University Of Perugia 1

1. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
2. Gendered Self-Views Across 62 Countries: A Test of Competing Models
3. 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)
4. The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
5. Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset
6. International declaration of adherence to treatment 2023 («omsk declaration»): presentation for russian readers
7. Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
8. TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
9. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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