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Brain : a Journal of Neurology
|
August 14, 2025
Associations between epilepsy-related polygenic risk and brain morphology in childhood
Alexander Ngo, Lang Liu, Sara Larivière, et al.
Neurology
|
July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related Disorders
Beatrice 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 CHILDHOOD
Alexander 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 adulthood
Angel 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 protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Neuroimage. Clinical
|
August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study
Ezequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances
|
November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
Sara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, 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 expression
Sara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA study
Huantao Wen, Bin Wan, Taha Gholipour, et al.
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Search research articles
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Showing results (651-660 of 674) with videos related to
Sort By:
Page
of 68
Brain : a Journal of Neurology
|
August 14, 2025
Associations between epilepsy-related polygenic risk and brain morphology in childhood
Alexander Ngo, Lang Liu, Sara Larivière, et al.
Neurology
|
July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related Disorders
Beatrice 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 CHILDHOOD
Alexander 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 adulthood
Angel 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 protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Neuroimage. Clinical
|
August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study
Ezequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances
|
November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
Sara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, 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 expression
Sara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Biorxiv : the Preprint Server for Biology
|
June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA study
Huantao Wen, Bin Wan, Taha Gholipour, et al.
Page
of 68