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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
Discovery of drug-omics associations in type 2 diabetes with generative deep-learning models
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Further delineation of the KAT6B molecular and phenotypic spectrum
Persistent digestive disorders in the tropics: causative infectious pathogens and reference diagnostic tests