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Nature|August 13, 2013
De novo mutations in epileptic encephalopathies, , Andrew S Allen, et al.
Epilepsia|January 10, 2018
Defining the phenotypic spectrum of SLC6A1 mutationsKatrine M Johannesen, Elena Gardella, Tarja Linnankivi, et al.
Brain : a Journal of Neurology|August 14, 2025
Associations between epilepsy-related polygenic risk and brain morphology in childhoodAlexander Ngo, Lang Liu, Sara Larivière, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With SCN2A-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2025
ASSOCIATIONS BETWEEN EPILEPSY-RELATED POLYGENIC RISK AND BRAIN MORPHOLOGY IN CHILDHOODAlexander Ngo, Lang Liu, Sara Larivière, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
The natural history of CDKL5 deficiency disorder into adulthoodAngel Aledo-Serrano, David Lewis-Smith, Helen Leonard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|January 20, 2026
Noise in the diagnosis of epilepsy by expertsFábio A Nascimento, John R McLaren, Wei Zhao, et al.
Neuroimage. Clinical|August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy studyEzequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances|November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA studySara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
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