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Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort.

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第一作者: Douglas P,Loesch
第一单位: Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA; Program in Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
作者单位: Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA; Program in Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA. [1] Department of Biostatistics, University of Washington, Seattle, WA, USA. [2] Lerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, OH, USA. [3] Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; Center for Global Health, Universidad Peruana Cayetano Heredia, Lima, Peru. [4] Movement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru. [5] Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru. [6] Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru. [7] Universidad Nacional del Altiplano, Puno, Peru. [8] Neurology Institute, Universidad de la República, Montevideo, Uruguay. [9] Department of Genetics, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. [10] Ribeirão Preto Medical School, Universidade de São Paulo, Ribeirão Preto, Brazil. [11] Movement Disorders Unit, Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil. [12] Departamento de Neurologia, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil. [13] Serviço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil; Departamento de Farmacologia, Universidade Federal do Rio Grande do Sul, Brazil. [14] Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil. [15] Neuroscience Research Group, Medical Research Institute, Faculty of Medicine, Universidad de Antioquia (UdeA), Medellín, Antioquia, Colombia. [16] CETRAM, Facultad de ciencias Medicas, Universidad de Santiago de Chile, Chile. [17] Neuroscience and Cell Death Research Groups, Medical School and Genetic Institute, Universidad Nacional de Colombia, Bogotá, Colombia. [18] Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, WA, USA. [19] Lerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, OH, USA; Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, WA, USA. Electronic address: matai@ccf.org. [20] Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, USA; Program in Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, MD, USA; Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA. Electronic address: timothydoconnor@gmail.com. [21]
DOI 10.1016/j.parkreldis.2022.06.010
PMID 35917738
发布时间 2024-09-23
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