Nathalie Neyroud

2.7k total citations · 1 hit paper
34 papers, 1.9k citations indexed

About

Nathalie Neyroud is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nathalie Neyroud has authored 34 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Cardiology and Cardiovascular Medicine, 25 papers in Molecular Biology and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nathalie Neyroud's work include Cardiac electrophysiology and arrhythmias (29 papers), Ion channel regulation and function (21 papers) and Cardiomyopathy and Myosin Studies (6 papers). Nathalie Neyroud is often cited by papers focused on Cardiac electrophysiology and arrhythmias (29 papers), Ion channel regulation and function (21 papers) and Cardiomyopathy and Myosin Studies (6 papers). Nathalie Neyroud collaborates with scholars based in France, United States and Switzerland. Nathalie Neyroud's co-authors include Pascale Guicheney, Isabelle Denjoy, P Coumel, Claire Donger, Ketty Schwartz, Françoise Gary, Christine Petit, Michel Leibovici, Sabine Fauré and Frédérique Tesson and has published in prestigious journals such as Circulation, Nature Genetics and PLoS ONE.

In The Last Decade

Nathalie Neyroud

33 papers receiving 1.9k 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.

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1997 659 citations Nathalie Neyroud, Frédérique Tesson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nathalie Neyroud France	18	1.6k	1.6k	379	199	68	34	1.9k
Claire Donger France	10	1.1k 0.7×	916 0.6×	220 0.6×	190 1.0×	61 0.9×	10	1.4k
Thomas H. Rhodes United States	14	1.4k 0.9×	923 0.6×	718 1.9×	42 0.2×	191 2.8×	15	1.9k
Mirella Memmi Italy	19	3.1k 1.9×	3.9k 2.5×	524 1.4×	75 0.4×	83 1.2×	33	4.2k
Dirk Heitzmann Germany	16	864 0.5×	291 0.2×	161 0.4×	46 0.2×	73 1.1×	25	1.2k
Bratislav M. Velimirovic United States	9	1.0k 0.6×	522 0.3×	620 1.6×	35 0.2×	15 0.2×	11	1.2k
Christian Biervert Germany	9	935 0.6×	470 0.3×	750 2.0×	34 0.2×	167 2.5×	9	1.2k
Stefanie Fenske Germany	15	409 0.3×	218 0.1×	207 0.5×	159 0.8×	33 0.5×	23	816
Syevda Sirenko United States	20	777 0.5×	959 0.6×	284 0.7×	42 0.2×	11 0.2×	36	1.2k
Hongwei Cheng United Kingdom	15	327 0.2×	251 0.2×	141 0.4×	111 0.6×	32 0.5×	33	573
Bettina Linck Germany	19	869 0.5×	711 0.5×	227 0.6×	25 0.1×	21 0.3×	31	1.2k

Countries citing papers authored by Nathalie Neyroud

Since Specialization

Citations

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

Fields of papers citing papers by Nathalie Neyroud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Neyroud

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Neyroud. A scholar is included among the top collaborators of Nathalie Neyroud 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 Nathalie Neyroud. Nathalie Neyroud 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

Doisne, Nicolas, et al.. (2021). In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant. Frontiers in Physiology. 12. 661413–661413. 9 indexed citations

Doisne, Nicolas, Victor Waldmann, Alban Redheuil, et al.. (2020). A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions. Human Mutation. 41(4). 850–859. 22 indexed citations

Clatot, Jérôme, Sabine Duchatelet, Estelle Gandjbakhch, et al.. (2014). A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation. Heart Rhythm. 11(6). 1015–1023. 37 indexed citations

Clatot, Jérôme, Sabine Duchatelet, Estelle Gandjbakhch, et al.. (2013). Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation. Heart Rhythm. 10(11). 1746–1746. 2 indexed citations

Vite, Alexia, Estelle Gandjbakhch, Cathérine Prost, et al.. (2013). Desmosomal Cadherins Are Decreased in Explanted Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patient Hearts. PLoS ONE. 8(9). e75082–e75082. 22 indexed citations

Clatot, Jérôme, Svetlana Maugenre, Isabelle Denjoy, et al.. (2012). Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits. Cardiovascular Research. 96(1). 53–63. 78 indexed citations

Maugenre, Svetlana, Nathalie Neyroud, Elise Balse, et al.. (2011). MOG1. Circulation Cardiovascular Genetics. 4(3). 261–268. 114 indexed citations

El-Haou, Saïd, Elise Balse, Nathalie Neyroud, et al.. (2009). Kv4 Potassium Channels Form a Tripartite Complex With the Anchoring Protein SAP97 and CaMKII in Cardiac Myocytes. Circulation Research. 104(6). 758–769. 66 indexed citations

Maugenre, Svetlana, Nathalie Neyroud, Guillaume Duthoit, et al.. (2009). Abstract 2713: MOG1 Mutations Associated With Brugada Syndrome Electrocardiogram Pattern. Circulation. 120. 1 indexed citations

10.

El-Haou, Saïd, Elise Balse, Nathalie Neyroud, et al.. (2008). The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes. American Journal of Physiology-Heart and Circulatory Physiology. 294(4). H1851–H1861. 39 indexed citations

11.

Duboscq-Bidot, Laëtitia, Peng Xu, Philippe Charron, et al.. (2007). Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy. Cardiovascular Research. 77(1). 118–125. 76 indexed citations

12.

Neyroud, Nathalie, et al.. (2004). Les MAGUK : au-delà de l’accrochage des canaux ioniques. médecine/sciences. 20(1). 84–88. 3 indexed citations

13.

Neyroud, Nathalie, et al.. (2004). Les MAGUK : au-delà de l’accrochage des canaux ioniques. médecine/sciences. 20(1). 84–88. 3 indexed citations

14.

Neyroud, Nathalie, Isabelle Deschênes, Masaharu Akao, Hanne Nuss, & Eduardo Marbán. (2002). Somatic Gene Transfer of Tagged K+ Channel Fragments to Probe Trafficking and Electrical Function in Epithelial Cells and Cardiac Myocytes. The Journal of Membrane Biology. 190(2). 133–144. 3 indexed citations

15.

Neyroud, Nathalie, Hanne Nuss, Michelle K. Leppo, Eduardo Marbán, & J. Kevin Donahue. (2002). [19] Gene delivery to cardiac muscle. Methods in enzymology on CD-ROM/Methods in enzymology. 346. 323–334. 4 indexed citations

16.

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

17.

Extramiana, Fabrice, Nathalie Neyroud, Heikki V. Huikuri, et al.. (1999). QT interval and arrhythmic risk assessment after myocardial infarction. The American Journal of Cardiology. 83(2). 266–269. 39 indexed citations

18.

Neyroud, Nathalie, Isabelle Denjoy, Claire Donger, et al.. (1998). Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome. European Journal of Human Genetics. 6(2). 129–133. 35 indexed citations

19.

Neyroud, Nathalie, Frédérique Tesson, Isabelle Denjoy, et al.. (1997). A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genetics. 15(2). 186–189. 659 indexed citations breakdown →

20.

Coumel, P, et al.. (1995). Different circadian behavior of the apex and the end of the T wave. Journal of Electrocardiology. 28. 138–142. 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.

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