Lieve Claes

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans et al. · The American Journal of Human Genetics · 2001 · 1.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls et al. · Annals of Neurology · 2011 · 514 citations

Medicine, Genetics, Neurology +17

Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1

Arvid Suls, Saul A. Mullen, Yvonne Weber et al. · Annals of Neurology · 2009 · 297 citations

Medicine, Genetics, Molecular Genetics +17

novoSNP, a novel computational tool for sequence variation discovery

Stefan Weckx, Jurgen Del‐Favero, Rosa Rademakers et al. · Genome Research · 2005 · 288 citations · Full text

Life Sciences, Bioinformatics, Genetics +17

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

Nanda A. Singh, Chris Pappas, E. Jill Dahle et al. · PLoS Genetics · 2009 · 265 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17