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Brett Trost

Showing results (51-60 of 90) with videos related to

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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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 5, 2024
Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control studyPolina Perlman Danieli, Ny Hoang, Thanuja Selvanayagam, et al.
Journal of Medical Genetics|September 14, 2019
Impact of DNA source on genetic variant detection from human whole-genome sequencing dataBrett Trost, Susan Walker, Syed A Haider, et al.
Genes, Brain, and Behavior|February 15, 2024
Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorderDita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
PLOS Digital Health|March 2, 2026
Autism data sharing: Benefits, challenges, and recommendationsAlexandra Lautarescu, Brett Trost, Azadeh Kushki, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 8, 2021
Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillationJulieta Lazarte, Zachary W Laksman, Jian Wang, et al.
Cancers|September 9, 2022
Activation of the Anaphase Promoting Complex Reverses Multiple Drug Resistant Cancer in a Canine Model of Multiple Drug Resistant LymphomaTerra G Arnason, Valerie MacDonald-Dickinson, Matthew Casey Gaunt, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Molecular Psychiatry|May 13, 2022
Genome-wide tandem repeat expansions contribute to schizophrenia riskBahareh A Mojarad, Worrawat Engchuan, Brett Trost, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Long-read proteogenomic atlas of human neuronal differentiation reveals isoform diversity informing neurodevelopmental risk mechanismsNuo Xu, Katherine M Rynard, Elizabeth Radley, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 5, 2024
Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control studyPolina Perlman Danieli, Ny Hoang, Thanuja Selvanayagam, et al.
Journal of Medical Genetics|September 14, 2019
Impact of DNA source on genetic variant detection from human whole-genome sequencing dataBrett Trost, Susan Walker, Syed A Haider, et al.
Genes, Brain, and Behavior|February 15, 2024
Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorderDita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
PLOS Digital Health|March 2, 2026
Autism data sharing: Benefits, challenges, and recommendationsAlexandra Lautarescu, Brett Trost, Azadeh Kushki, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 8, 2021
Enrichment of loss-of-function and copy number variants in ventricular cardiomyopathy genes in 'lone' atrial fibrillationJulieta Lazarte, Zachary W Laksman, Jian Wang, et al.
Cancers|September 9, 2022
Activation of the Anaphase Promoting Complex Reverses Multiple Drug Resistant Cancer in a Canine Model of Multiple Drug Resistant LymphomaTerra G Arnason, Valerie MacDonald-Dickinson, Matthew Casey Gaunt, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Molecular Psychiatry|May 13, 2022
Genome-wide tandem repeat expansions contribute to schizophrenia riskBahareh A Mojarad, Worrawat Engchuan, Brett Trost, et al.
Biorxiv : the Preprint Server for Biology|December 25, 2025
Long-read proteogenomic atlas of human neuronal differentiation reveals isoform diversity informing neurodevelopmental risk mechanismsNuo Xu, Katherine M Rynard, Elizabeth Radley, et al.
Pageof 9