We aim to advance precision medicine using human genetics, multi-omics, stem cell models, and computational biology

We leverage large-scale genomic and multi-omic datasets to pinpoint the genetic drivers of human disease, fueling biomarker discovery and therapeutic innovation.

We integrate stem cell models and functional genomics to gain mechanistic insights and identify novel therapeutic targets, with a particular focus in neurological disease.

We develop machine learning and statistical genetics methods to improve our understanding of genetic variation in human populations and accelerate gene discovery.