Rik Hendrickx

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Arvid Suls, Johanna A. Jaehn, Angéla Kecskés et al. · The American Journal of Human Genetics · 2013 · 221 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Extending the <i>KCNQ2</i> encephalopathy spectrum

Sarah Weckhuysen, Vanja Ivanović, Rik Hendrickx et al. · Neurology · 2013 · 220 citations · Full text

Life Sciences, Genetics, Neurology +16

<i>GRIN2B</i> mutations in west syndrome and intellectual disability with focal epilepsy

Johannes R. Lemke, Rik Hendrickx, Kirsten Geider et al. · Annals of Neurology · 2013 · 211 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

Carolien G. F. de Kovel, Eva H. Brilstra, Marjan J. A. van Kempen et al. · Molecular Genetics & Genomic Medicine · 2016 · 91 citations · Full text

Life Sciences, Genetics, Neurology +15

Milky spots in the mouse omentum may play an important role in the origin of peritoneal macrophages

Josien F.A.M. Wijffels, Rik Hendrickx, Joke J. E. Steenbergen et al. · Research in Immunology · 1992 · 86 citations

Life Sciences, Cell Biology, Immunology +5