Audrey Mallet

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

Antoine Muchir, Jacques Médioni, M. Laluc et al. · Muscle & Nerve · 2004 · 170 citations

Life Sciences, Genetics, Molecular Biology +17

Penetrance of familial hypertrophic cardiomyopathy.

Philippe Charron, Lucie Carrier, Olivier Dubourg et al. · PubMed · 1997 · 92 citations

Life Sciences, Cardiology, Genetics +12

Rate dependence of sotalol-induced prolongation of ventricular repolarization during exercise in humans.

Christian Funck‐Brentano, Yves Kibleur, F. Le Coz et al. · Circulation · 1991 · 70 citations · Full text

Medicine, Cardiology, Pharmacology +17

Identification of the first nonsense<i>CDSN</i>mutation with expression of a truncated protein causing peeling skin syndrome type B

Audrey Mallet, Magdalini Kypriotou, Kelly M. George et al. · British Journal of Dermatology · 2013 · 31 citations

Medicine, Dermatology, Genetics +16

Dental and extra‐oral clinical features in 41 patients with <i><scp>WNT10A</scp></i> gene mutations: A multicentric genotype–phenotype study

C Tardieu, Sophie Jung, Karen Niederreither et al. · Clinical Genetics · 2017 · 31 citations

Life Sciences, Genetics, Oral Biology +15