Florence Burté

CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

Emmanuelle C. Genin, Morgane Plutino, Sylvie Bannwarth et al. · EMBO Molecular Medicine · 2015 · 206 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous <i>OPA1</i> mutation

Ronen Spiegel, Ann Saada, Padraig J. Flannery et al. · Journal of Medical Genetics · 2015 · 115 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

metabolic profiling of Parkinson's disease and mild cognitive impairment

Florence Burté, David Houghton, Hannah Lowes et al. · Movement Disorders · 2017 · 81 citations · Full text

Life Sciences, Biochemistry, Neuroscience +17

Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy

Patrick Yu‐Wai‐Man, Devorah Soiferman, David Moore et al. · Mitochondrion · 2017 · 74 citations · Full text

Life Sciences, Cell Biology, Medicinal Chemistry +17

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

Cécile Rouzier, David Moore, Cécile Delorme et al. · Human Molecular Genetics · 2017 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17