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Nature Communications|November 30, 2024
Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFRChristian M Boßelmann, Costin Leu, Tobias Brünger, et al.
International Journal of Medical Informatics|May 1, 2025
Ontology accelerates few-shot learning capability of large language model: A study in extraction of drug efficacy in a rare pediatric epilepsyPedram Golnari, Katrina Prantzalos, Veronica Hood, et al.
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Brain : a Journal of Neurology|October 15, 2019
Polygenic burden in focal and generalized epilepsiesCostin Leu, Remi Stevelink, Alexander W Smith, et al.
Epilepsy Research|July 30, 2015
Investigation of GRIN2A in common epilepsy phenotypesDennis Lal, Sandra Steinbrücker, Julian Schubert, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
Epilepsia|February 27, 2024
Genotype-phenotype associations in 1018 individuals with SCN1A-related epilepsiesDeclan Gallagher, Eduardo Pérez-Palma, Tobias Bruenger, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Long-Term Seizure Reduction Associated with Vagal Nerve Stimulation in Dravet SyndromeSunanjay Bajaj, Alina Ivaniuk, Tobias Bruenger, et al.
Iscience|January 7, 2021
Regulation of purine metabolism connects KCTD13 to a metabolic disorder with autistic featuresJon M Madison, Karen Duong, Ellen F Vieux, et al.
Brain Communications|November 26, 2020
Current knowledge of SLC6A1-related neurodevelopmental disordersKimberly Goodspeed, Eduardo Pérez-Palma, Sumaiya Iqbal, et al.
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