Resultats de la cerca - Elliott Rees
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Copy number variation and neuropsychiatric illness per Elliott Rees, George Kirov
Publicat 2021Revisão -
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Genetics of schizophrenia per Elliott Rees, Michael O’Donovan, Michael J. Owen
Publicat 2014Artigo -
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De Novo Mutation in Schizophrenia per Elliott Rees, George Kirov, Michael O’Donovan, Michael J. Owen
Publicat 2012Revisão -
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Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects per Kimberley Kendall, Elliott Rees, Valentina Escott‐Price, Mark Einon, Rhys H. Thomas, Jonathan Hewitt, Michael O’Donovan, Michael J. Owen, James Walters, George Kirov
Publicat 2016Artigo -
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Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank per Kimberley Kendall, Matthew Bracher‐Smith, H Fitzpatrick, Amy Lynham, Elliott Rees, Valentina Escott‐Price, Michael J. Owen, Michael O’Donovan, James Walters, George Kirov
Publicat 2019Artigo -
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Association of Rare Copy Number Variants With Risk of Depression per 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
Publicat 2019Artigo -
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Genetic and Phenotypic Features of Schizophrenia in the UK Biobank per 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
Publicat 2024Artigo -
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Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank per 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
Publicat 2018Artigo -
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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations per 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
Publicat 2021Artigo -
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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia per 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
Publicat 2015Artigo -
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A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia per 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
Publicat 2019Artigo -
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Common alleles contribute to schizophrenia in CNV carriers per 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
Publicat 2015Artigo -
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De novo CNVs in bipolar affective disorder and schizophrenia per 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
Publicat 2014Artigo -
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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia per 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
Publicat 2016Artigo
Eines de cerca:
Matèries relacionades
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