Wanshu Qi

The ability of an LC-MS/MS-based erythrocyte GALT enzyme assay to predict the phenotype in subjects with GALT deficiency.

S. Waisbren, G. Berry, H. Levy, 2019, Molecular genetics and metabolism.

Identification of TFPI as a receptor reveals recombination-driven receptor switching in Clostridioides difficile toxin B variants

Kuanwei Sheng, A. Doxey, D. Breault, 2022, Nature Communications.

5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy, and cerebral hypomyelination.

F. Eichler, J. Rabinowitz, G. Berry, 2018, Molecular genetics and metabolism.

Robust differentiation of human enteroendocrine cells from intestinal stem cells

J. Karp, Xiaolei Yin, Manasvi Shah, 2020, bioRxiv.

Arginine does not rescue p.Q188R mutation deleterious effect in classic galactosemia

W. Yue, L. V. van Loon, J. Bierau, 2018, Orphanet Journal of Rare Diseases.

Robust differentiation of human enteroendocrine cells from intestinal stem cells

J. Karp, Xiaolei Yin, Manasvi Shah, 2022, Nature Communications.

Emerging enterococcus pore-forming toxins with MHC/HLA-I as receptors

A. Earl, Kuanwei Sheng, M. Gilmore, 2022, Cell.

WNT2B Deficiency Causes Increased Susceptibility to Colitis in Mice and Impairs Intestinal Epithelial Development in Humans

Radhika S. Khetani, M. Helmrath, J. Thiagarajah, 2023, bioRxiv.