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Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
Annals of Clinical and Translational Neurology|May 18, 2021
Loss-of-function variants in Kv 11.1 cardiac channels as a biomarker for SUDEPMing S Soh, Richard D Bagnall, Mark F Bennett, et al.
Brain : a Journal of Neurology|April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsyChaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
The Journal of Clinical Investigation|November 25, 2025
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessiveKatrine M Johannesen, Khaing Phyu Aung, Vivian Wy Liao, et al.
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