Singleton Ab 1

1. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
2. The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
3. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
4. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
1