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Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.Epilepsia|May 18, 2021
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillationsRemi Stevelink, Jurjen J Luykx, Bochao D Lin, et al.Annals of Neurology|July 13, 2019
SSBP1 mutations in dominant optic atrophy with variable retinal degenerationNeringa Jurkute, Costin Leu, Hans-Martin Pogoda, et al.Biological Psychiatry Global Open Science|November 14, 2025
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 PatientsSlavina B Goleva, Costin Leu, Yen-Chen Anne Feng, et al.Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.Annals of Neurology|July 21, 2021
Postictal Psychosis in Epilepsy: A Clinicogenetic StudyVera Braatz, Helena Martins Custodio, Costin Leu, et al.Acta Neuropathologica|March 27, 2023
Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genesLucas Hoffmann, Roland Coras, Katja Kobow, et al.Acta Neuropathologica Communications|November 10, 2023
Deep histopathology genotype-phenotype analysis of focal cortical dysplasia type II differentiates between the GATOR1-altered autophagocytic subtype IIa and MTOR-altered migration deficient subtype IIbJonas Honke, Lucas Hoffmann, Roland Coras, et al.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.Brain : a Journal of Neurology|October 15, 2019
Polygenic burden in focal and generalized epilepsiesCostin Leu, Remi Stevelink, Alexander W Smith, et al.Pageof 7