Skip to Main Content

Paper Details

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery.
EBioMedicine
8
2022
GGE, PRS, Patients, common genetic variants, epilepsies, epilepsy, familial epilepsies, familial epilepsy, focal epilepsy, genetic generalised epilepsy, non-familial (sporadic) epilepsies, patients
Author NameAffiliation
Ingrid E SchefferEpilepsy Research Centre, University of Melbourne, Royal Children's Hospital, The University of Melbourne, Australia The Florey Institute and Murdoch Children's Research Institute
Lynette G SadleirUniversity of Otago
Erin L HeinzenEshelman School of Pharmacy, University of North Carolina at Chapel Hill, USA Institute for Genomic Medicine, Columbia University Irving Medical Center
Ingo HelbigChildren's Hospital of Philadelphia
Melanie Bahlothe Walter and Eliza Hall Institute of Medical Research, the University of Melbourne
  • 1 - 5

Datasets

Release 1.2