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Editorial: Celebrating the Diversity of Genetic Research to Dissect the Pathogenesis of Parkinson's Disease.

作者信息

Farrer Matthew J, Bardien Soraya, Hattori Nobutaka, Lesage Suzanne, Ross Owen A, Mellick George D, Kruger Rejko

机构信息

Department of Neurology, University of Florida, Gainesville, FL, United States.

Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

出版信息

Front Neurol. 2021 Apr 6;12:648417. doi: 10.3389/fneur.2021.648417. eCollection 2021.

DOI:10.3389/fneur.2021.648417
PMID:33889126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8056125/
Abstract
摘要

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本文引用的文献

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.帕金森病的新风险基因座鉴定、因果关系洞察和遗传风险：全基因组关联研究的荟萃分析。
Lancet Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5.
2
Using global team science to identify genetic parkinson's disease worldwide.利用全球团队科学在全球范围内识别遗传性帕金森病。
Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26.
3
A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism.
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
在全球帕金森病遗传学项目（GP2）中确定散发性帕金森病的病因。
NPJ Parkinsons Dis. 2023 Sep 12;9(1):131. doi: 10.1038/s41531-023-00533-w.
4
Effect Modification between Genes and Environment and Parkinson's Disease Risk.基因与环境的交互作用与帕金森病风险。
Ann Neurol. 2022 Nov;92(5):715-724. doi: 10.1002/ana.26467. Epub 2022 Sep 24.
家族性帕金森病中α-突触核蛋白倍增的荟萃分析。
Front Neurol. 2018 Dec 11;9:1021. doi: 10.3389/fneur.2018.01021. eCollection 2018.
4
Global, regional, and national burden of Parkinson's disease, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.全球、地区和国家帕金森病负担，1990-2016 年：2016 年全球疾病负担研究的系统分析。
Lancet Neurol. 2018 Nov;17(11):939-953. doi: 10.1016/S1474-4422(18)30295-3. Epub 2018 Oct 1.
5
Global, regional, and national burden of neurological disorders during 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015.1990 - 2015年全球、区域和国家神经系统疾病负担：全球疾病负担研究2015的系统分析
Lancet Neurol. 2017 Nov;16(11):877-897. doi: 10.1016/S1474-4422(17)30299-5. Epub 2017 Sep 17.
6
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.神经芯片，NeuroX基因分型平台的升级版，用于快速筛查与神经系统疾病相关的变异。
Neurobiol Aging. 2017 Sep;57:247.e9-247.e13. doi: 10.1016/j.neurobiolaging.2017.05.009. Epub 2017 May 17.
7
Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.评估LRRK2与PARK16基因座之间的相互作用对帕金森病风险的影响：一项大型多中心研究分析
Neurobiol Aging. 2017 Jan;49:217.e1-217.e4. doi: 10.1016/j.neurobiolaging.2016.09.022. Epub 2016 Oct 6.
8
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease.帕金森病中多聚谷氨酰胺重复序列扩增的大规模评估。
Neurology. 2015 Oct 13;85(15):1283-92. doi: 10.1212/WNL.0000000000002016. Epub 2015 Sep 9.
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