Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

Oliver, K. L., Ellis, C. A., Scheffer, I. E., Ganesan, S., Leu, C., Sadleir, L. G., Heinzen, E. L., Mefford, H. C., Bass, A. J., Curtis, S. W., Harris, R. V., Whiteman, D. C., Helbig, I., Ottman, R., Epstein, M. P., Bahlo, M., & Berkovic, S. F. (2022). Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery. EBioMedicine, 81, 104079. https://doi.org/10.1016/j.ebiom.2022.104079
Authors:
Karen L. Oliver
Colin A. Ellis
Ingrid E. Scheffer
Shiva Ganesan
Costin Leu
Lynette G. Sadleir
Erin L. Heinzen
Heather C. Mefford
Andrew J. Bass
Sarah W. Curtis
Rebekah V. Harris
David C. Whiteman
Ingo Helbig
Ruth Ottman
Michael P. Epstein
Melanie Bahlo
Samuel F. Berkovic
Affiliated Authors:
Erin L. Heinzen
Ruth Ottman
Subjects:
Author Keywords:
common genetic variation
epilepsy genetics
familial epilepsies
polygenic risk scores
Publication Type:
Article
Unique ID:
10.1016/j.ebiom.2022.104079
PMID:
Journal:
Publication Date:
Data Source:
Scopus

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