Katrien Smets

<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

De novo<i>SCN1A</i>mutations are a major cause of severe myoclonic epilepsy of infancy

Lieve Claes, Berten Ceulemans, Dominique Audenaert et al. · Human Mutation · 2003 · 202 citations

Life Sciences, Genetics, Neurology +17

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

Christian Beetz, Rebecca Schüle, Tine Deconinck et al. · Brain · 2008 · 180 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Loss of <i>TBK1</i> is a frequent cause of frontotemporal dementia in a Belgian cohort

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee et al. · Neurology · 2015 · 173 citations · Full text

Life Sciences, Genetics, Neurology +17

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Elodie Martin, Rebecca Schüle, Katrien Smets et al. · The American Journal of Human Genetics · 2013 · 171 citations · Full text

Life Sciences, Genetics, Neurology +10