Associated Papers
Gene-environment interaction modifies the association between hyperinsulinemia and serum urate levels through SLC22A12.
Fujii W et al.
The Journal of Clinical Investigation, 2025
Characterization of a Compound Heterozygous SLC2A9 Mutation That Causes Hypouricemia.
Yoon J et al.
Biomedicines, 2021
Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals.
Cho SK et al.
Scientific Reports, 2020
Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels.
Misawa K et al.
Genetics, 2020
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels.
Tin A et al.
Nature Communications, 2018
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