations

14.

Veltmann, Christian, Frédéric Sacher, Philippe Mabo, et al.. (2009). Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges. EP Europace. 11(10). 1345–1352. 55 indexed citations

15.

Barc, Julien, Vincent Probst, Arthur A.M. Wilde, et al.. (2009). G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome. Archives of cardiovascular diseases. 102. S70–S70. 1 indexed citations

16.

Winer, Norbert, Florence Kyndt, A. Paumier, et al.. (2008). Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene. Prenatal Diagnosis. 29(2). 172–174. 6 indexed citations

17.

Kyndt, Florence, Solena Le Scouarnec, Antoine Legendre, et al.. (2007). [Genetic aspects of valvulopathies].. PubMed. 100(12). 1013–20. 8 indexed citations

18.

Probst, Vincent, Florence Kyndt, F Potet, et al.. (2003). Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease. Journal of the American College of Cardiology. 41(4). 643–652. 115 indexed citations

19.

Trochu, Jean‐Noël, Florence Kyndt, Jean‐Jacques Schott, et al.. (2000). Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28. Journal of the American College of Cardiology. 35(7). 1890–1897. 33 indexed citations

20.

Mohammad-Panah, Raha, Sophie Demolombe, Nathalie Neyroud, et al.. (1999). Mutations in a Dominant-Negative Isoform Correlate with Phenotype in Inherited Cardiac Arrhythmias. The American Journal of Human Genetics. 64(4). 1015–1023. 53 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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