Gabriel M. Ronen

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

Nanda A. Singh, Carole Charlier, Dora Stauffer et al. · Nature Genetics · 1998 · 1.2K citations

Channelopathies, Molecular Neuroscience, Hyperpolarization (Biology) +12

Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay

Darryl C. De Vivo, Rosario Rich Trifiletti, Ronald I. Jacobson et al. · New England Journal of Medicine · 1991 · 780 citations · Full text

Lipid Movement, Cellular Physiology, Cerebral Vascular Regulation +23

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler et al. · Nature Genetics · 2013 · 436 citations

Neurobiology Of Disease, Neurophysiology, Genetics +10

The epidemiology of clinical neonatal seizures in Newfoundland: A population-based study

Gabriel M. Ronen, Sharon Penney, Wayne L. Andrews · The Journal of Pediatrics · 1999 · 345 citations

Newborn Medicine, Clinical Neonatal Seizures, Pediatrics +1

Long-term prognosis in children with neonatal seizures

Gabriel M. Ronen, David Buckley, Sharon Penney et al. · Neurology · 2007 · 301 citations