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Jennifer L Howe

Showing results (11-20 of 38) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum DisorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Stem Cell Reports|November 6, 2018
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human NeuronsEric Deneault, Sean H White, Deivid C Rodrigues, et al.
Stem Cell Reports|February 14, 2019
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human NeuronsEric Deneault, Sean H White, Deivid C Rodrigues, et al.
Human Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.
Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
Human Mutation|January 30, 2022
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiencyYoel Gofin, Tianyun Wang, Madelyn A Gillentine, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Genetic variants in <i>DDX53</i> contribute to Autism Spectrum Disorder associated with the Xp22.11 locusMarcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
Nature Communications|October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorderAda J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Nature Medicine|January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorderRyan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum DisorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Stem Cell Reports|November 6, 2018
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human NeuronsEric Deneault, Sean H White, Deivid C Rodrigues, et al.
Stem Cell Reports|February 14, 2019
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human NeuronsEric Deneault, Sean H White, Deivid C Rodrigues, et al.
Human Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.
Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
Human Mutation|January 30, 2022
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiencyYoel Gofin, Tianyun Wang, Madelyn A Gillentine, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Genetic variants in <i>DDX53</i> contribute to Autism Spectrum Disorder associated with the Xp22.11 locusMarcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
Nature Communications|October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorderAda J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Nature Medicine|January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorderRyan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
Pageof 4