BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20250513T041914EDT-9989VlzG4O@132.216.98.100 DTSTAMP:20250513T081914Z DESCRIPTION:The Centre of Excellence in Epilepsy at The Neuro (Montreal Neu rological Institute-Hospital) is proud to announce the new Epilepsy Lectur e Series. The series will include eight lectures per year covering hot top ics in basic and clinical epilepsy research. Topics will be presented by d istinguished leaders and rising stars in the field\, with the goal of brid ging basic and clinical perspectives. We are most pleased to welcome Dr. S amuel Berkovic as the series’ first speaker.\n\nTo register: eventbrite\n \nLink to livestreaming: https://vimeo.com/662630742 (Q&A function is not accessible here)\n\nSpeaker: Dr. Sam Berkovic\, AM\, MD\, FAA\, FRACP\, FR S\n Laureate Professor\, Dept of Medicine\, University of Melbourne\n Direct or\, Epilepsy Research Centre at Austin Health\, Australia\n\nTalk Abstrac t - Whilst epilepsy may be a consequence of an acquired insult including t rauma\, stroke\, and brain tumours\, the genetic component to epilepsies h as been greatly under-estimated. Considerable progress has recently occurr ed in the understanding of epilepsy genetics\, both at a clinical genetic level and in the basic science of epilepsies. The clinical evidence for ge netic components will be first briefly discussed including data from popul ation studies\, twin analyses and multiplex family studies. Initial molecu lar discoveries occurred via classical methods of linkage and gene identif ication. Recent large-scale hypothesis-free whole exome studies searching for rare variants and genome-wide association studies detecting common var iants have been very rewarding. These discoveries have now impacted on cli nical practice\, especially in severe childhood epilepsies but increasingl y so in adult patients. The “genetic background” of patients has long been posited as part of the reason that some patients have epilepsy\, or perha ps why some have more severe epilepsy. This has been unmeasurable but now\ , with the development of polygenic risk scores\, the “background” is now in the research foreground. The current and future impact of polygenic ris k scores will be explored.\n DTSTART:20220120T210000Z DTEND:20220120T220000Z SUMMARY:NEURO Epilepsy Lecture Series: Epilepsy Genetics – From Family Stud ies to Polygenic Risk Scores URL:/neuro/channels/event/neuro-epilepsy-lecture-serie s-epilepsy-genetics-family-studies-polygenic-risk-scores-335811 END:VEVENT END:VCALENDAR