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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
Lubbe, Steven J; Escott-Price, Valentina; Gibbs, J Raphael; Nalls, Mike A; Bras, Jose; Price, T Ryan; Nicolas, Aude; Jansen, Iris E; Mok, Kin Y; Pittman, Alan M; Tomkins, James E; Lewis, Patrick A; Noyce, Alastair J; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R; Levine, Adam P; Brice, Alexis; Gasser, Thomas; Hardy, John; Heutink, Peter; Wood, Nicholas W; Singleton, Andrew B; Williams, Nigel M; Morris, Huw R.
Afiliación
  • Lubbe SJ; Department of Clinical Neuroscience, Institute of Neurology, University College London, London, UK.
  • Escott-Price V; Department of Psychological Medicine and Neurology, Institute of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
  • Gibbs JR; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
  • Nalls MA; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
  • Bras J; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Price TR; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
  • Nicolas A; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA.
  • Jansen IE; Department of Clinical Genetics, VU University Medical Center (VUmc), Amsterdam, The Netherlands.
  • Mok KY; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Pittman AM; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Tomkins JE; Division of Life Science, Hong Kong University of Science and Technology, Hong Kong SAR, People's Republic of China.
  • Lewis PA; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Noyce AJ; School of Pharmacy, University of Reading, Whiteknights, Reading, UK.
  • Lesage S; Centre for Integrated Neuroscience and Neurodynamics, University of Reading, Whiteknights, Reading, UK.
  • Sharma M; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.
  • Schiff ER; School of Pharmacy, University of Reading, Whiteknights, Reading, UK.
  • Levine AP; Centre for Integrated Neuroscience and Neurodynamics, University of Reading, Whiteknights, Reading, UK.
  • Brice A; Reta Lila Weston Institute, University College London Institute of Neurology, Queen Square, London, UK.
  • Gasser T; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
  • Hardy J; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, Tübingen, Germany.
  • Heutink P; Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Germany.
  • Wood NW; Division of Medicine, University College London, London, UK and 15UCL Genetics Institute, Department of Genetics, Environment and Evolution, University College London, London, UK.
  • Singleton AB; Division of Medicine, University College London, London, UK and 15UCL Genetics Institute, Department of Genetics, Environment and Evolution, University College London, London, UK.
  • Williams NM; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.
  • Morris HR; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Hum Mol Genet ; 25(24): 5483-5489, 2016 12 15.
Article en En | MEDLINE | ID: mdl-27798102
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Predisposición Genética a la Enfermedad / Herencia Multifactorial / Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Predisposición Genética a la Enfermedad / Herencia Multifactorial / Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article