| 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, C Donger, J Barhanin, ... Nature genetics 15 (2), 186-189, 1997 | 1095 | 1997 |
| KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome C Donger, I Denjoy, M Berthet, N Neyroud, C Cruaud, M Bennaceur, ... Circulation 96 (9), 2778-2781, 1997 | 481 | 1997 |
| 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, G Romey, ... The EMBO journal, 1997 | 350 | 1997 |
| MOG1 A New Susceptibility Gene for Brugada Syndrome D Kattygnarath, S Maugenre, N Neyroud, E Balse, C Ichai, I Denjoy, ... Circulation: Cardiovascular Genetics 4 (3), 261-268, 2011 | 198 | 2011 |
| Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin I Deschênes, N Neyroud, D DiSilvestre, E Marbán, DT Yue, ... Circulation research 90 (4), e49-e57, 2002 | 186 | 2002 |
| 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, I Denjoy, L Demay, ... Circulation research 84 (3), 290-297, 1999 | 148 | 1999 |
| Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk C Chouabe, N Neyroud, P Richard, I Denjoy, B Hainque, G Romey, ... Cardiovascular research 45 (4), 971-980, 2000 | 141 | 2000 |
| Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 (HERG) Mutations JM Lupoglazoff, I Denjoy, M Berthet, N Neyroud, L Demay, P Richard, ... Circulation 103 (8), 1095-1101, 2001 | 131 | 2001 |
| Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy L Duboscq-Bidot, P Xu, P Charron, N Neyroud, G Dilanian, A Millaire, ... Cardiovascular research 77 (1), 118-125, 2008 | 130 | 2008 |
| Kv4 potassium channels form a tripartite complex with the anchoring protein SAP97 and CaMKII in cardiac myocytes S El-Haou, E Balse, N Neyroud, G Dilanian, B Gavillet, H Abriel, ... Circulation research 104 (6), 758-769, 2009 | 113 | 2009 |
| Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits J Clatot, A Ziyadeh-Isleem, S Maugenre, I Denjoy, H Liu, G Dilanian, ... Cardiovascular research 96 (1), 53-63, 2012 | 112 | 2012 |
| Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome N Neyroud, P Maison-Blanche, I Denjoy, S Chevret, C Donger, E Dausse, ... European heart journal 19 (1), 158-165, 1998 | 107 | 1998 |
| QT interval and arrhythmic risk assessment after myocardial infarction F Extramiana, N Neyroud, HV Huikuri, MJ Koistinen, P Coumel, ... American Journal of Cardiology 83 (2), 266-269, 1999 | 82 | 1999 |
| Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias R Mohammad-Panah, S Demolombe, N Neyroud, P Guicheney, F Kyndt, ... The American Journal of Human Genetics 64 (4), 1015-1023, 1999 | 79 | 1999 |
| A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation A Ziyadeh-Isleem, J Clatot, S Duchatelet, E Gandjbakhch, I Denjoy, ... Heart Rhythm 11 (6), 1015-1023, 2014 | 66 | 2014 |
| Splicing Mutations in KCNQ1 A Mutation Hot Spot at Codon 344 That Produces In Frame Transcripts A Murray, C Donger, C Fenske, I Spillman, P Richard, YB Dong, ... Circulation 100 (10), 1077-1084, 1999 | 63 | 1999 |
| The anchoring protein SAP97 retains Kv1. 5 channels in the plasma membrane of cardiac myocytes J Abi-Char, S El-Haou, E Balse, N Neyroud, R Vranckx, A Coulombe, ... American Journal of Physiology-Heart and Circulatory Physiology 294 (4 …, 2008 | 61 | 2008 |
| 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, E Villain, A Leenhardt, K Benali, ... European Journal of Human Genetics 6 (2), 129-133, 1998 | 51 | 1998 |
| Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts A Vite, E Gandjbakhch, C Prost, V Fressart, P Fouret, N Neyroud, F Gary, ... PloS one 8 (9), e75082, 2013 | 32 | 2013 |
| A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions N Doisne, V Waldmann, A Redheuil, X Waintraub, V Fressart, F Ader, ... Human Mutation 41 (4), 850-859, 2020 | 27 | 2020 |