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N. Neyroud · SciRah

Researcher profile · Semantic Scholar

N. Neyroud

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N. Neyroud — researcher profile on SciRah

h-index: 20
Works: 62
Citations: 3,168

Most-cited papers

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
N. Neyroud, F. Tesson, I. Denjoy, M. Leibovici +8 more
1997Nature Genetics907 citations
Semantic Scholar
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.
C. Donger, I. Denjoy, M. Berthet, N. Neyroud +6 more
1997Circulation330 citations
Semantic Scholar
Properties of KvLQT1 K+ channel mutations in Romano–Ward and Jervell and Lange‐Nielsen inherited cardiac arrhythmias
C. Chouabe, N. Neyroud, P. Guicheney, M. Lazdunski +2 more
1997EMBO Journal310 citations Open access
Semantic Scholar
MOG1: A New Susceptibility Gene for Brugada Syndrome
D. Kattygnarath, Svetlana Maugenre, N. Neyroud, E. Balse +14 more
2011Circulation: Cardiovascular Genetics171 citations Open access
Semantic Scholar
Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin
I. Deschênes, N. Neyroud, D. DiSilvestre, E. Marbán +2 more
2002Circulation Research167 citations
Semantic Scholar
Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk.
C. Chouabe, N. Neyroud, P. Richard, I. Denjoy +5 more
2000Cardiovascular Research126 citations Open access
Semantic Scholar
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.
N. Neyroud, P. Richard, N. Vignier, C. Donger +9 more
1999Circulation Research122 citations
Semantic Scholar
Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 (HERG) Mutations
J. Lupoglazoff, I. Denjoy, M. Berthet, N. Neyroud +9 more
2001Circulation110 citations Open access
Semantic Scholar
Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.
L. Duboscq-Bidot, P. Xu, P. Charron, N. Neyroud +5 more
2008Cardiovascular Research108 citations
Semantic Scholar
Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits.
Jérôme Clatot, A. Ziyadeh-Isleem, Svetlana Maugenre, I. Denjoy +7 more
2012Cardiovascular Research101 citations Open access
Semantic Scholar
Kv4 Potassium Channels Form a Tripartite Complex With the Anchoring Protein SAP97 and CaMKII in Cardiac Myocytes
Said El-Haou, E. Balse, N. Neyroud, G. Dilanian +5 more
2009Circulation Research96 citations Open access
Semantic Scholar
Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.
N. Neyroud, P. Maison-Blanche, I. Denjoy, S. Chevret +8 more
1998European Heart Journal91 citations
Semantic Scholar
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.
R. Mohammad-Panah, S. Demolombe, N. Neyroud, P. Guicheney +4 more
1999American Journal of Human Genetics80 citations Open access
Semantic Scholar
The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes.
J. Abi-Char, Said El-Haou, E. Balse, N. Neyroud +3 more
2008American Journal of Physiology. Heart and Circulatory Physiology59 citations Open access
Semantic Scholar
Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcripts.
A. Murray, C. Donger, C. Fenske, I. Spillman +11 more
1999Circulation54 citations
Semantic Scholar
QT interval and arrhythmic risk assessment after myocardial infarction.
F. Extramiana, N. Neyroud, H. Huikuri, M. Koistinen +2 more
1999American Journal of Cardiology52 citations
Semantic Scholar
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome
N. Neyroud, I. Denjoy, C. Donger, F. Gary +6 more
1998European Journal of Human Genetics48 citations
Semantic Scholar
A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation
A. Ziyadeh-Isleem, Jérôme Clatot, S. Duchatelet, E. Gandjbakhch +7 more
2014Heart Rhythm47 citations Open access
Semantic Scholar
A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions
N. Doisne, Victor Waldmann, alban redheuil, X. Waintraub +6 more
2020Human Mutation30 citations
Semantic Scholar
Desmosomal Cadherins Are Decreased in Explanted Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patient Hearts
A. Vite, E. Gandjbakhch, C. Prost, V. Fressart +11 more
2013PLoS ONE29 citations Open access
Semantic Scholar
[Ventricular repolarization and Holter monitoring. Effect of sympathetic blockage on the QT/RR ratio].
F. Extramiana, R. Tavernier, P. Maison-Blanche, N. Neyroud +3 more
2000Archives des maladies du coeur et des vaisseaux20 citations
Semantic Scholar
Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies
Jérôme Clatot, N. Neyroud, R. Cox, Charlotte Souil +3 more
2020International Journal of Molecular Sciences18 citations Open access
Semantic Scholar
Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers.
F. Extramiana, I. Denjoy, F. Badilini, Iheb Chabani +8 more
2005American Journal of Cardiology17 citations
Semantic Scholar
In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant
N. Doisne, M. Grauso, N. Mougenot, M. Clergue +4 more
2021Frontiers in Physiology16 citations Open access
Semantic Scholar
Gene delivery to cardiac muscle.
N. Neyroud, H. Nuss, Michelle K. Leppo, E. Marbán +1 more
2002Methods in Enzymology9 citations
Semantic Scholar
P5713A new scn5a mutation responsible for multifocal ectopic purkinje-related premature contractions
N. Doisne, Victor Waldmann, X. Waintraub, V. Fressart +5 more
2018European Heart Journal8 citations
Semantic Scholar
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response
M. Blancard, Zahia Touat-Hamici, Yuriana Aguilar-Sánchez, L. Yin +9 more
2021Journal of Personalized Medicine7 citations Open access
Semantic Scholar
Different circadian behavior of the apex and the end of the T wave.
P. Coumel, P. Maison-Blanche, D. Catuli, N. Neyroud +2 more
1995Journal of Electrocardiology7 citations
Semantic Scholar
Abstract 2713: MOG1 Mutations Associated With Brugada Syndrome Electrocardiogram Pattern
D. Kattygnarath, Svetlana Maugenre, N. Neyroud, G. Duthoit +7 more
20095 citations
Semantic Scholar
Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa.
Jérôme Clatot, A. Coulombe, I. Deschênes, P. Guicheney +1 more
2022Frontiers in Bioscience4 citations Open access
Semantic Scholar
[Congenital long QT syndrome. The value of genetics in prognostic evaluation].
I. Denjoy, J. Lupoglazoff, C. Donger, M. Berthet +6 more
1999Archives des maladies du coeur et des vaisseaux4 citations
Semantic Scholar
807 Heart rate influences on repolarization duration and morphology in symptomatic and asymptomatic KCNQ1 mutation carriers
F. Extramiana, I. Denjoy, N. Neyroud, P. Guicheney +3 more
20053 citations Open access
Semantic Scholar
[MAGUKs: beyond ionic channel anchoring].
D. Godreau, N. Neyroud, R. Vranckx, S. Hatem
2004Medecine sciences : M/S3 citations Open access
Semantic Scholar
Somatic Gene Transfer of Tagged K+ Channel Fragments to Probe Trafficking and Electrical Function in Epithelial Cells and Cardiac Myocytes
N. Neyroud, I. Deschênes, M. Akao, H. Nuss +1 more
2002Journal of Membrane Biology3 citations
Semantic Scholar
P371Role of the N- and distal C-terminal domains in Nav1.5 alpha-subunit interaction
N. Neyroud, A. Ziyadeh-Isleem, Jérôme Clatot, I. Deschênes +2 more
20142 citations Open access
Semantic Scholar
Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation
Jérôme Clatot, A. Ziyadeh-Isleem, S. Duchatelet, E. Gandjbakhch +7 more
20132 citations
Semantic Scholar
Properties of KvLQT 1 K channel mutations in Romano – Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias are not a frequent diagnosis , acquired forms of abnormal
C. Chouabe, N. Neyroud, P. Guicheney, M. Lazdunski
20131 citations
Semantic Scholar
Faculty Opinions recommendation of Interactions between ankyrin-G, Plakophilin-2, and Connexin43 at the cardiac intercalated disc.
P. Guicheney, N. Neyroud
20111 citations Open access
Semantic Scholar
The Anchoring Protein SAP97 Is Crucial For The Surface Expression Of Shal Kv Potassium Channels And Their Regulation By CaMKII In Cardiac Myocytes
Said El-Haou, E. Balse, N. Neyroud, B. Gavillet +4 more
20091 citations Open access
Semantic Scholar
Repolarisation ventriculaire et enregistrement Holter: Rôle du blocage sympathique sur la physiologie de la relation QT/RR
F. Extramiana, R. Tavernier, P. Maison-Blanche, N. Neyroud +3 more
20001 citations
Semantic Scholar
Abstract 17871: Heterozygous Carriers of KCNQ1 Variants Associated With the Jervell-Lange-Nielsen Syndrome Have a Better Outcome When Compared to Other Type 1 LQTS Patients
C. Morgat, I. Denjoy, V. Fressart, N. Neyroud +7 more
2023Circulation0 citations
Semantic Scholar
Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition.
M. Gizon, L. Duboscq-Bidot, Lina El Kassar, P. Bobin +6 more
2022Stem Cell Research0 citations Open access
Semantic Scholar
CRISPR/Cas9-mediated generation of cardiomyocytes derived from human induced pluripotent stem cells to model SCN5A deficiency
M. Gizon, V. Fontaine, L. Duboscq-Bidot, L. El Kassa +3 more
20210 citations Open access
Semantic Scholar
A new SCN5A mutation responsible for Multifocal Ectopic Purkinje-Related Premature Contractions
N. Doisne, Victor Waldmann, V. Fressart, alban redheuil +5 more
2019Archives of Cardiovascular Diseases Supplements0 citations Open access
Semantic Scholar
P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs
N. Doisne, M. Grauso-Culetto, N. Mougenot, M. Clergue +5 more
20180 citations
Semantic Scholar
Overexpression of the cardiac Na + channel in Scn5a deficient mice using AAVs
N. Doisne, M. Grauso, N. Mougenot, M. Clergue +4 more
20170 citations Open access
Semantic Scholar
Modeling susceptibility to drug-induced long qt syndrome with a panel of subject-specific induced pluripotent stem cells
M. Grauso, N. Mougenot, M. Clergue, A. Coulombe +10 more
20160 citations
Semantic Scholar
0151 : In vivo modulation of the cardiac Na+ current using AAVs
N. Doisne, M. Grauso, N. Mougenot, M. Clergue +3 more
20160 citations Open access
Semantic Scholar
0235 : In vivo overexpression of a cardiac sodium channel mutant in mice
N. Doisne, M. Grauso, N. Mougenot, M. Clergue +3 more
20150 citations Open access
Semantic Scholar
Faculty Opinions recommendation of Divergent regulation of ryanodine receptor 2 calcium release channels by arrhythmogenic human calmodulin missense mutants.
P. Guicheney, N. Neyroud
20140 citations Open access
Semantic Scholar

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A. Coulombe×16
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