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Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.Traffic (Copenhagen, Denmark)|April 29, 2006
Effects of dynactin disruption and dynein depletion on axonal microtubulesFridoon J Ahmad, Yan He, Kenneth A Myers, et al.Epilepsia|January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.American Journal of Medical Genetics. Part A|July 9, 2026
Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related DisorderDaniel Charouf, Andrea Accogli, Fadi F Hamdan, et al.Epilepsia|May 7, 2026
Management of ring chromosome 20 syndrome: Narrative review and consensus recommendationsAsma Khamis, Emilia Ricci, Maria Paola Canevini, et al.Pediatric Neurology|May 4, 2023
Awake Craniotomy Language Mapping in Children With Drug-Resistant Epilepsy due to Focal Cortical DysplasiaAriane St-Denis, Meredith Hooker, Katherine L'Abbée Lacas, et al.Cell Reports|June 15, 2017
Cytoplasmic Dynein Transports Axonal Microtubules in a Polarity-Sorting MannerAnand N Rao, Ankita Patil, Mark M Black, et al.Journal of Neurology|April 2, 2025
Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trialSaoussen Berrahmoune, Christelle Dassi, Heather Pekeles, et al.Epilepsia Open|June 6, 2023
Sleep and respiratory abnormalities in adults with developmental and epileptic encephalopathies using polysomnography and video-EEG monitoringShobi Sivathamboo, Kenneth A Myers, Andreas Pattichis, et al.American Journal of Medical Genetics. Part A|November 22, 2017
Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assayKenneth A Myers, Mark F Bennett, Chung W Chow, et al.Pageof 17