Shashkin C 1

1. Validation of the Kazakh version of the movement disorder Society-Unified Parkinsons disease rating scale
2. BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients
3. A biobank for Parkinsons disease and atypical parkinsonism in central Asian and Transcaucasian regions
4. A glimpse of the genetics of young-onset Parkinson’s disease in Central Asia
5. Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia
6. Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency
7. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
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