HuGE Literature Finder
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Loss-of-function variants in K 11.1 cardiac channels as a biomarker for SUDEP. Annals of clinical and translational neurology 2021 May . Soh Ming S, Bagnall Richard D, Bennett Mark F, Bleakley Lauren E, Mohamed Syazwan Erlina S, Marie Phillips A, Chiam Mathew D F, McKenzie Chaseley E, Hildebrand Michael, Crompton Douglas, Bahlo Melanie, Semsarian Christopher, Scheffer Ingrid E, Berkovic Samuel F, Reid Christopher |
Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing. Annals of human genetics 2019 Nov . Li Xin, Liu Nian, Bai Ro |
Genetic biomarkers for the risk of seizures in long QT syndrome. Neurology 2016 Oct 87 (16): 1660-1668. Auerbach David S, McNitt Scott, Gross Robert A, Zareba Wojciech, Dirksen Robert T, Moss Arthur |
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy. Annals of neurology 2015 Dec . Bagnall Richard D, Crompton Douglas E, Petrovski Slavé, Lam Lien, Cutmore Carina, Garry Sarah I, Sadleir Lynette G, Dibbens Leanne M, Cairns Anita, Kivity Sara, Afawi Zaid, Regan Brigid M, Duflou Johan, Berkovic Samuel F, Scheffer Ingrid E, Semsarian Christoph |
Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases. Brain pathology (Zurich, Switzerland) 2011 Mar 21 (2): 201-8. Tu Emily, Bagnall Richard D, Duflou Johan, Semsarian Christoph |
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