Arnaud Chevrollier

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot et al. · Brain · 2011 · 234 citations · Full text

Mitochondrial Myopathy, Genome Instability, Mfn2 Gene +14

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

Patrizia Amati‐Bonneau, Agnès Guichet, Aurélien Olichon et al. · Annals of Neurology · 2005 · 167 citations · Full text

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel <i>OPA1</i> mutations

Marc Ferré, Dominique Bonneau, Dan Miléa et al. · Human Mutation · 2009 · 162 citations · Full text

Mitochondrial coupling defect in Charcot–Marie–Tooth type 2A disease

Dominique Loiseau, Arnaud Chevrollier, Christophe Verny et al. · Annals of Neurology · 2007 · 155 citations

Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

Valérie Desquiret‐Dumas, Naïg Guéguen, Géraldine Leman et al. · Journal of Biological Chemistry · 2013 · 132 citations · Full text

Reductive Stress, Nadh Oxidation Responsible, Biochemistry +11