Amedeo Bianchi

Spectrum of<i>SCN1A</i>mutations in severe myoclonic epilepsy of infancy

Rima Nabbout, Elena Di Gennaro, Bernardo Dalla Bernardina et al. · Neurology · 2003 · 245 citations

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert et al. · Human Molecular Genetics · 2012 · 149 citations · Full text

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

Federico Zara, Nicola Specchio, Pasquale Striano et al. · Epilepsia · 2013 · 122 citations · Full text

PRRT2 Mutations are the major cause of benign familial infantile seizures

Julian Schubert, Roberta Paravidino, Felicitas Becker et al. · Human Mutation · 2012 · 104 citations

Progressive myoclonic epilepsies

Silvana Franceschetti, Roberto Michelucci, Laura Canafoglia et al. · Neurology · 2014 · 102 citations · Full text