نتائج البحث - Elliott Rees
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Copy number variation and neuropsychiatric illness حسب Elliott Rees, George Kirov
منشور في 2021Revisão -
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Genetics of schizophrenia حسب Elliott Rees, Michael O’Donovan, Michael J. Owen
منشور في 2014Artigo -
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De Novo Mutation in Schizophrenia حسب Elliott Rees, George Kirov, Michael O’Donovan, Michael J. Owen
منشور في 2012Revisão -
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Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects حسب Kimberley Kendall, Elliott Rees, Valentina Escott‐Price, Mark Einon, Rhys H. Thomas, Jonathan Hewitt, Michael O’Donovan, Michael J. Owen, James Walters, George Kirov
منشور في 2016Artigo -
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Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank حسب Kimberley Kendall, Matthew Bracher‐Smith, H Fitzpatrick, Amy Lynham, Elliott Rees, Valentina Escott‐Price, Michael J. Owen, Michael O’Donovan, James Walters, George Kirov
منشور في 2019Artigo -
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Association of Rare Copy Number Variants With Risk of Depression حسب Kimberley Kendall, Elliott Rees, Matthew Bracher‐Smith, Sophie E. Legge, Lucy Riglin, Stanley Zammit, Michael O’Donovan, Michael John Owen, Ian Jones, George Kirov, James Walters
منشور في 2019Artigo -
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Genetic and Phenotypic Features of Schizophrenia in the UK Biobank حسب Sophie E. Legge, Antonio F. Pardiñas, Grace Woolway, Elliott Rees, Alastair G. Cardno, Valentina Escott‐Price, Peter Holmans, George Kirov, Michael J. Owen, Michael O’Donovan, James Walters
منشور في 2024Artigo -
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Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank حسب Karen Crawford, Matthew Bracher‐Smith, David Owen, Kimberley Kendall, Elliott Rees, Antonio F. Pardiñas, Mark Einon, Valentina Escott‐Price, James Walters, Michael O’Donovan, Michael J. Owen, George Kirov
منشور في 2018Artigo -
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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations حسب Elliott Rees, Hugo Creeth, Hai‐Gwo Hwu, Wei J. Chen, Ming T. Tsuang, Stephen J. Glatt, Romain Rey, George Kirov, James Walters, Peter Holmans, Michael J. Owen, Michael O’Donovan
منشور في 2021Artigo -
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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia حسب Andrew Pocklington, Elliott Rees, James Walters, Jun Han, David H. Kavanagh, Kimberly Chambert, Peter Holmans, Jennifer L. Moran, Steven A. McCarroll, George Kirov, Michael O’Donovan, Michael J. Owen
منشور في 2015Artigo -
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A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia حسب Lynsey S. Hall, Christopher W Medway, Oliver Pain, Antonio F. Pardiñas, Elliott Rees, Valentina Escott‐Price, Andrew Pocklington, Nicholas J. Bray, Peter Holmans, James Walters, Michael J. Owen, Michael O’Donovan
منشور في 2019Artigo -
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Common alleles contribute to schizophrenia in CNV carriers حسب Katherine E. Tansey, Elliott Rees, David E.J. Linden, Stephan Ripke, Kimberly D. Chambert, Jennifer L. Moran, Steven A. McCarroll, Peter Holmans, George Kirov, James Walters, Michael J. Owen, Michael O’Donovan
منشور في 2015Artigo -
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De novo CNVs in bipolar affective disorder and schizophrenia حسب Lyudmila Georgieva, Elliott Rees, Jennifer L. Moran, Kimberly D. Chambert, Vihra Milanova, Nicholas John Craddock, Shaun Purcell, Pamela Sklar, Steven A. McCarroll, Peter Holmans, Michael O’Donovan, Michael J. Owen, George Kirov
منشور في 2014Artigo -
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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia حسب Elliott Rees, Kimberley Kendall, Antonio F. Pardiñas, Sophie E. Legge, Andrew Pocklington, Valentina Escott‐Price, James H. MacCabe, David Collier, Peter Holmans, Michael O’Donovan, Michael J. Owen, James Walters, George Kirov
منشور في 2016Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Psychiatry
Schizophrenia (object-oriented programming)
Gene
Medicine
Genome
Copy-number variation
Psychology
Genotype
Phenotype
Single-nucleotide polymorphism
Cognition
Mutation
Neuroscience
Bipolar disorder
Autism
Environmental health
Population
Biobank
Exome sequencing
Allele
Internal medicine
Autism spectrum disorder
Disease
Exome
Gene duplication
Genome-wide association study
Intellectual disability
Neurodevelopmental disorder