Leanne M. Dibbens

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

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

Leanne M. Dibbens, Patrick Tarpey, Kim Hynes et al. · Nature Genetics · 2008 · 441 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +11

Truncation of the GABAA-Receptor γ2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures Plus

Louise A. Harkin, David N. Bowser, Leanne M. Dibbens et al. · The American Journal of Human Genetics · 2002 · 439 citations · Full text

Generalized Epilepsy, Neurobiology Of Disease, Neurophysiology +9

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

Sarah E. Heron, Katherine R. Smith, Melanie Bahlo et al. · Nature Genetics · 2012 · 405 citations · Full text

Channelopathies, Missense Mutations, Hyperpolarization (Biology) +11

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