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Joseph Buxbaum

Showing results (11-20 of 27) with videos related to

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Journal of the American Academy of Child and Adolescent Psychiatry|February 28, 2015
Randomized comparative trial of a social cognitive skills group for children with autism spectrum disorderLatha V Soorya, Paige M Siper, Todd Beck, et al.
Neurobiology of Aging|October 7, 2004
Abeta localization in abnormal endosomes: association with earliest Abeta elevations in AD and Down syndromeAnne M Cataldo, Suzana Petanceska, Nicole B Terio, et al.
European Journal of Human Genetics : EJHG|March 24, 2022
Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disabilityAlejandro J Brea-Fernández, Miriam Álvarez-Barona, Jorge Amigo, et al.
Molecular Autism|September 30, 2021
Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptomsM Pilar Trelles, Tess Levy, Bonnie Lerman, et al.
International Journal of Molecular Sciences|July 2, 2021
<i>KCNK18</i> Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel ActivityLisa Pavinato, Ehsan Nematian-Ardestani, Andrea Zonta, et al.
American Journal of Human Genetics|December 20, 2025
MIRAGE: A Bayesian statistical method for gene-level rare-variant analysis incorporating functional annotationsShengtong Han, Xiaotong Sun, Laura Sloofman, et al.
American Journal of Medical Genetics. Part A|March 6, 2021
Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature reviewLisa Pavinato, Slavica Trajkova, Enrico Grosso, et al.
Translational Psychiatry|July 10, 2022
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genesHiroki Kimura, Masahiro Nakatochi, Branko Aleksic, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or ArraysMatthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 25, 2008
A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithmsKatherine Gotham, Susan Risi, Geraldine Dawson, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

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Pageof 3
Journal of the American Academy of Child and Adolescent Psychiatry|February 28, 2015
Randomized comparative trial of a social cognitive skills group for children with autism spectrum disorderLatha V Soorya, Paige M Siper, Todd Beck, et al.
Neurobiology of Aging|October 7, 2004
Abeta localization in abnormal endosomes: association with earliest Abeta elevations in AD and Down syndromeAnne M Cataldo, Suzana Petanceska, Nicole B Terio, et al.
European Journal of Human Genetics : EJHG|March 24, 2022
Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disabilityAlejandro J Brea-Fernández, Miriam Álvarez-Barona, Jorge Amigo, et al.
Molecular Autism|September 30, 2021
Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptomsM Pilar Trelles, Tess Levy, Bonnie Lerman, et al.
International Journal of Molecular Sciences|July 2, 2021
<i>KCNK18</i> Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel ActivityLisa Pavinato, Ehsan Nematian-Ardestani, Andrea Zonta, et al.
American Journal of Human Genetics|December 20, 2025
MIRAGE: A Bayesian statistical method for gene-level rare-variant analysis incorporating functional annotationsShengtong Han, Xiaotong Sun, Laura Sloofman, et al.
American Journal of Medical Genetics. Part A|March 6, 2021
Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature reviewLisa Pavinato, Slavica Trajkova, Enrico Grosso, et al.
Translational Psychiatry|July 10, 2022
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genesHiroki Kimura, Masahiro Nakatochi, Branko Aleksic, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or ArraysMatthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 25, 2008
A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithmsKatherine Gotham, Susan Risi, Geraldine Dawson, et al.
Pageof 3