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Epilepsia|February 27, 2024
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA studyHuantao Wen, Bin Wan, Taha Gholipour, et al.
Epilepsia|June 3, 2022
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataSeymour M Lopez, Leon M Aksman, Neil P Oxtoby, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
Global Socioeconomic Context and Brain Ageing in Epilepsy: an ENIGMA-Epilepsy studyHeath R Pardoe, Orrin Devinsky, Jemima Robson Bbiomed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2024
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disordersElisa Cali, Tania Quirin, Clarissa Rocca, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
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