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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Brett Trost

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Rheumatology (Oxford, England)|April 23, 2020

Associations of clinical and inflammatory biomarker clusters with juvenile idiopathic arthritis categoriesElham Rezaei, Daniel Hogan, Brett Trost, et al.

Neurology|February 13, 2026

Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained EpilepsyJimmy N H Nguyen, Maria Lachgar-Ruiz, Edward J Higginbotham, et al.

The New England Journal of Medicine|April 11, 2019

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.

CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.

NPJ Genomic Medicine|October 12, 2019

A large data resource of genomic copy number variation across neurodevelopmental disordersMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.

Nature Genetics|March 30, 2024

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.

Nature|May 13, 2026

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.

Cell|November 11, 2022

Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.

Biorxiv : the Preprint Server for Biology|June 26, 2025

Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.

Medrxiv : the Preprint Server for Health Sciences|August 12, 2025

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effectsWorrawat Engchuan, Omar Shanta, Kuldeep Kumar, et al.

Pageof 9

Search research articles

Showing results (81-90 of 90) with videos related to

Sort By:

Pageof 9

You have reached the last page of results.This site can display upto 90 results.

Rheumatology (Oxford, England)|April 23, 2020

Associations of clinical and inflammatory biomarker clusters with juvenile idiopathic arthritis categoriesElham Rezaei, Daniel Hogan, Brett Trost, et al.

Neurology|February 13, 2026

Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained EpilepsyJimmy N H Nguyen, Maria Lachgar-Ruiz, Edward J Higginbotham, et al.

The New England Journal of Medicine|April 11, 2019

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>André B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.

CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|February 13, 2018

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participantsMiriam S Reuter, Susan Walker, Bhooma Thiruvahindrapuram, et al.

NPJ Genomic Medicine|October 12, 2019

A large data resource of genomic copy number variation across neurodevelopmental disordersMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.

Nature Genetics|March 30, 2024

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsyDarcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.

Nature|May 13, 2026

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.

Cell|November 11, 2022

Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.

Biorxiv : the Preprint Server for Biology|June 26, 2025

Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.

Medrxiv : the Preprint Server for Health Sciences|August 12, 2025

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effectsWorrawat Engchuan, Omar Shanta, Kuldeep Kumar, et al.

Pageof 9