• A large-scale whole-exome sequencing study involving 21,000 epilepsy patients and 33,000 controls has identified new genetic links to various epilepsy subtypes.
• The study highlights the significant role of genes encoding ion channels in multiple epilepsy subtypes, including epileptic encephalopathies and generalized and focal epilepsies.
• Researchers found subtype-specific genetic contributions, offering data-driven insights for understanding epilepsy biology and developing tailored diagnostic and treatment approaches.
• The Epi25 Collaborative's findings suggest potential therapeutic targets related to neuronal communication and synaptic transmission, with data accessible via an interactive browser.