Davide Mei

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

Russell J. Ferland, Luis Federico Bátiz, Jason Neal et al. · Human Molecular Genetics · 2008 · 182 citations · Full text

Idiopathic Epilepsies with Seizures Precipitated by Fever and <i>SCN1A</i> Abnormalities

Carla Marini, Davide Mei, Teresa Temudo et al. · Epilepsia · 2007 · 172 citations · Full text

<i>SCN1A</i> duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

Carla Marini, Ingrid E. Scheffer, Rima Nabbout et al. · Epilepsia · 2009 · 170 citations · Full text

Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes

Elena Parrini, Carla Marini, Davide Mei et al. · Human Mutation · 2016 · 162 citations