Laurence Richard

<i>INF2</i>Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

Olivia Boyer, Fabien Névo, Emmanuelle Plaisier et al. · New England Journal of Medicine · 2011 · 281 citations · Full text

Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

Estelle Colin, Evelyne Huynh Cong, Géraldine Mollet et al. · The American Journal of Human Genetics · 2014 · 132 citations · Full text

Galloway-mowat Syndrome, Disease Mechanism, Genetic Disorder +11

Microglia-neuron interaction at nodes of Ranvier depends on neuronal activity through potassium release and contributes to remyelination

Rémi Ronzano, Thomas Le Roux, Melina Thétiot et al. · Nature Communications · 2021 · 108 citations · Full text

TrkB-containing exosomes promote the transfer of glioblastoma aggressiveness to YKL-40-inactivated glioblastoma cells

Sandra Pinet, Barbara Bessette, Nicolas Védrenne et al. · Oncotarget · 2016 · 98 citations · Full text

Ykl-40-inactivated Glioblastoma Cells, Trkb-containing Exosomes, Extracellular Microvesicles +20

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

Julien Cassereau, Arnaud Chevrollier, Naïg Guéguen et al. · Neurogenetics · 2008 · 84 citations

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +8