Elodie De Bruyckere

Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy

Sophie Nicole, Amina Chaouch, T. Torbergsen et al. · Brain · 2014 · 102 citations · Full text

Medicine, Genetics, Neurology +15

AP‐2 reduces amyloidogenesis by promoting BACE1 trafficking and degradation in neurons

Sujoy Bera, Santiago Camblor‐Perujo, Elena Calleja Barca et al. · EMBO Reports · 2020 · 62 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Autophagy regulates neuronal excitability by controlling cAMP/protein kinase A signaling at the synapse

Melina Overhoff, Frederik Tellkamp, Marianna Tolve et al. · The EMBO Journal · 2022 · 49 citations · Full text

Life Sciences, Neurobiology, Neuroscience +16

Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy

Stéphanie Bauché, Geoffroy Vellieux, Damien Sternberg et al. · Journal of Neurology · 2017 · 47 citations

Medicine, Genetics, Molecular Genetics +14

Structure‐function integrity of the adult hippocampus depends on the transcription factor <scp>Bcl11b</scp>/<scp>Ctip2</scp>

Ralph Simon, Lisa Baumann, Judith Fischer et al. · Genes Brain & Behavior · 2016 · 40 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17