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Tess Levy

Showing results (1-10 of 40) with videos related to

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Molecular Genetics & Genomic Medicine|February 22, 2022
Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxiaMary L Vo, Tess Levy, Shenela Lakhani, et al.
Journal of Child Neurology|October 18, 2023
Gait Abnormalities in Children with Phelan-McDermid SyndromeYitzchak Frank, Tess Levy, Reymundo Lozano, et al.
Frontiers in Psychiatry|March 11, 2025
Adolescents and adults with FOXP1 syndrome show high rates of anxiety and externalizing behaviors but not psychiatric decompensation or skill lossTess Levy, Hailey Silver, Renee Soufer, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 29, 2026
Prevalence of Phelan McDermid Syndrome Estimated To Be ~1:7300 Using a Multisource ModelTess Levy, David Lapidus, Kate Friedman, et al.
Human Genetics|July 16, 2023
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiencyTess Levy, Thariana Pichardo, Hailey Silver, et al.
Human Molecular Genetics|March 10, 2022
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptomsTess Levy, Bonnie Lerman, Danielle Halpern, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2025
Medicaid claims from 2008 to 2016 indicate low rates of genetic testing among children with intellectual disability and autism spectrum disorderTashalee R Brown, Wei-Lin Lee, Jonas Ventimiglia, et al.
Journal of Neurodevelopmental Disorders|April 2, 2026
Transient visual evoked potential abnormalities in ADNP syndromeTess Levy, Hailey Silver, Nurit Benrey, et al.
JAMA Network Open|September 19, 2025
Genetic Testing Among Medicaid-Insured Children With Autism and Intellectual DisabilityTashalee R Brown, Wei-Lin Lee, Jonas Ventimiglia, et al.
Genes|July 2, 2021
Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASDTeresa Tavassoli, Christina Layton, Tess Levy, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Molecular Genetics & Genomic Medicine|February 22, 2022
Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxiaMary L Vo, Tess Levy, Shenela Lakhani, et al.
Journal of Child Neurology|October 18, 2023
Gait Abnormalities in Children with Phelan-McDermid SyndromeYitzchak Frank, Tess Levy, Reymundo Lozano, et al.
Frontiers in Psychiatry|March 11, 2025
Adolescents and adults with FOXP1 syndrome show high rates of anxiety and externalizing behaviors but not psychiatric decompensation or skill lossTess Levy, Hailey Silver, Renee Soufer, et al.
Autism Research : Official Journal of the International Society for Autism Research|June 29, 2026
Prevalence of Phelan McDermid Syndrome Estimated To Be ~1:7300 Using a Multisource ModelTess Levy, David Lapidus, Kate Friedman, et al.
Human Genetics|July 16, 2023
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiencyTess Levy, Thariana Pichardo, Hailey Silver, et al.
Human Molecular Genetics|March 10, 2022
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptomsTess Levy, Bonnie Lerman, Danielle Halpern, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2025
Medicaid claims from 2008 to 2016 indicate low rates of genetic testing among children with intellectual disability and autism spectrum disorderTashalee R Brown, Wei-Lin Lee, Jonas Ventimiglia, et al.
Journal of Neurodevelopmental Disorders|April 2, 2026
Transient visual evoked potential abnormalities in ADNP syndromeTess Levy, Hailey Silver, Nurit Benrey, et al.
JAMA Network Open|September 19, 2025
Genetic Testing Among Medicaid-Insured Children With Autism and Intellectual DisabilityTashalee R Brown, Wei-Lin Lee, Jonas Ventimiglia, et al.
Genes|July 2, 2021
Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASDTeresa Tavassoli, Christina Layton, Tess Levy, et al.
Pageof 4