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Case Reports in Genetics|June 23, 2023
A Prenatal Presentation of CDK13-Related Disorder with a Novel Pathogenic VariantMichael Gibbs, Alysa Poulin, Yanwei Xi, et al.Accident; Analysis and Prevention|July 19, 2017
Detection of driver engagement in secondary tasks from observed naturalistic driving behaviorMengqiu Ye, Osama A Osman, Sherif Ishak, et al.Clinical Case Reports|July 20, 2023
New presentation of CLIFAHDD syndrome with a novel variant in NALCN gene: A report of a rare caseBita Hashemi, Richard J Huntsman, Huan Li, et al.Epilepsy & Behavior : E&B|January 17, 2025
"Clinical outcomes and healthcare costs in status epilepticus: A multivariable analysis from a tertiary center in a resource-limited setting"Mohsen Farjoud Kouhanjani, Mohammad Shafie'ei, Bita Hashemi, et al.Case Reports in Genetics|February 7, 2024
Constitutional Chromothripsis on Chromosome 2: A Rare Case with Severe PresentationAfia Hasnain, Laura L Thompson, Nicole L Hoppman, et al.Epilepsy & Behavior : E&B|September 16, 2023
Hypothalamic hamartoma surgery in a setting with limited resourcesAli A Asadi-Pooya, Mohamad S Masoudi, Bita Hashemi, et al.American Journal of Medical Genetics. Part A|May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric populationBita Hashemi, Anne Bassett, David Chitayat, et al.Journal of Neurodevelopmental Disorders|May 17, 2014
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problemsSébastien Chénier, Grace Yoon, Bob Argiropoulos, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 26, 2025
Mainstreaming of clinical genetic testing: A conceptual frameworkMichael P Mackley, Julie Richer, Andrea Guerin, et al.NPJ Genomic Medicine|June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric MedicineDimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.Pageof 1