Resultats de la cerca - Andrew Singleton

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  1. 1
    Exome sequencing: a transformative technology

    Exome sequencing: a transformative technology per Andrew Singleton

    Publicat 2011
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  2. 2
    The genetics and neuropathology of Parkinson’s disease

    The genetics and neuropathology of Parkinson’s disease per Henry Houlden, Andrew Singleton

    Publicat 2012
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  3. 3
    Genomewide Association Studies and Human Disease

    Genomewide Association Studies and Human Disease per John Hardy, Andrew Singleton

    Publicat 2009
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  4. 4
    The Evolution of Genetics: Alzheimer’s and Parkinson’s Diseases

    The Evolution of Genetics: Alzheimer’s and Parkinson’s Diseases per Andrew Singleton, John Hardy

    Publicat 2016
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  5. 5
    Application of Genome-Wide Single Nucleotide Polymorphism Typing: Simple Association and Beyond

    Application of Genome-Wide Single Nucleotide Polymorphism Typing: Simple Association and Beyond per J. Raphael Gibbs, Andrew Singleton

    Publicat 2006
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  6. 6
    Genome-wide association studies in neurological disorders

    Genome-wide association studies in neurological disorders per Javier Simón‐Sánchez, Andrew Singleton

    Publicat 2008
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  7. 7
    Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance

    Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance per Dena Hernández, Xylena Reed, Andrew Singleton

    Publicat 2016
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  8. 8
    The genetics of <scp>P</scp>arkinson's disease: Progress and therapeutic implications

    The genetics of <scp>P</scp>arkinson's disease: Progress and therapeutic implications per Andrew Singleton, Matthew J. Farrer, Vincenzo Bonifati

    Publicat 2013
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  9. 9
    The genetic architecture of Parkinson's disease

    The genetic architecture of Parkinson's disease per Cornelis Blauwendraat, Mike A. Nalls, Andrew Singleton

    Publicat 2019
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  10. 10
    Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease

    Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease per José Brás, Andrew Singleton, Mark Cookson, John Hardy

    Publicat 2008
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  11. 11
    LRRK2: Cause, Risk, and Mechanism

    LRRK2: Cause, Risk, and Mechanism per Coro Paisán‐Ruíz, Patrick A. Lewis, Andrew Singleton

    Publicat 2013
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  12. 12
    Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

    Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations per Rita Guerreiro, José Brás, John Hardy, Andrew Singleton

    Publicat 2014
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  13. 13
    Towards a complete resolution of the genetic architecture of disease

    Towards a complete resolution of the genetic architecture of disease per Andrew Singleton, John Hardy, Bryan J. Traynor, Henry Houlden

    Publicat 2010
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  14. 14
    Parkinson's disease and α‐synuclein expression

    Parkinson's disease and α‐synuclein expression per Michael J. Devine, Katrina Gwinn, Andrew Singleton, John Hardy

    Publicat 2011
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  15. 15
    DYT16: the original cases: Figure 1

    DYT16: the original cases: Figure 1 per Sarah Camargos, Andrew J. Lees, Andrew Singleton, Francisco Cardoso

    Publicat 2012
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  16. 16
    A large study reveals no association between APOE and Parkinson's disease

    A large study reveals no association between APOE and Parkinson's disease per Monica Federoff, Belén Jimenez‐Rolando, Michael A. Nalls, Andrew Singleton

    Publicat 2012
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  17. 17
    No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization study

    No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization study per Susanna C. Larsson, Andrew Singleton, Mike A. Nalls, J. Brent Richards

    Publicat 2017
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  18. 18
    Genetic risk factors in Parkinson’s disease

    Genetic risk factors in Parkinson’s disease per Kimberley J. Billingsley, Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Andrew Singleton

    Publicat 2018
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  19. 19
    Genetics of Parkinson's disease: An introspection of its journey towards precision medicine

    Genetics of Parkinson's disease: An introspection of its journey towards precision medicine per Sara Bandrés‐Ciga, Mónica Díez-Fairén, Jonggeol Jeff Kim, Andrew Singleton

    Publicat 2020
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  20. 20
    <i>SPG11</i> mutations are common in familial cases of complicated hereditary spastic paraplegia

    <i>SPG11</i> mutations are common in familial cases of complicated hereditary spastic paraplegia per Coro Paisán‐Ruíz, Okan Doğu, Ayça Dilara Yılmaz, Henry Houlden, Andrew Singleton

    Publicat 2008
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