Stefan Wolking
RWTH Aachen University(DE)
Publications by Year
Research Areas
Epilepsy research and treatment, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Pharmacological Effects and Toxicity Studies, EEG and Brain-Computer Interfaces
Most-Cited Works
- → Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals(2019)299 cited
- → Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature(2015)299 cited
- → Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study(2018)93 cited
- → Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies(2017)78 cited
- → Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals(2021)59 cited
- → Antagonism of the mammalian target of rapamycin selectively mediates metabolic effects of epidermal growth factor receptor inhibition and protects human malignant glioma cells from hypoxia-induced cell death(2009)53 cited
- → Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy(2019)48 cited
- → Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview(2023)44 cited
- → Early-onset familial hemiplegic migraine due to a novel SCN1A mutation(2016)43 cited
- → The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies(2015)42 cited