Xiaojun Ren

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

A. Breman, J. Lupski, Zhihong Wu, 2020, Kidney international.

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

J. Lupski, Zhihong Wu, Shuyang Zhang, 2018, Human molecular genetics.

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice

J. Lupski, Zhihong Wu, Y. Li, 2019, Journal of Medical Genetics.

Single-cell transcriptomic analysis highlights origin and pathological process of human endometrioid endometrial carcinoma

Jianqing Liang, Yi-qin Wang, Xiaojun Chen, 2022, Nature Communications.

Modeling hepatoblastoma development with human fetal liver organoids reveals YAP1 activation is sufficient for tumorigenesis

Xinhua Lin, Jianqing Liang, Yufeng Zhang, 2021, Protein & Cell.

A Missense Mutation c.1132G > A in Fumarate Hydratase (FH) Leads to Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Syndrome and Insights into Clinical Management in Uterine Leiomyomata

Chao Wang, Yue Shi, Yiqing Chen, 2023, Genes.