Bree Hodgson

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens, Boukje de Vries, Simona Donatello et al. · Nature Genetics · 2013 · 364 citations · Full text

Life Sciences, Genetics, Neuroscience +14

Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy

Samuel F. Berkovic, Sarah E. Heron, Lucio Giordano et al. · Annals of Neurology · 2004 · 276 citations

Life Sciences, Genetics, Neurology +17

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 · 261 citations · Full text

Medicine, Neurology, Neuroscience +14

<i>GABRA1</i> and <i>STXBP1</i> : Novel genetic causes of Dravet syndrome

Gemma L. Carvill, Sarah Weckhuysen, Jacinta M. McMahon et al. · Neurology · 2014 · 260 citations

Life Sciences, Genetics, Molecular Genetics +17

Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis

Samuel F. Berkovic, Leanne M. Dibbens, Alicia Oshlack et al. · The American Journal of Human Genetics · 2008 · 259 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12