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Ebiomedicine|June 9, 2022
The role of common genetic variation in presumed monogenic epilepsiesCiarán Campbell, Costin Leu, Yen-Chen Anne Feng, et al.Brain : a Journal of Neurology|February 28, 2023
Multimodal mapping of regional brain vulnerability to focal cortical dysplasiaHyo M Lee, Seok-Jun Hong, Ravnoor Gill, et al.Expert Review of Neurotherapeutics|July 2, 2019
Microbiota-gut brain axis involvement in neuropsychiatric disordersLuigi Francesco Iannone, Alberto Preda, Hervé M Blottière, et al.Epilepsia Open|December 11, 2019
Genomic and clinical predictors of lacosamide response in refractory epilepsiesSinéad B Heavin, Mark McCormack, Stefan Wolking, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.Orphanet Journal of Rare Diseases|September 28, 2015
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patientsEleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, et al.Plos Genetics|May 7, 2016
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental DisordersAnthony R Isles, Andrés Ingason, Chelsea Lowther, et al.Journal of Medical Genetics|July 1, 2016
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsyIris M de Lange, Katherine L Helbig, Sarah Weckhuysen, et al.Journal of Medical Genetics|March 19, 2016
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsyCyril Mignot, Celina von Stülpnagel, Caroline Nava, et al.Pageof 5