Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection studyHannah Spitzer, Anna Tietze, Mathilde Ripart et al.|Brain|2022Cited by 135
MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon GuidanceWilliam B. Dobyns, Grazia M.S. Mancini, Andrea Hanson‐Kahn et al.|The American Journal of Human Genetics|2018Cited by 85
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disordersJai Sidpra, Linda S. de Vries, Sniya Sudhakar et al.|Brain|2024Cited by 13
Automated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: <scp>AID</scp> ‐ <scp>HS</scp>Mathilde Ripart, Jordan DeKraker, Maria H. Eriksson et al.|Annals of Neurology|2024Cited by 11
Integrating standard epilepsy protocol, ASL-perfusion, MP2RAGE/EDGE and the MELD-FCD classifier in the detection of subtle epileptogenic lesions: a 3 Tesla MRI pilot studyLuigi Vincenzo Pastore, Felice D’Arco, Sniya Sudhakar et al.|Neuroradiology|2024Cited by 10