Publications

Bina et al. (2020) De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of medical genetics, 57, 461-465. PMID: 31924697.

Ma et al. (2023) The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. Human Molecular Genetics, 32, 984-997. PMID: 36255738.