Mélanie Quilès
Inserm(FR)Institute for Neurosciences of Montpellier(FR)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Retinal Development and Disorders, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Nitric Oxide and Endothelin Effects
Most-Cited Works
- → The genome of the social amoeba Dictyostelium discoideum(2005)1,364 cited
- → ER-mitochondria cross-talk is regulated by the Ca 2+ sensor NCS1 and is impaired in Wolfram syndrome(2018)153 cited
- → Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission(2017)121 cited
- → Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies(2015)73 cited
- → OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model(2018)72 cited
- → Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy(2019)65 cited
- → Increased steroidogenesis promotes early-onset and severe vision loss in females withOPA1dominant optic atrophy(2016)22 cited
- → ACO2 mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia(2018)20 cited
- → A dominant mutation inMAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium(2016)16 cited
- → Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy(2017)15 cited