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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.
American Journal of Medical Genetics. Part A|October 8, 2020
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrumYanick J Crow, Heather Marshall, Gillian I Rice, et al.
Human Brain Mapping|May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data setsSanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Nature Communications|July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expressionSara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Brain : a Journal of Neurology|August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy studySean N Hatton, Khoa H Huynh, Leonardo Bonilha, et al.
Neurology|August 22, 2025
Changes in Gray Matter Morphology and White Matter Microstructure Across the Adult Lifespan in People With Temporal Lobe EpilepsyJudy Chen, Alexander Ngo, Raul Rodriguez-Cruces, et al.
Brain : a Journal of Neurology|March 25, 2022
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsyBo-Yong Park, Sara Larivière, Raul Rodríguez-Cruces, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
A WORLDWIDE ENIGMA STUDY ON EPILEPSY-RELATED GRAY AND WHITE MATTER COMPROMISE ACROSS THE ADULT LIFESPANJudy Chen, Alexander Ngo, Raúl Rodríguez-Cruces, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiencyAsh Zawerton, Cyril Mignot, Ashley Sigafoos, et al.
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