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1. Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinsons Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)
2. Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
3. TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
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