Anja C. M. Sonsma

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek et al. · Nature Communications · 2018 · 493 citations · Full text

Epilepsy Therapies, Genetics, Genetic Epidemiology +22

Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in <i><scp>SCN</scp>1A</i>‐related seizure phenotypes

Iris Lange, Boudewijn Gunning, Anja C. M. Sonsma et al. · Epilepsia · 2018 · 155 citations · Full text

Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies

Dennis Lal, Ann‐Kathrin Ruppert, Holger Trucks et al. · PLoS Genetics · 2015 · 99 citations · Full text

Rare Microdeletions, Neurogenomics, Brain Development +31

Mosaicism of de novo pathogenic <i><scp>SCN</scp>1A</i> variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes

Iris Lange, Marco J. Koudijs, Ruben van ‘t Slot et al. · Epilepsia · 2018 · 64 citations · Full text

Outcomes and comorbidities of SCN1A-related seizure disorders

Iris Lange, Boudewijn Gunning, Anja C. M. Sonsma et al. · Epilepsy & Behavior · 2018 · 47 citations · Full text