We aim to uncover the genetic and epigenetic mechanisms underlying complex human diseases, and to translate those discoveries toward precision healthcare.
We aim to uncover the genetic and epigenetic mechanisms underlying complex human diseases. By integrating large-scale multi-omics datasets with advanced computational and systems-biology approaches, we seek to understand how genetic variants shape molecular regulation and contribute to disease risk.
Our research is grounded in basic medical science, but we aim to extend our findings toward medical applications and precision healthcare. By bridging genomics and medicine, we hope to identify novel biomarkers and therapeutic targets for human diseases.
We value an open and collaborative environment where curiosity, creativity, and persistence drive discovery. We welcome students and researchers who are eager to learn, explore, and contribute to a vibrant academic community.
