Faghri F 1

1. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
2. 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)
3. The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
4. Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
5. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
6. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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