Hervé Le Marec

12.5k total citations · 2 hit papers
74 papers, 5.3k citations indexed

About

Hervé Le Marec is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Hervé Le Marec has authored 74 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Cardiology and Cardiovascular Medicine, 45 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Hervé Le Marec's work include Cardiac electrophysiology and arrhythmias (48 papers), Ion channel regulation and function (35 papers) and ECG Monitoring and Analysis (14 papers). Hervé Le Marec is often cited by papers focused on Cardiac electrophysiology and arrhythmias (48 papers), Ion channel regulation and function (35 papers) and ECG Monitoring and Analysis (14 papers). Hervé Le Marec collaborates with scholars based in France, United States and Netherlands. Hervé Le Marec's co-authors include Jean‐Jacques Schott, Vincent Probst, Florence Kyndt, Denis Escande, Flavien Charpentier, Charles Gauthier, Arthur A.M. Wilde, Jean‐Noël Trochu, Dominique Langin and Geneviève Tavernier and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Hervé Le Marec

72 papers receiving 5.1k 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 Peter J. Mohler, Jean‐Jacques Schott et al. profile →
Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome

2010 531 citations Vincent Probst, Christian Veltmann et al. Circulation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hervé Le Marec France	34	4.3k	3.5k	571	502	277	74	5.3k
J. David Port United States	33	2.3k 0.5×	2.7k 0.8×	573 1.0×	426 0.8×	374 1.4×	92	4.6k
Shigeki Kobayashi Japan	35	2.4k 0.6×	2.3k 0.6×	497 0.9×	546 1.1×	268 1.0×	198	4.3k
Harvey S. Hahn United States	28	2.1k 0.5×	2.5k 0.7×	292 0.5×	374 0.7×	267 1.0×	47	3.8k
Flavien Charpentier France	33	2.7k 0.6×	2.6k 0.7×	674 1.2×	226 0.5×	332 1.2×	84	3.7k
Saul Winegrad United States	34	2.6k 0.6×	2.0k 0.6×	506 0.9×	418 0.8×	135 0.5×	74	3.5k
Kathryn A. Yamada United States	41	2.5k 0.6×	3.1k 0.9×	524 0.9×	449 0.9×	363 1.3×	68	4.7k
Håvard Attramadal Norway	31	828 0.2×	2.1k 0.6×	867 1.5×	591 1.2×	278 1.0×	89	3.3k
Beata M. Wolska United States	33	2.4k 0.6×	2.0k 0.6×	280 0.5×	497 1.0×	206 0.7×	87	3.5k
Alicia Mattiazzi Argentina	34	2.3k 0.5×	2.1k 0.6×	448 0.8×	322 0.6×	114 0.4×	113	3.3k
Peter Karczewski Germany	26	1.9k 0.5×	2.2k 0.6×	382 0.7×	274 0.5×	107 0.4×	61	2.8k

Countries citing papers authored by Hervé Le Marec

Since Specialization

Citations

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

Fields of papers citing papers by Hervé Le Marec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hervé Le Marec. 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 Hervé Le Marec. The network helps show where Hervé Le Marec may publish in the future.

Co-authorship network of co-authors of Hervé Le Marec

This figure shows the co-authorship network connecting the top 25 collaborators of Hervé Le Marec. A scholar is included among the top collaborators of Hervé Le Marec 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 Hervé Le Marec. Hervé Le Marec 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

Gourraud, Jean‐Baptiste, Julien Barc, Aurélie Thollet, Hervé Le Marec, & Vincent Probst. (2017). Brugada syndrome: Diagnosis, risk stratification and management. Archives of cardiovascular diseases. 110(3). 188–195. 47 indexed citations

Wieneke, Heinrich, Domenico Corrado, Jeff Lande, et al.. (2015). THE ROLE OF GENETICS IN VENTRICULAR TACHYARRHYTHMIA RISK STRATIFICATION: PRIMARY RESULTS FROM THE DISCOVERY TRIAL. Journal of the American College of Cardiology. 65(10). A270–A270. 1 indexed citations

Gourraud, Jean‐Baptiste, Solena Le Scouarnec, Frédéric Sacher, et al.. (2013). Identification of Large Families in Early Repolarization Syndrome. Journal of the American College of Cardiology. 61(2). 164–172. 52 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

Probst, Vincent, Christian Veltmann, Lars Eckardt, et al.. (2010). Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome. Circulation. 121(5). 635–643. 531 indexed citations breakdown →

Léoni, Anne‐Laure, Bruno Gavillet, Jean‐Sébastien Rougier, et al.. (2010). Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model. PLoS ONE. 5(2). e9298–e9298. 57 indexed citations

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

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

Scouarnec, Solena Le, Naina Bhasin, Thomas J. Hund, et al.. (2008). Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease. Proceedings of the National Academy of Sciences. 105(40). 15617–15622. 109 indexed citations

10.

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

11.

Probst, Vincent, Solena Le Scouarnec, Pierre Boisseau, et al.. (2006). P4-2. Heart Rhythm. 3(5). S219–S219. 1 indexed citations

12.

Probst, Vincent, et al.. (2005). Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation. The American Journal of Cardiology. 95(5). 700–702. 22 indexed citations

13.

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

14.

André-Fouët, Xavier, Jérôme Duisit, Nicolas Costes, et al.. (2003). Cardiac retention of [¹¹C]HED in genotyped long QT patients: a potential amplifier role for severity of the disease. American Journal of Physiology-Heart and Circulatory Physiology. 285(3). H1286–H1293. 18 indexed citations

15.

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

16.

Probst, Vincent, et al.. (2000). Electropharmacological characterization of cardiac repolarization in German shepherd dogs with an inherited syndrome of sudden death: abnormal response to potassium channel blockers. Journal of the American College of Cardiology. 36(3). 939–947. 13 indexed citations

17.

Lande, Gilles, et al.. (1998). Do inherited prothrombotic factors have a role in myocardial infarction with normal coronary arteriogram?. Journal of Internal Medicine. 244(6). 543–544. 14 indexed citations

18.

Gauthier, Charles, Véronique Leblais, Lester Kobzik, et al.. (1998). The negative inotropic effect of beta3-adrenoceptor stimulation is mediated by activation of a nitric oxide synthase pathway in human ventricle.. Journal of Clinical Investigation. 102(7). 1377–1384. 303 indexed citations

19.

Drouin, Emmanuel, Flavien Charpentier, Chantal Gauthier, Karine Laurent, & Hervé Le Marec. (1995). Electrophysiologic characteristics of cells spanning the left ventricular wall of human heart: Evidence for presence of M cells. Journal of the American College of Cardiology. 26(1). 185–192. 286 indexed citations

20.

Gauthier, Chantal, et al.. (1994). Endomyocardial Biopsies: A New Approach for Studying the Electrical and Mechanical Properties of Human Ventricular Myocardium. Journal of Molecular and Cellular Cardiology. 26(10). 1267–1271. 13 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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