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Paper Details

The role of common genetic variation in presumed monogenic epilepsies.
EBioMedicine
12
2022
DEEs, GGE, Human, ID, PRS, deleterious variant, developmental and epileptic encephalopathies, developmental delay, epilepsies, epilepsy, focal epilepsy, genetic generalised epilepsy, intellectual disability, monogenic epilepsies, monogenic severe epilepsy, monogenic, disorders, patients, people, person
Author NameAffiliation
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
Ingrid E SchefferUniversity of Melbourne, Austin and Royal Children's Hospitals, Australia Florey Institute and Murdoch Children's Research Institute
Sanjay M SisodiyaUCL Queen Square Institute of Neurology
Norman DelantyThe School of Pharmacy and Biomolecular Sciences, Beaumont Hospital
Gianpiero L CavalleriThe SFI FutureNeuro Research Centre, Republic of Ireland The School of Pharmacy and Biomolecular Sciences
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