Philip Holmgren

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

Clinical spectrum of early-onset epileptic encephalopathies associated with <i>STXBP1</i> mutations

Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren et al. · Neurology · 2010 · 168 citations

Life Sciences, Genetics, Neurology +17

Reduction of seizure frequency after epilepsy surgery in a patient with <scp><i>STXBP1</i></scp> encephalopathy and clinical description of six novel mutation carriers

Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx et al. · Epilepsia · 2013 · 71 citations

Medicine, Genetics, Epileptology +16

Improving Care And Research Electronic Data Trust Antwerp (iCAREdata): a research database of linked data on out-of-hours primary care

Annelies Colliers, Stefaan Bartholomeeusen, Roy Remmen et al. · BMC Research Notes · 2016 · 32 citations · Full text

Computing, Biomedical Informatics, Health Informatics +17

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations

Joke Muys, Bettina Blaumeiser, Yves Jacquemyn et al. · Prenatal Diagnosis · 2018 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16