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Elliott Rees

Showing results (51-60 of 68) with videos related to

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Nature Communications|January 15, 2022
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variantsBret Sanders, Daniel D'Andrea, Mark O Collins, et al.
JAMA Psychiatry|September 26, 2019
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and TraitsSophie E Legge, Hannah J Jones, Kimberley M Kendall, et al.
Biological Psychiatry|November 14, 2018
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia PathogenesisElliott Rees, Noa Carrera, Joanne Morgan, et al.
Biological Psychiatry|March 8, 2021
Rare Copy Number Variants Are Associated With Poorer Cognition in SchizophreniaLeon Hubbard, Elliott Rees, Derek W Morris, 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.
Nature Neuroscience|January 15, 2020
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaElliott Rees, Jun Han, Joanne Morgan, et al.
BMC Medical Genetics|April 27, 2016
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyAndrew E Fry, Elliott Rees, Rose Thompson, et al.
Human Molecular Genetics|October 29, 2013
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Elliott Rees, James T R Walters, Kimberly D Chambert, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Nature Neuroscience|April 5, 2022
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onsetBranduff McAllister, Jasmine Donaldson, Caroline S Binda, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Nature Communications|January 15, 2022
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variantsBret Sanders, Daniel D'Andrea, Mark O Collins, et al.
JAMA Psychiatry|September 26, 2019
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and TraitsSophie E Legge, Hannah J Jones, Kimberley M Kendall, et al.
Biological Psychiatry|November 14, 2018
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia PathogenesisElliott Rees, Noa Carrera, Joanne Morgan, et al.
Biological Psychiatry|March 8, 2021
Rare Copy Number Variants Are Associated With Poorer Cognition in SchizophreniaLeon Hubbard, Elliott Rees, Derek W Morris, 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.
Nature Neuroscience|January 15, 2020
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaElliott Rees, Jun Han, Joanne Morgan, et al.
BMC Medical Genetics|April 27, 2016
Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyAndrew E Fry, Elliott Rees, Rose Thompson, et al.
Human Molecular Genetics|October 29, 2013
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Elliott Rees, James T R Walters, Kimberly D Chambert, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Nature Neuroscience|April 5, 2022
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onsetBranduff McAllister, Jasmine Donaldson, Caroline S Binda, et al.
Pageof 7