Nathalie Neyroud

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

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al. · Nature Genetics · 1997 · 881 citations

Novel Mutation, Channelopathies, Cardiomyopathy +10

<i>KVLQT1</i> C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

Claire Donger, Isabelle Denjoy, Myriam Berthet et al. · Circulation · 1997 · 346 citations

<i>MOG1</i>

Darouna Kattygnarath, Svetlana Maugenre, Nathalie Neyroud et al. · Circulation Cardiovascular Genetics · 2011 · 159 citations · Full text

Isoform-Specific Modulation of Voltage-Gated Na ⁺ Channels by Calmodulin

Isabelle Deschênes, Nathalie Neyroud, Deborah DiSilvestre et al. · Circulation Research · 2002 · 150 citations

Genomic Organization of the <i>KCNQ1</i> K ⁺ Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome

Nathalie Neyroud, Pascale Richard, Nicolas Vignier et al. · Circulation Research · 1999 · 113 citations