E Peeters
Publications by Year
Research Areas
Epilepsy research and treatment, Pharmacological Effects and Toxicity Studies, Sleep and Wakefulness Research, Sleep and related disorders, Metabolism and Genetic Disorders
Most-Cited Works
- → Localization of the gene for Cowden disease to chromosome 10q22–23(1996)669 cited
- → Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome(2012)349 cited
- → Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations(1999)345 cited
- → Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood(2010)253 cited
- → Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan(2012)209 cited
- → Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: A genotype-phenotype study(2011)170 cited
- → Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis(2018)138 cited
- → Mortality Risk in Children With Epilepsy: The Dutch Study of Epilepsy in Childhood(2001)135 cited
- → Prognostic factors after a first attack of inflammatory CNS demyelination in children(2008)134 cited
- → The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families(2016)118 cited