Juntendo University Faculty Of Medicine 1

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
4. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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