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Jennifer L Howe

Showing results (1-10 of 38) with videos related to

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NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.
Molecular Autism|November 21, 2017
Mutations in <i>RAB39B</i> in individuals with intellectual disability, autism spectrum disorder, and macrocephalyMarc Woodbury-Smith, Eric Deneault, Ryan K C Yuen, et al.
NPJ Genomic Medicine|November 29, 2025
UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literatureMiriam S Reuter, Nelson Bautista Salazar, Jennifer L Howe, et al.
Human Genomics|November 22, 2021
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cellsNasna Nassir, Asma Bankapur, Bisan Samara, et al.
Molecular Psychiatry|May 2, 2022
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in DrosophilaAngelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, et al.
BMC Medical Genomics|January 12, 2023
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neuronsMuhammad Faheem, Eric Deneault, Roumiana Alexandrova, et al.
Elife|February 13, 2019
<i>CNTN5</i><sup>-</sup><i></i>or <i>EHMT2</i><sup>-</sup><i></i>human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networksEric Deneault, Muhammad Faheem, Sean H White, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
American Journal of Human Genetics|December 20, 2024
Chromosome X-wide common variant association study in autism spectrum disorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.
Molecular Autism|November 21, 2017
Mutations in <i>RAB39B</i> in individuals with intellectual disability, autism spectrum disorder, and macrocephalyMarc Woodbury-Smith, Eric Deneault, Ryan K C Yuen, et al.
NPJ Genomic Medicine|November 29, 2025
UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literatureMiriam S Reuter, Nelson Bautista Salazar, Jennifer L Howe, et al.
Human Genomics|November 22, 2021
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cellsNasna Nassir, Asma Bankapur, Bisan Samara, et al.
Molecular Psychiatry|May 2, 2022
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in DrosophilaAngelina Palacios-Muñoz, Danielle de Paula Moreira, Valeria Silva, et al.
BMC Medical Genomics|January 12, 2023
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neuronsMuhammad Faheem, Eric Deneault, Roumiana Alexandrova, et al.
Elife|February 13, 2019
<i>CNTN5</i><sup>-</sup><i></i>or <i>EHMT2</i><sup>-</sup><i></i>human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networksEric Deneault, Muhammad Faheem, Sean H White, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 7, 2020
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigreesMarc Woodbury-Smith, Mehdi Zarrei, John Wei, et al.
American Journal of Human Genetics|December 20, 2024
Chromosome X-wide common variant association study in autism spectrum disorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Pageof 4