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

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

#	Work	Indexed citations
1	Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome 2024 ·Heart Rhythm ·(unknown), Virginnio Proost, Aurélie Thollet, Julien Barc, Alexander J. Groffen, Christiaan C. Veerman, Saskia N. van der Crabben, (unknown), Florence Kyndt, Sean J. Jurgens, Michael W.T. Tanck, Pieter G. Postema, J. Peter van Tintelen, Connie R. Bezzina, Vincent Probst, Arthur A.M. Wilde, Jean‐Baptiste Gourraud, Ahmad S. Amin	2
2	Familial Screening in Case of Acute Myocarditis Reveals Inherited Arrhythmogenic Left Ventricular Cardiomyopathies 2020 ·ESC Heart Failure ·Nicolas Piriou, (unknown), Florence Kyndt, Jean Michel Serfaty, Claire Toquet, Laurianne Le Gloan, Karine Warin‐Fresse, (unknown), Thierry Le Tourneau, (unknown), Aurélie Thollet, Vincent Probst, Jean‐Noël Trochu	49
3	Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndrome 2019 ·Archives of cardiovascular diseases ·Marine Arnaud, (unknown), Romain Tixier, Jean Paul Briand, (unknown), (unknown), Dominique Babuty, Jacques Mansourati, Laurence Jesel, Jean‐Marc Dupuis, Paul Bru, Florence Kyndt, Béatrice Guyomarch, Aurélie Thollet, Nathalie Béhar, Philippe Mabo, Frédéric Sacher, Vincent Probst, Jean‐Baptiste Gourraud	0
4	Clinical presentation and follow-up of women affected by Brugada syndrome 2018 ·Heart Rhythm ·(unknown), Romain Tixier, Jean Paul Briand, (unknown), Dominique Babuty, Jacques Mansourati, Laurence Jesel, Jean‐Marc Dupuis, Paul Bru, Florence Kyndt, Béatrice Guyomarch, Aurélie Thollet, Nathalie Béhar, Philippe Mabo, Frédéric Sacher, Vincent Probst, Jean‐Baptiste Gourraud	16
5	The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway 2017 ·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Pauline Labbé, Emilie Faure, Simon Lecointe, Solena Le Scouarnec, Florence Kyndt, (unknown), Thierry Le Tourneau, Bernard Offmann, Cécile Duplàa, Stéphane Zaffran, Jean‐Jacques Schott, Jean Mérot	14
6	0292: Cardiac phenotype and prognosis of patients with mutations in NKX2.5 gene 2016 ·Archives of Cardiovascular Diseases Supplements ·Philippe Maury, Alban‐Elouen Baruteau, Estelle Gandjbakhch, Francis Bessière, Patrice Bouvagnet, Florence Kyndt, Sébastien Hascoët, (unknown), Françoise Hidden‐Lucet, Philippe Chevalier, Damien Bonnet, Vincent Probst, Alice Maltret	1
7	New description of a family with an autosomal recessive cathecholergic ventricular tachycardia due to Triadin gene 2014 ·Archives of cardiovascular diseases ·Caroline Rooryck, Florence Kyndt, Nathalie Roux-Buisson, Frédéric Sacher, Philippe Ritter, Vincent Probst, Jean‐Benoît Thambo	1
8	0030: ARHGAP 24/ (FilGAP); a new gene responsible for mitral valve prolapse 2014 ·Archives of Cardiovascular Diseases Supplements ·(unknown), Antoine Rimbert, Florence Kyndt, Thierry Le Tourneau, Vincent Probst, Jean‐Jacques Schott, Jean Mérot	1
9	Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation 2013 ·EP Europace ·(unknown), F. Sacher, Philippe Maury, Philippe Mabo, Jacques Mansourati, Isabelle E. Magnin, (unknown), (unknown), (unknown), Florence Kyndt, M. Haïssaguerre, Stéphane Bezieau, Béatrice Guyomarch, Hervé Le Marec, Véronique Fressart, Isabelle Denjoy, Vincent Probst	46
10	187 New findings in mitral valve prolapse related to filamin-A mutations 2012 ·Archives of Cardiovascular Diseases Supplements ·Thierry Le Tourneau, (unknown), Florence Kyndt, Jean Mérot, Albert Hagège, Robert A. Levine, Hervé Le Marec, Jean‐Jacques Schott, Vincent Probst	1
11	Filamin-A-Related Myxomatous Mitral Valve Dystrophy: Genetic, Echocardiographic and Functional Aspects 2011 ·Journal of Cardiovascular Translational Research ·(unknown), Florence Kyndt, Simon Lecointe, Hervé Le Marec, Jean Mérot, Jean‐Jacques Schott, Thierry Le Tourneau, Vincent Probst	38
12	Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome 2010 ·Journal of the American College of Cardiology ·Julien Barc, (unknown), Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, (unknown), Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott	58
13	SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome 2009 ·Circulation Cardiovascular Genetics ·Vincent Probst, Arthur A.M. Wilde, Julien Barc, Frédéric Sacher, Dominique Babuty, Philippe Mabo, Jacques Mansourati, Solena Le Scouarnec, Florence Kyndt, Cédric Le Caignec, Pascale Guicheney, Laëtitia Gouas, Juliette Albuisson, Paola G. Meregalli, Hervé Le Marec, Hanno L. Tan, Jean‐Jacques Schott	211
14	Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges 2009 ·EP Europace ·Christian Veltmann, (unknown), Frédéric Sacher, Philippe Mabo, Rainer Schimpf, Florian Streitner, Joachim Brade, Florence Kyndt, Juergen Kuschyk, (unknown), (unknown), Vincent Probst	55
15	G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome 2009 ·Archives of cardiovascular diseases ·Julien Barc, Vincent Probst, Arthur A.M. Wilde, Frédéric Sacher, Dominique Babuty, Philippe Mabo, Jacques Mansourati, (unknown), Florence Kyndt, Pascale Guicheney, Juliette Albuisson, Paola G. Meregalli, Hervé Le Marec, Hanno L. Tan, Jean‐Jacques Schott	1
16	Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene 2008 ·Prenatal Diagnosis ·Norbert Winer, Florence Kyndt, A. Paumier, A. David, Bertrand Isidor, (unknown), (unknown), (unknown), (unknown), (unknown), Deborah Krakow, Cédric Le Caignec	6
17	[Genetic aspects of valvulopathies]. 2007 ·PubMed ·Florence Kyndt, Solena Le Scouarnec, (unknown), (unknown), Antoine Legendre, Jean‐Noël Trochu, (unknown), André Chaventré, Jean‐Jacques Schott, Hervé Le Marec, Vincent Probst	8
18	Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease 2003 ·Journal of the American College of Cardiology ·Vincent Probst, Florence Kyndt, F Potet, Jean‐Noël Trochu, (unknown), Sophie Demolombe, Jean‐Jacques Schott, Isabelle Baró, Denis Escande, Hervé Le Marec	115
19	Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28 2000 ·Journal of the American College of Cardiology ·Jean‐Noël Trochu, Florence Kyndt, Jean‐Jacques Schott, Jean-Pierre Gueffet, Vincent Probst, Bernard Bénichou, Hervé Le Marec	33
20	Mutations in a Dominant-Negative Isoform Correlate with Phenotype in Inherited Cardiac Arrhythmias 1999 ·The American Journal of Human Genetics ·Raha Mohammad-Panah, Sophie Demolombe, Nathalie Neyroud, Pascale Guicheney, Florence Kyndt, Maurice J.B. van den Hoff, Isabelle Baró, Denis Escande	53

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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