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Developmental Medicine and Child Neurology|April 1, 2020
Sodium channel epilepsies and neurodevelopmental disorders: from disease mechanisms to clinical applicationAndreas Brunklaus, Dennis LalNeuron|July 27, 2018
Genetics Sheds New Light on Congenital Hydrocephalus BiologyDennis Lal, Aarno PalotieBrain Pathology (Zurich, Switzerland)|July 1, 2021
Application of single cell genomics to focal epilepsies: A call to actionSattar Khoshkhoo, Dennis Lal, Christopher A WalshNeurobiology of Disease|June 21, 2023
Technological and computational approaches to detect somatic mosaicism in epilepsyChristian M Boßelmann, Costin Leu, Dennis LalEuropean Journal of Human Genetics : EJHG|October 17, 2022
The phenotypic spectrum associated with loss-of-function variants in monogenic epilepsy genes in the general populationVictoria Smuk, Javier A López-Rivera, Costin Leu, et al.Nucleic Acids Research|May 23, 2019
Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar databaseEduardo Pérez-Palma, Marie Gramm, Peter Nürnberg, et al.The Lancet. Neurology|October 23, 2021
Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumoursIngmar Blumcke, Silvia Budday, Annapurna Poduri, et al.Frontiers in Neurology|April 19, 2021
ATP1A3-Related Disorders: An Ever-Expanding Clinical SpectrumPhilippe A Salles, Ignacio F Mata, Tobias Brünger, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Identification and quantification of oligogenic loss-of-function disordersArthur Stefanski, Eduardo Pérez-Palma, Marko Mrdjen, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 12, 2020
Time to move beyond genetics towards biomedical data-driven translational genomic research in severe paediatric epilepsiesAndreas Brunklaus, Costin Leu, Marie Gramm, et al.Pageof 15