Murphy D 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. Impact of COVID-19 Pandemic on Cardiovascular Testing in Asia: The IAEA INCAPS-COVID Study
6. Congenital heart disease in the ESC EORP Registry of Pregnancy and Cardiac disease (ROPAC)
7. Pregnancy outcomes in women after arterial switch operation for transposition of the great arteries: Results from ropac (registry of pregnancy and cardiac disease) of the european society of cardiology eurobservational research programme
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