A comprehensive analysis of SNCA -related genetic risk in sporadic parkinson disease-Reference-Cited by-同舟云学术

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A comprehensive analysis of SNCA -related genetic risk in sporadic parkinson disease

Published:2018-07 Issue:1 Volume:84 Page:117-129
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Pihlstrøm Lasse¹,Blauwendraat Cornelis²³,Cappelletti Chiara¹,Berge-Seidl Victoria¹,Langmyhr Margrete¹,Henriksen Sandra Pilar¹,van de Berg Wilma D. J.⁴,Gibbs J. Raphael³,Cookson Mark R.³,Singleton Andrew B.³,Nalls Mike A.³⁵,Toft Mathias¹⁶^ORCID, ,

Affiliation:

1. Department of Neurology; Oslo University Hospital; Oslo Norway

2. Neurodegenerative Diseases Research Unit; National Institute of Neurological Disorders and Stroke, National Institutes of Health; Bethesda MD

3. Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health; Bethesda MD

4. Department of Anatomy and Neurosciences, Clinical Neuroanatomy Section, Amsterdam Neuroscience; VU Medical Center; Amsterdam the Netherlands

5. Data Tecnica International; Glen Echo MD

6. Institute of Clinical Medicine; University of Oslo; Oslo Norway

Funder

Northern Ireland Chest, Heart and Stroke Association

Southern and Eastern Norway Regional Health Authority

Norges Forskningsråd

NIH

ZonMW Memorabel

Stichting Parkinson Fonds

Alzheimer Netherland-LECMA

F. Hoffmann-La Roche

Lysosomal Therapeutics

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.25274/fullpdf

Reference50 articles.

1. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease;Polymeropoulos;Science,1997

2. alpha-Synuclein locus triplication causes Parkinson's disease;Singleton;Science,2003

3. Genome-wide association study reveals genetic risk underlying Parkinson's disease;Simon-Sanchez;Nat Genet,2009

4. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease;Do;PLoS Genet,2011

5. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease;Nalls;Nat Genet,2014

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1. Regulatory miR-SNP rs4636297A > G in miR-126 is linked to increased risk of rigidity feature in patients with Parkinson’s disease;International Journal of Neuroscience;2024-09-02

2. Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing;npj Parkinson's Disease;2024-07-26

3. Epigenome-wide association study, meta-analysis and risk profiling of whole blood in Parkinson’s disease;2024-05-28

4. Parkinson’s Disease is Predominantly a Genetic Disease;Journal of Parkinson's Disease;2024-04-23

5. The Parkinson’s disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons;2024-03-19

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