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Mandy Johnstone

Showing results (11-20 of 23) with videos related to

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Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|September 11, 2018
Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK BiobankMiruna C Barbu, Yanni Zeng, Xueyi Shen, et al.
Psychiatric Genetics|March 7, 2012
Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorderBenjamin Simon Pickard, Maarten J A Van Den Bossche, Mary P Malloy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 12, 2013
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disabilityEske M Derks, Muhammad Ayub, Kimberly Chambert, et al.
Nature Genetics|June 27, 2017
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disabilityTarjinder Singh, James T R Walters, Mandy Johnstone, et al.
Molecular Psychiatry|November 8, 2018
Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imagingMandy Johnstone, Navneet A Vasistha, Miruna C Barbu, et al.
Molecular Psychiatry|September 5, 2019
Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunctionNavneet A Vasistha, Mandy Johnstone, Samantha K Barton, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 10, 2025
Equitable Collaboration Between LMIC and HIC Researchers, Part I: A Preliminary Framework for Capacity Building in Psychiatric Genetics ResearchBrenda Cabrera-Mendoza, Margit Burmeister, Marcella Rietschel, et al.
Translational Psychiatry|September 8, 2018
DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illnessElise L V Malavasi, Kyriakos D Economides, Ellen Grünewald, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|September 11, 2018
Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK BiobankMiruna C Barbu, Yanni Zeng, Xueyi Shen, et al.
Psychiatric Genetics|March 7, 2012
Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorderBenjamin Simon Pickard, Maarten J A Van Den Bossche, Mary P Malloy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 12, 2013
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disabilityEske M Derks, Muhammad Ayub, Kimberly Chambert, et al.
Nature Genetics|June 27, 2017
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disabilityTarjinder Singh, James T R Walters, Mandy Johnstone, et al.
Molecular Psychiatry|November 8, 2018
Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imagingMandy Johnstone, Navneet A Vasistha, Miruna C Barbu, et al.
Molecular Psychiatry|September 5, 2019
Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunctionNavneet A Vasistha, Mandy Johnstone, Samantha K Barton, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 10, 2025
Equitable Collaboration Between LMIC and HIC Researchers, Part I: A Preliminary Framework for Capacity Building in Psychiatric Genetics ResearchBrenda Cabrera-Mendoza, Margit Burmeister, Marcella Rietschel, et al.
Translational Psychiatry|September 8, 2018
DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illnessElise L V Malavasi, Kyriakos D Economides, Ellen Grünewald, et al.
Pageof 3