Department Of Clinical And Movement Neurosciences 1

1. Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications
2. A glimpse of the genetics of young-onset Parkinson’s disease in Central Asia
3. Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment
4. Elucidating the genomic basis of rare pediatric neurological diseases in Central Asia and Transcaucasia
5. Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
6. The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
7. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
8. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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