publication venue for
- 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