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Ellen Hanson

Showing results (21-30 of 43) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|October 3, 2025
The "Sensory Paradox": Exploring the Positive Association Between Hyper- and Hypo-Responsivity to Sensory Stimuli in Autism and BeyondKyle E Takach, Kacie Dunham-Carr, Gerardo Parra, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 30, 2020
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriersCaitlin M Hudac, Joanna Bove, Shelley Barber, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 29, 2017
Developmental trajectories for young children with 16p11.2 copy number variationRaphael Bernier, Caitlin M Hudac, Qixuan Chen, et al.
Clinical Genetics|July 30, 2025
Comprehensive Clinical Characteristics, Longitudinal Adaptive Functioning, and Electroencephalogram Activity in MAPK8IP3-Related Neurodevelopmental DisorderKhemika K Sudnawa, Alexa Geltzeiler, Cara H Kanner, et al.
The American Psychologist|April 5, 2019
Impacting development in infants with tuberous sclerosis complex: Multidisciplinary research collaborationMarian E Williams, Deborah A Pearson, Jamie K Capal, et al.
Epilepsia|November 7, 2019
Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational studyJoyce Y Wu, Monisha Goyal, Jurriaan M Peters, et al.
Molecular Genetics and Metabolism|February 7, 2025
The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolismItay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, et al.
Journal of Autism and Developmental Disorders|May 22, 2016
Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 DuplicationLeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, et al.
Expert Review of Neurotherapeutics|May 4, 2026
Rationale and study design for the first precision medicine randomized placebo-controlled trial in the 16p11.2 deletion syndromeHannah M Rea, Julia T Mattson, Vardan Arutiunian, et al.
JAMA Psychiatry|December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletionsAndres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Medrxiv : the Preprint Server for Health Sciences|October 3, 2025
The "Sensory Paradox": Exploring the Positive Association Between Hyper- and Hypo-Responsivity to Sensory Stimuli in Autism and BeyondKyle E Takach, Kacie Dunham-Carr, Gerardo Parra, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 30, 2020
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriersCaitlin M Hudac, Joanna Bove, Shelley Barber, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 29, 2017
Developmental trajectories for young children with 16p11.2 copy number variationRaphael Bernier, Caitlin M Hudac, Qixuan Chen, et al.
Clinical Genetics|July 30, 2025
Comprehensive Clinical Characteristics, Longitudinal Adaptive Functioning, and Electroencephalogram Activity in MAPK8IP3-Related Neurodevelopmental DisorderKhemika K Sudnawa, Alexa Geltzeiler, Cara H Kanner, et al.
The American Psychologist|April 5, 2019
Impacting development in infants with tuberous sclerosis complex: Multidisciplinary research collaborationMarian E Williams, Deborah A Pearson, Jamie K Capal, et al.
Epilepsia|November 7, 2019
Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational studyJoyce Y Wu, Monisha Goyal, Jurriaan M Peters, et al.
Molecular Genetics and Metabolism|February 7, 2025
The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolismItay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, et al.
Journal of Autism and Developmental Disorders|May 22, 2016
Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 DuplicationLeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, et al.
Expert Review of Neurotherapeutics|May 4, 2026
Rationale and study design for the first precision medicine randomized placebo-controlled trial in the 16p11.2 deletion syndromeHannah M Rea, Julia T Mattson, Vardan Arutiunian, et al.
JAMA Psychiatry|December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletionsAndres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Pageof 5