Hasil Pencarian - Michael C O'Donovan

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  1. 1
    Pilot study to establish a prospective neonatal cohort: Study of Preterm Infants and Neurodevelopmental Genes (SPRING)

    Pilot study to establish a prospective neonatal cohort: Study of Preterm Infants and Neurodevelopmental Genes (SPRING) oleh Hilary S Wong, Michael C O'Donovan, Anita Thapar, Lucinda Hopkins

    Diterbitkan 2020-04-01
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  2. 2
    No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci.

    No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci. oleh Valentina Escott-Price, George Kirov, Elliott Rees, Anthony R Isles, Michael J Owen, Michael C O'Donovan

    Diterbitkan 2015-01-01
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  3. 3
    Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia

    Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia oleh Claire E. Tume, Sophie L. Chick, Peter A. Holmans, Elliott Rees, Michael C. O’Donovan, Darren Cameron, Nicholas J. Bray

    Diterbitkan 2024-09-01
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  4. 4
    SORL1 variants and risk of late-onset Alzheimer’s disease

    SORL1 variants and risk of late-onset Alzheimer’s disease oleh Yonghong Li, Charles Rowland, Joseph Catanese, John Morris, Simon Lovestone, Michael C. O’Donovan, Alison Goate, Michael Owen, Julie Williams, Andrew Grupe

    Diterbitkan 2008-02-01
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  5. 5
    Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

    Effects of pathogenic CNVs on physical traits in participants of the UK Biobank oleh David Owen, Mathew Bracher-Smith, Kimberley M. Kendall, Elliott Rees, Mark Einon, Valentina Escott-Price, Michael J. Owen, Michael C. O’Donovan, George Kirov

    Diterbitkan 2018-12-01
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  6. 6
    Common risk alleles for schizophrenia within the major histocompatibility complex predict white matter microstructure

    Common risk alleles for schizophrenia within the major histocompatibility complex predict white matter microstructure oleh Xavier Caseras, Emily Simmonds, Antonio F. Pardiñas, Richard Anney, Sophie E. Legge, James T. R. Walters, Neil A. Harrison, Michael C. O’Donovan, Valentina Escott-Price

    Diterbitkan 2024-04-01
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  7. 7
    Clozapine Metabolism is Associated With Absolute Neutrophil Count in Individuals With Treatment-Resistant Schizophrenia

    Clozapine Metabolism is Associated With Absolute Neutrophil Count in Individuals With Treatment-Resistant Schizophrenia oleh Isabella R. Willcocks, Sophie E. Legge, Mariana Nalmpanti, Lucy Mazzeo, Adrian King, John Jansen, Marinka Helthuis, Michael J. Owen, Michael C. O’Donovan, James T. R. Walters, Antonio F. Pardiñas

    Diterbitkan 2021-04-01
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  8. 8
    Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count

    Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count oleh Siobhan K. Lock, Sophie E. Legge, Djenifer B. Kappel, Isabella R. Willcocks, Marinka Helthuis, John Jansen, James T. R. Walters, Michael J. Owen, Michael C. O’Donovan, Antonio F. Pardiñas

    Diterbitkan 2023-10-01
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  9. 9
    Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank.

    Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank. oleh Charlotte A Dennison, Sophie E Legge, Matthew Bracher-Smith, Georgina Menzies, Valentina Escott-Price, Daniel J Smith, Aiden R Doherty, Michael J Owen, Michael C O'Donovan, James T R Walters

    Diterbitkan 2021-01-01
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  10. 10
    Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

    Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations oleh Elliott Rees, Hugo D. J. Creeth, Hai-Gwo Hwu, Wei J. Chen, Ming Tsuang, Stephen J. Glatt, Romain Rey, George Kirov, James T. R. Walters, Peter Holmans, Michael J. Owen, Michael C. O’Donovan

    Diterbitkan 2021-09-01
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  11. 11
    Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study

    Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study oleh Kimberley M. Kendall, Ann John, Sze Chim Lee, Elliott Rees, Antonio F. Pardiñas, Marcos Del Pozo Banos, Michael J. Owen, Michael C. O'Donovan, George Kirov, Keith Lloyd, Ian Jones, Sophie E. Legge, James T. R. Walters

    Diterbitkan 2020-11-01
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  12. 12
    Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts

    Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts oleh Viola Oertel-Knöchel, Thomas M. Lancaster, Christian Knöchel, Michael Stäblein, Helena Storchak, Britta Reinke, Alina Jurcoane, Jonathan Kniep, David Prvulovic, Kiran Mantripragada, Katherine E. Tansey, Michael C. O’Donovan, Michael J. Owen, David E.J. Linden

    Diterbitkan 2015-01-01
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  13. 13
    Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders

    Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders oleh Heath E. O’Brien, Eilis Hannon, Matthew J. Hill, Carolina C. Toste, Matthew J. Robertson, Joanne E. Morgan, Gemma McLaughlin, Cathryn M. Lewis, Leonard C. Schalkwyk, Lynsey S. Hall, Antonio F. Pardiñas, Michael J. Owen, Michael C. O’Donovan, Jonathan Mill, Nicholas J. Bray

    Diterbitkan 2018-11-01
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  14. 14
    All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs.

    All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. oleh Andrew J Schork, Wesley K Thompson, Phillip Pham, Ali Torkamani, J Cooper Roddey, Patrick F Sullivan, John R Kelsoe, Michael C O'Donovan, Helena Furberg, Tobacco and Genetics Consortium, Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, Nicholas J Schork, Ole A Andreassen, Anders M Dale

    Diterbitkan 2013-04-01
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  15. 15
    Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

    Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk var... oleh Bret Sanders, Daniel D’Andrea, Mark O. Collins, Elliott Rees, Tom G. J. Steward, Ying Zhu, Gareth Chapman, Sophie E. Legge, Antonio F. Pardiñas, Adrian J. Harwood, William P. Gray, Michael C. O’Donovan, Michael J. Owen, Adam C. Errington, Derek J. Blake, Daniel J. Whitcomb, Andrew J. Pocklington, Eunju Shin

    Diterbitkan 2022-01-01
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  16. 16
    Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.

    Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. oleh Ole A Andreassen, Wesley K Thompson, Andrew J Schork, Stephan Ripke, Morten Mattingsdal, John R Kelsoe, Kenneth S Kendler, Michael C O'Donovan, Dan Rujescu, Thomas Werge, Pamela Sklar, Psychiatric Genomics Consortium (PGC), Bipolar Disorder and Schizophrenia Working Groups, J Cooper Roddey, Chi-Hua Chen, Linda McEvoy, Rahul S Desikan, Srdjan Djurovic, Anders M Dale

    Diterbitkan 2015-11-01
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  17. 17
    Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

    Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate. oleh Ole A Andreassen, Wesley K Thompson, Andrew J Schork, Stephan Ripke, Morten Mattingsdal, John R Kelsoe, Kenneth S Kendler, Michael C O'Donovan, Dan Rujescu, Thomas Werge, Pamela Sklar, Psychiatric Genomics Consortium (PGC), Bipolar Disorder and Schizophrenia Working Groups, J Cooper Roddey, Chi-Hua Chen, Linda McEvoy, Rahul S Desikan, Srdjan Djurovic, Anders M Dale

    Diterbitkan 2013-04-01
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  18. 18
    Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

    Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD oleh Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, Tourette International Collaborative Genetics (TIC Genetics), Vanessa H. Bal, Kate Langley, Joanna Martin, Pieter J. Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A. Heiman, Jay A. Tischfield, Thomas V. Fernandez, Michael J. Owen, Michael C. O’Donovan, Anita Thapar, Matthew W. State, A. Jeremy Willsey

    Diterbitkan 2023-12-01
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  19. 19
    HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry

    HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry oleh Bettina Konte, James T. R. Walters, Dan Rujescu, Sophie E. Legge, Antonio F. Pardiñas, Dan Cohen, Munir Pirmohamed, Jari Tiihonen, Annette M. Hartmann, Jan P. Bogers, Jan van der Weide, Karen van der Weide, Anu Putkonen, Eila Repo-Tiihonen, Tero Hallikainen, Ed Silva, Oddur Ingimarsson, Engilbert Sigurdsson, James L. Kennedy, Patrick F. Sullivan, Marcella Rietschel, Gerome Breen, Hreinn Stefansson, Kari Stefansson, David A. Collier, Michael C. O’Donovan, Ina Giegling

    Diterbitkan 2021-04-01
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  20. 20
    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.

    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. oleh Bjarte Håvik, Franziska A Degenhardt, Stefan Johansson, Carla P D Fernandes, Anke Hinney, André Scherag, Helle Lybæk, Srdjan Djurovic, Andrea Christoforou, Kari M Ersland, Sudheer Giddaluru, Michael C O'Donovan, Michael J Owen, Nick Craddock, Thomas W Mühleisen, Manuel Mattheisen, Benno G Schimmelmann, Tobias Renner, Andreas Warnke, Beate Herpertz-Dahlmann, Judith Sinzig, Özgür Albayrak, Marcella Rietschel, Markus M Nöthen, Clive R Bramham, Thomas Werge, Johannes Hebebrand, Jan Haavik, Ole A Andreassen, Sven Cichon, Vidar M Steen, Stéphanie Le Hellard

    Diterbitkan 2012-01-01
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