npj Parkinson's Disease Journal

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Overview

publication venue for

• Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson¿s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z).  12. 2026
• Insights into ancestral diversity in Parkinson¿s disease risk: a comparative assessment of polygenic risk scores.  11. 2025
• TMEM175, SCARB2 and CTSB associations with Parkinson¿s disease risk across populations.  11. 2025
• The LRRK2 p.L1795F variant causes Parkinson¿s disease in the European population.  11. 2025
• Author Correction: Elucidating causative gene variants in hereditary Parkinson¿s disease in the Global Parkinson¿s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9).  9. 2023
• Defining the causes of sporadic Parkinson¿s disease in the global Parkinson¿s genetics program (GP2).  9. 2023

Identity

International Standard Serial Number (ISSN)

• 23738057