ℹ️
🇬🇧
Search
Search for publications relevant for "genetics of epilepsy"
genetics of epilepsy
Publication
Class
Person
Publication
Programmes
publication
Genetics of epilepsy
2002 |
Publication without faculty affiliation
publication
The SCN1A gene analysis in patients with Febrile seizures
2006 |
Second Faculty of Medicine
publication
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations
2021 |
Second Faculty of Medicine
publication
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects
2020 |
Second Faculty of Medicine
publication
Childhood autism
2004 |
Second Faculty of Medicine
publication
Polygenic burden in focal and generalized epilepsies
2019 |
Second Faculty of Medicine
publication
The landscape of epilepsy-related GATOR1 variants
2019 |
Second Faculty of Medicine
publication
Familial temporal lobe epilepsy due to focal cortical dysplasia type IIIa
2015 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years
2023 |
Second Faculty of Medicine
publication
Novel approaches in pharmacological treatment of epilepsy
2021 |
Second Faculty of Medicine
publication
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
2019 |
Second Faculty of Medicine
publication
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
2021 |
Second Faculty of Medicine
publication
Trait impulsivity in Juvenile Myoclonic Epilepsy
2021 |
Second Faculty of Medicine
publication
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals
2021 |
Central Library of Charles University
publication
Genetic testing in children enrolled in epilepsy surgery program. A real-life study
2023 |
Second Faculty of Medicine, Central Library of Charles University
publication
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign genera lized epilepsy and beyond
2018 |
Second Faculty of Medicine