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Showing results 1 to 4 of 4

Issue Date	Title	Author(s)	Type
2021	Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population	정지향	Article
2007	Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (CMTX5)	최병옥	Article
2020	Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals	김형래	Article
2022	Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association with Alzheimer Disease-Related Phenotypes	정지향	Article

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