Kaishibayeva G 1

1. Validation of the Kazakh version of the movement disorder Society-Unified Parkinsons disease rating scale
2. A biobank for Parkinsons disease and atypical parkinsonism in central Asian and Transcaucasian regions
3. A glimpse of the genetics of young-onset Parkinson’s disease in Central Asia
4. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
5. 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)
6. The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
7. Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset
8. Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
9. PEROXIDATION OF SALIVA LIPIDS IN PATIENTS WITH POSTCOVID SYNDROME DURING HIRUDOTHERAPY
10. TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
11. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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