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Louise Gallagher

Showing results (121-130 of 140) with videos related to

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The American Journal of Psychiatry|November 18, 2017
Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working GroupDaan van Rooij, Evdokia Anagnostou, Celso Arango, et al.
BMJ Open|June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registryMadeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
Nature Communications|November 2, 2019
Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasetsMerel C Postema, Daan van Rooij, Evdokia Anagnostou, 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.
Molecular Psychiatry|February 9, 2022
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortiumZhiqiang Sha, Daan van Rooij, Evdokia Anagnostou, 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.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Human Brain Mapping|May 19, 2020
Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventureMartine Hoogman, Daan van Rooij, Marieke Klein, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
The American Journal of Psychiatry|November 18, 2017
Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working GroupDaan van Rooij, Evdokia Anagnostou, Celso Arango, et al.
BMJ Open|June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registryMadeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
Nature Communications|November 2, 2019
Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasetsMerel C Postema, Daan van Rooij, Evdokia Anagnostou, 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.
Molecular Psychiatry|February 9, 2022
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortiumZhiqiang Sha, Daan van Rooij, Evdokia Anagnostou, 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.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Human Brain Mapping|May 19, 2020
Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventureMartine Hoogman, Daan van Rooij, Marieke Klein, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.
Pageof 14