Developing enrichment analyzing methods at sub-cell type level to generate novel insights on complex disease pathogenesis

A benchmark of rare cell type detection methods for single-cell RNA sequencing data

Potential biomarkers for ALS/FTD as a consequence of TDP-43 loss of function

Uncovering the contribution of rare genetic variants in orofacial clefts

A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders