ATP10B and the risk for Parkinson’s disease-Reference-Cited by-同舟云学术

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ATP10B and the risk for Parkinson’s disease

Published:2020-06-15 Issue:3 Volume:140 Page:401-402
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Real Raquel,Moore Anni,Blauwendraat Cornelis,Morris Huw R.,Bandres-Ciga Sara,

Funder

National Institutes of Health

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00401-020-02172-4.pdf

Reference3 articles.

1. Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L et al (2019) Parkinson’s disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. Mov Disord 34:866–875

2. Martin S, Smolders S, Van den Haute C, Heeman B, van Veen S, Crosiers D et al (2020) Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export. Acta Neuropathol. https://doi.org/10.1007/s00401-020-02145-7

3. Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D et al (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson’s disease: a meta-analysis of genome-wide association studies. Lancet Neurol 18:1091–1102

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1. Role of ATP10B in Parkinson disease in a cohort from southern Spain;Parkinsonism & Related Disorders;2024-07

2. Flipping the script: Advances in understanding how and why P4-ATPases flip lipid across membranes;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2024-04

3. Large-scale rare variant burden testing in Parkinson's disease;Brain;2023-06-22

4. The Endo-lysosomal System in Parkinson’s Disease: Expanding the Horizon;Journal of Molecular Biology;2023-06

5. Recent advances in novel mutation genes of Parkinson's disease;Journal of Neurology;2023-05-24

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