Follow
Ken Myers
Ken Myers
McGill University/Montreal Children's Hospital
Verified email at mcgill.ca
Title
Cited by
Cited by
Year
Heart rate variability in epilepsy: a potential biomarker of sudden unexpected death in epilepsy risk
KA Myers, LE Bello‐Espinosa, JD Symonds, SM Zuberi, R Clegg, ...
Epilepsia 59 (7), 1372-1380, 2018
1262018
The genetic landscape of epilepsy of infancy with migrating focal seizures
R Burgess, S Wang, A McTague, KE Boysen, X Yang, Q Zeng, KA Myers, ...
Annals of neurology 86 (6), 821-831, 2019
1132019
Epilepsy genetics: current knowledge, applications, and future directions
KA Myers, DL Johnstone, DA Dyment
Clinical genetics 95 (1), 95-111, 2019
1122019
Osteoblast-like cells and fluid flow: cytoskeleton-dependent shear sensitivity
KA Myers, JB Rattner, NG Shrive, DA Hart
Biochemical and biophysical research communications 364 (2), 214-219, 2007
1072007
Heart rate variability measurement in epilepsy: how can we move from research to clinical practice?
KA Myers, S Sivathamboo, P Perucca
Epilepsia 59 (12), 2169-2178, 2018
882018
Hydrostatic pressure sensation in cells: integration into the tensegrity model
KA Myers, JB Rattner, NG Shrive, DA Hart
Biochemistry and cell biology 85 (5), 543-551, 2007
742007
Genetic literacy series: genetic epilepsy with febrile seizures plus
KA Myers, IE Scheffer, SF Berkovic, ILAE Genetics Commission
Epileptic Disorders 20 (4), 232-238, 2018
702018
Stiripentol efficacy and safety in Dravet syndrome: a 12‐year observational study
KA Myers, P Lightfoot, SG Patil, JH Cross, IE Scheffer
Developmental Medicine & Child Neurology 60 (6), 574-578, 2018
592018
KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases
F Borlot, A Abushama, N Morrison‐Levy, P Jain, K Puthenveettil Vinayan, ...
Epilepsia 61 (4), 679-692, 2020
542020
Whole‐exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation
S Venkateswaran, KA Myers, AC Smith, CL Beaulieu, ...
Epilepsia 55 (7), e75-e79, 2014
482014
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability
F Borlot, BI de Almeida, SL Combe, DM Andrade, FM Filloux, KA Myers
Epilepsia 60 (8), 1661-1669, 2019
472019
Optic neuropathy in the context of leukemia or lymphoma: diagnostic approach to a neuro-oncologic emergency
KA Myers, A Nikolic, K Romanchuk, E Weis, MA Brundler, L Lafay-Cousin, ...
Neuro-Oncology Practice 4 (1), 60-66, 2017
472017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome
KA Myers, R Burgess, Z Afawi, JA Damiano, SF Berkovic, MS Hildebrand, ...
Epilepsia 58 (2), e26-e30, 2017
452017
GRIN2A-related speech disorders and epilepsy
KA Myers, IE Scheffer
442016
Hydrostatic pressure stimulation of human mesenchymal stem cells seeded on collagen-based artificial extracellular matrices
R Hess, T Douglas, KA Myers, B Rentsch, C Rentsch, H Worch, NG Shrive, ...
432010
ADGRV1 is implicated in myoclonic epilepsy
KA Myers, S Nasioulas, A Boys, JM McMahon, H Slater, P Lockhart, ...
Epilepsia 59 (2), 381-388, 2018
362018
DEPDC5 as a potential therapeutic target for epilepsy
KA Myers, IE Scheffer
Expert opinion on therapeutic targets 21 (6), 591-600, 2017
362017
Fatal cerebral edema with status epilepticus in children with Dravet syndrome: report of 5 cases
KA Myers, JM McMahon, SA Mandelstam, MT Mackay, RM Kalnins, ...
Pediatrics 139 (4), 2017
332017
Systematic review of MRI findings in children with developmental delay or cognitive impairment
K Murias, A Moir, KA Myers, I Liu, XC Wei
Brain and Development 39 (8), 644-655, 2017
322017
TUBA1A mutation associated with eye abnormalities in addition to brain malformation
KA Myers, LE Bello-Espinosa, A Kherani, XC Wei, AM Innes
Pediatric neurology 53 (5), 442-444, 2015
282015
The system can't perform the operation now. Try again later.
Articles 1–20