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Jennifer Crosbie

Showing results (121-130 of 136) with videos related to

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Biological Psychiatry|August 11, 2024
Brain-Charting Autism and Attention-Deficit/Hyperactivity Disorder Reveals Distinct and Overlapping NeurobiologySaashi A Bedford, Meng-Chuan Lai, Michael V Lombardo, et al.
Medrxiv : the Preprint Server for Health Sciences|December 18, 2023
Brain-charting autism and attention deficit hyperactivity disorder reveals distinct and overlapping neurobiologySaashi A Bedford, Meng-Chuan Lai, Michael V Lombardo, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2025
Genetics of Childhood-onset Systemic Lupus Erythematosus (cSLE)Raffaella Carlomagno, Nicholas Gold, Fangming Liao, et al.
The American Journal of Psychiatry|March 16, 2012
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3Nigel M Williams, Barbara Franke, Eric Mick, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, 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.
Molecular Autism|February 15, 2023
CRISIS AFAR: an international collaborative study of the impact of the COVID-19 pandemic on mental health and service access in youth with autism and neurodevelopmental conditionsBethany Vibert, Patricia Segura, Louise Gallagher, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, 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.
Pageof 14

Showing results (121-130 of 136) with videos related to

Sort By:
Pageof 14
Biological Psychiatry|August 11, 2024
Brain-Charting Autism and Attention-Deficit/Hyperactivity Disorder Reveals Distinct and Overlapping NeurobiologySaashi A Bedford, Meng-Chuan Lai, Michael V Lombardo, et al.
Medrxiv : the Preprint Server for Health Sciences|December 18, 2023
Brain-charting autism and attention deficit hyperactivity disorder reveals distinct and overlapping neurobiologySaashi A Bedford, Meng-Chuan Lai, Michael V Lombardo, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 13, 2025
Genetics of Childhood-onset Systemic Lupus Erythematosus (cSLE)Raffaella Carlomagno, Nicholas Gold, Fangming Liao, et al.
The American Journal of Psychiatry|March 16, 2012
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3Nigel M Williams, Barbara Franke, Eric Mick, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, 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.
Molecular Autism|February 15, 2023
CRISIS AFAR: an international collaborative study of the impact of the COVID-19 pandemic on mental health and service access in youth with autism and neurodevelopmental conditionsBethany Vibert, Patricia Segura, Louise Gallagher, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, 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.
Pageof 14