Valérie Chanavat

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

Gilles Millat, Philippe Chevalier, Lioara Restier‐Miron et al. · Clinical Genetics · 2006 · 106 citations

Life Sciences, Genetics, Molecular Genetics +16

Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy

Alexandre Janin, Kim‐Huong Thi Nguyen, Gilbert Habib et al. · Clinical Genetics · 2017 · 50 citations

Life Sciences, Cardiology, Genetics +14

Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies

Gilles Millat, Valérie Chanavat, Robert Rousson · Clinica Chimica Acta · 2014 · 47 citations

Medicine, Genetics, Molecular Genetics +14

Homozygous <i><scp>PKP2</scp></i> deletion associated with neonatal left ventricle noncompaction

Francis Ramond, Alexandre Janin, Sylvie Di Filippo et al. · Clinical Genetics · 2016 · 39 citations

Life Sciences, Cardiology, Genetics +16

Evaluation of a New High-Throughput Next-Generation Sequencing Method Based on a Custom AmpliSeq™ Library and Ion Torrent PGM™ Sequencing for the Rapid Detection of Genetic Variations in Long QT Syndrome

Gilles Millat, Valérie Chanavat, Robert Rousson · Molecular Diagnosis & Therapy · 2014 · 33 citations

Life Sciences, Genetics, Molecular Genetics +16