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Epilepsy & Behavior : E&B|June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsyIngo Helbig, Corinna Hartmann, Heather C MeffordCurrent Opinion in Neurology|February 10, 2023
The current landscape of epilepsy genetics: where are we, and where are we going?Sarah M Ruggiero, Julie Xian, Ingo HelbigEuropean Journal of Human Genetics : EJHG|September 27, 2012
Familial cosegregation of rare genetic variants with disease in complex disordersIngo Helbig, Susan E Hodge, Ruth OttmanBioinformatics (Oxford, England)|July 8, 2010
CNVineta: a data mining tool for large case-control copy number variation datasetsMichael Wittig, Ingo Helbig, Stefan Schreiber, et al.Expert Review of Molecular Diagnostics|November 14, 2015
The contribution of next generation sequencing to epilepsy geneticsRikke S Møller, Hans A Dahl, Ingo HelbigEpilepsia|May 27, 2016
Primer Part 1-The building blocks of epilepsy geneticsIngo Helbig, Erin L Heinzen, Heather C Mefford, et al.Current Neurology and Neuroscience Reports|February 24, 2017
Epileptic Encephalopathies-Clinical Syndromes and Pathophysiological ConceptsMarkus von Deimling, Ingo Helbig, Eric D MarshEpilepsia|May 10, 2018
Genetic literacy series: Primer part 2-Paradigm shifts in epilepsy geneticsIngo Helbig, Erin L Heinzen, Heather C Mefford, et al.Advances in Neurobiology|July 5, 2017
Epileptic Encephalopathies as Neurodegenerative DisordersIngo Helbig, Markus von Deimling, Eric D MarshBiorxiv : the Preprint Server for Biology|February 24, 2025
Dual Translational Control in Cardiomyocytes by Heterogeneous mTORC1 and Hypertrophic ERK ActivationKeita Uchida, Emily A Scarborough, Benjamin L ProsserPageof 33