Annabelle Chaussenot

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot et al. · Brain · 2014 · 490 citations · Full text

Motor Neuron Disease, Genetics, Mitochondrial Myopathy +16

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

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

Sylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre et al. · Journal of Medical Genetics · 2013 · 189 citations · Full text

Neurologic features and genotype‐phenotype correlation in Wolfram syndrome

Annabelle Chaussenot, Sylvie Bannwarth, Cécile Rouzier et al. · Annals of Neurology · 2010 · 149 citations · Full text

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

Johann Böhm, Valérie Biancalana, Elizabeth T. DeChene et al. · Human Mutation · 2012 · 135 citations · Full text

Peripheral Neuropathy, Mendelian Disorder, Autoimmune Disease +15