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Elliott Rees

Showing results (31-40 of 68) with videos related to

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JAMA Psychiatry|April 18, 2019
Association of Rare Copy Number Variants With Risk of DepressionKimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, et al.
Human Molecular Genetics|November 14, 2012
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskJade Chapman, Elliott Rees, Denise Harold, et al.
The British Journal of Psychiatry : the Journal of Mental Science|June 4, 2019
Clinical indicators of treatment-resistant psychosisSophie E Legge, Charlotte A Dennison, Antonio F Pardiñas, et al.
JAMA Psychiatry|March 27, 2024
Genetic and Phenotypic Features of Schizophrenia in the UK BiobankSophie E Legge, Antonio F Pardiñas, Grace Woolway, et al.
Translational Psychiatry|February 27, 2019
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structuresMark Drakesmith, Greg D Parker, Jacqueline Smith, et al.
Human Molecular Genetics|July 25, 2014
De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L Moran, et al.
Journal of Medical Genetics|October 22, 2018
Medical consequences of pathogenic CNVs in adults: analysis of the UK BiobankKaren Crawford, Matthew Bracher-Smith, David Owen, et al.
Neuron|June 8, 2015
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaAndrew J Pocklington, Elliott Rees, James T R Walters, et al.
Nature Communications|September 10, 2021
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutationsElliott Rees, Hugo D J Creeth, Hai-Gwo Hwu, et al.
Molecular Psychiatry|October 20, 2020
Genetic association of FMRP targets with psychiatric disordersNicholas E Clifton, Elliott Rees, Peter A Holmans, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
JAMA Psychiatry|April 18, 2019
Association of Rare Copy Number Variants With Risk of DepressionKimberley Marie Kendall, Elliott Rees, Matthew Bracher-Smith, et al.
Human Molecular Genetics|November 14, 2012
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease riskJade Chapman, Elliott Rees, Denise Harold, et al.
The British Journal of Psychiatry : the Journal of Mental Science|June 4, 2019
Clinical indicators of treatment-resistant psychosisSophie E Legge, Charlotte A Dennison, Antonio F Pardiñas, et al.
JAMA Psychiatry|March 27, 2024
Genetic and Phenotypic Features of Schizophrenia in the UK BiobankSophie E Legge, Antonio F Pardiñas, Grace Woolway, et al.
Translational Psychiatry|February 27, 2019
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structuresMark Drakesmith, Greg D Parker, Jacqueline Smith, et al.
Human Molecular Genetics|July 25, 2014
De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L Moran, et al.
Journal of Medical Genetics|October 22, 2018
Medical consequences of pathogenic CNVs in adults: analysis of the UK BiobankKaren Crawford, Matthew Bracher-Smith, David Owen, et al.
Neuron|June 8, 2015
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaAndrew J Pocklington, Elliott Rees, James T R Walters, et al.
Nature Communications|September 10, 2021
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutationsElliott Rees, Hugo D J Creeth, Hai-Gwo Hwu, et al.
Molecular Psychiatry|October 20, 2020
Genetic association of FMRP targets with psychiatric disordersNicholas E Clifton, Elliott Rees, Peter A Holmans, et al.
Pageof 7