Genetics of epilepsy: Epilepsy Research Foundation workshop report

Author:

Sisodiya Sanjay1,Cross J. Helen1,Blümcke Ingmar1,Chadwick David1,Craig John1,Crino Peter B.1,Debenham Paul1,Delanty Norman1,Elmslie Frances1,Gardiner Mark1,Golden Jeffrey1,Goldstein David1,Greenberg David A.1,Guerrini Renzo1,Hanna Michael1,Harris John1,Harrison Paul1,Johnson Michael R.1,Kirov George1,Kullman Dimitri M.1,Makoff Andrew1,Marini Carla1,Nabbout Rima1,Nashef Lina1,Noebels Jeffrey L.1,Ottman Ruth1,Pirmohamed Munir1,Pitkänen Asla1,Scheffer Ingrid1,Shorvon Simon1,Sills Graeme1,Wood Nicholas1,Zuberi Sameer1

Affiliation:

1. Epilepsy Research Foundation United Kingdom

Abstract

ABSTRACT The Sixth Epilepsy Research Foundation workshop, held in Oxford in March 2006, brought together basic scientists, geneticists, epidemiologists, statisticians, pharmacologists and clinicians to consider progress, issues and strategies for harnessing genetics to improve the understanding and treatment of the epilepsies. General principles were considered, including the fundamental importance of clear study design, adequate patient numbers, defined phenotypes, robust statistical data handling, and follow‐up of genetic discoveries. Topics where some progress had been made were considered including chromosomal abnormalities, neurodevelopment, hippocampal sclerosis, juvenile myoclonic epilepsy, focal cortical dysplasia and pharmacogenetics. The ethical aspects of epilepsy genetics were reviewed. Principles and limitations of collaboration were discussed. Presentations and their matched discussions are produced here. There was optimism that further genetic research in epilepsy was not only feasible, but might lead to improvements in the lives of people with epilepsy.

Funder

Stanley Medical Research Institute

Wellcome

Publisher

Wiley

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