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Central European Group on Genetics of Movement Disorders

Publication at First Faculty of Medicine, Second Faculty of Medicine |
2023

Abstract

Over the last two decades, we have witnessed major developments in neurogenetic research, the aetiopathogenesis and possible treatment options. Although substantial progress has been made, the first genome-wide studies have explained relatively little of the heritability of most complex traits, leading to a theory that a more fine-scale analysis considering the characteristics of individual populations may hold the key to the missing heritability.