Ana Borges-Correia

Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations

Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane et al. · Epilepsia · 2011 · 131 citations · Full text

Medicine, Genetics, Neurology +17

Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus

Pierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia et al. · The American Journal of Human Genetics · 2013 · 69 citations · Full text

Medicine, Genetics, Neuroscience +17

Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway

Jean‐Christophe Roux, Diana Zala, Nicolas Panayotis et al. · Neurobiology of Disease · 2011 · 64 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +7

Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse

Nicolas Panayotis, M. Pratte, Ana Borges-Correia et al. · Neurobiology of Disease · 2010 · 51 citations · Full text

Medicine, Neurobiology, Neuroscience +16

A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome

Valérie Matagne, Yann Ehinger, Lydia Saidi et al. · Neurobiology of Disease · 2016 · 45 citations · Full text

Life Sciences, Genetics, Neuroscience +7