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Edward Yang

Showing results (151-160 of 181) with videos related to

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Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|June 21, 2022
Limited utility of structural MRI to identify the epileptogenic zone in young children with tuberous sclerosisMaaike Nijman, Edward Yang, Camilo Jaimes, et al.
Plos One|January 6, 2026
Elevated mortality and upregulated SARS-CoV-2-associated pathways in innate and adaptive immune cells from individuals with Down syndromeDaniella Balduino Victorino, Jackeline Moraes Malheiros, Felipe Ten-Caten, et al.
Annals of Neurology|February 11, 2026
Diverse Genetic Etiologies of Unilateral PolymicrogyriaAbbe Lai, Jennifer E Neil, Shyam K Akula, et al.
JACC. Basic to Translational Science|May 8, 2019
Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in SwineAlexis R Cole, Dorothy A Perry, Ali Raza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2Abbe Lai, Aubrie Soucy, Christelle Moufawad El Achkar, et al.
Epilepsia|January 26, 2019
Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding regionMcKenna Kelly, Meredith Park, Ivana Mihalek, et al.
Neuron|February 26, 2020
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5Andrew Kodani, Connor Kenny, Abbe Lai, et al.
The International Journal of Cardiovascular Imaging|June 5, 2025
Disparities in diagnosis and outcomes in American patients with transthyretin cardiac amyloidosisJoyce L Ngouchet Nouhossi, Iva Minga, Teodora Szasz, et al.
Molecular Genetics and Metabolism Reports|June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndromeAlcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2025
Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programsSara Bizzotto, Maya Talukdar, Edward A Stronge, et al.
Pageof 19

Showing results (151-160 of 181) with videos related to

Sort By:
Pageof 19
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|June 21, 2022
Limited utility of structural MRI to identify the epileptogenic zone in young children with tuberous sclerosisMaaike Nijman, Edward Yang, Camilo Jaimes, et al.
Plos One|January 6, 2026
Elevated mortality and upregulated SARS-CoV-2-associated pathways in innate and adaptive immune cells from individuals with Down syndromeDaniella Balduino Victorino, Jackeline Moraes Malheiros, Felipe Ten-Caten, et al.
Annals of Neurology|February 11, 2026
Diverse Genetic Etiologies of Unilateral PolymicrogyriaAbbe Lai, Jennifer E Neil, Shyam K Akula, et al.
JACC. Basic to Translational Science|May 8, 2019
Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in SwineAlexis R Cole, Dorothy A Perry, Ali Raza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2Abbe Lai, Aubrie Soucy, Christelle Moufawad El Achkar, et al.
Epilepsia|January 26, 2019
Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding regionMcKenna Kelly, Meredith Park, Ivana Mihalek, et al.
Neuron|February 26, 2020
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5Andrew Kodani, Connor Kenny, Abbe Lai, et al.
The International Journal of Cardiovascular Imaging|June 5, 2025
Disparities in diagnosis and outcomes in American patients with transthyretin cardiac amyloidosisJoyce L Ngouchet Nouhossi, Iva Minga, Teodora Szasz, et al.
Molecular Genetics and Metabolism Reports|June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndromeAlcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2025
Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programsSara Bizzotto, Maya Talukdar, Edward A Stronge, et al.
Pageof 19