Douglas E. Crompton

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens, Boukje de Vries, Simona Donatello et al. · Nature Genetics · 2013 · 358 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

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

Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy

Richard D. Bagnall, Douglas E. Crompton, Slavé Petrovski et al. · Annals of Neurology · 2015 · 274 citations

Mutations in mammalian target of rapamycin regulator <i>DEPDC5</i> cause focal epilepsy with brain malformations

Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan et al. · Annals of Neurology · 2014 · 218 citations · Full text

Genetics, Depdc5 Mutations, Disease Gene Identification +20

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation

Patrick F. Chinnery, Douglas E. Crompton, D. Birchall et al. · Brain · 2006 · 200 citations · Full text