Kewalin Samart

ICePop links genetic risk to disease-relevant cellular states by analyzing single-cell transcriptomics data across multiple traits, identifying 1,684 disease-cell type associations.

This study identifies 64 FDA-approved drugs as potential host-directed therapeutics for tuberculosis using an integrative transcriptome-based approach combining multiple gene expression signatures and connectivity scoring methods.

The paper builds a mathematical model of the budding yeast START transition, integrating known molecular interactions and phenotypes to replicate key mutant behaviors and dynamics.