James T. Pelekanos

The spectrum of SCN1A-related infantile epileptic encephalopathies

Louise A. Harkin, Jacinta M. McMahon, Xenia Iona et al. · Brain · 2007 · 527 citations · Full text

Scn1a Mutations, Subunit Gene Scn1a, Neurological Disorder +11

Mortality in Dravet syndrome

Monica S. Cooper, Anne M. McIntosh, Douglas E. Crompton et al. · Epilepsy Research · 2016 · 302 citations

Medicine, Dravet Syndrome, Degenerative Disease

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study

Samuel F. Berkovic, Louise A. Harkin, Jacinta M. McMahon et al. · The Lancet Neurology · 2006 · 293 citations

Retrospective Study, De-novo Mutations, Alleged Vaccine Encephalopathy +5

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Sarah E. Heron, Bronwyn E. Grinton, Sara Kivity et al. · The American Journal of Human Genetics · 2012 · 258 citations · Full text

Developmental Anomaly, Genetic Disorder, Choreoathetosis Syndrome +6

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

Bronwyn E. Grinton, Sarah E. Heron, James T. Pelekanos et al. · Epilepsia · 2015 · 125 citations