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The Epilepsy Phenome/Genome Project (EPGP) informatics platform.
Nesbitt G, McKenna K, Mays V, Carpenter A, Miller K, Williams M; EPGP Investigators. Nesbitt G, et al. Int J Med Inform. 2013 Apr;82(4):248-59. doi: 10.1016/j.ijmedinf.2012.03.004. Epub 2012 May 10. Int J Med Inform. 2013. PMID: 22579394 Free PMC article.
The epilepsy phenome/genome project.
EPGP Collaborative; Abou-Khalil B, Alldredge B, Bautista J, Berkovic S, Bluvstein J, Boro A, Cascino G, Consalvo D, Cristofaro S, Crumrine P, Devinsky O, Dlugos D, Epstein M, Fahlstrom R, Fiol M, Fountain N, Fox K, French J, Freyer Karn C, Friedman D, Geller E, Glauser T, Glynn S, Haas K, Haut S, Hayward J, Helmers S, Joshi S, Kanner A, Kirsch H, Knowlton R, Kossoff E, Kuperman R, Kuzniecky R, Lowenstein D, McGuire S, Motika P, Nesbitt G, Novotny E, Ottman R, Paolicchi J, Parent J, Park K, Poduri A, Risch N, Sadleir L, Scheffer I, Shellhaas R, Sherr E, Shih JJ, Shinnar S, Singh R, Sirven J, Smith M, Sullivan J, Thio LL, Venkat A, Vining E, von Allmen G, Weisenberg J, Widdess-Walsh P, Winawer M. EPGP Collaborative, et al. Among authors: thio ll. Clin Trials. 2013 Aug;10(4):568-86. doi: 10.1177/1740774513484392. Epub 2013 Jul 1. Clin Trials. 2013. PMID: 23818435 Free PMC article.
Status epilepticus: For what are we waiting?
Thio LL, Wainwright MS. Thio LL, et al. Neurology. 2015 Jun 9;84(23):2296-7. doi: 10.1212/WNL.0000000000001670. Epub 2015 May 6. Neurology. 2015. PMID: 25948730 No abstract available.
Gain-of-function HCN2 variants in genetic epilepsy.
Li M, Maljevic S, Phillips AM, Petrovski S, Hildebrand MS, Burgess R, Mount T, Zara F, Striano P, Schubert J, Thiele H, Nürnberg P, Wong M, Weisenberg JL, Thio LL, Lerche H, Scheffer IE, Berkovic SF, Petrou S, Reid CA. Li M, et al. Among authors: thio ll. Hum Mutat. 2018 Feb;39(2):202-209. doi: 10.1002/humu.23357. Epub 2017 Nov 13. Hum Mutat. 2018. PMID: 29064616
79 results