Zhu, Xiaolin

One gene, many neuropsychiatric disorders: lessons from Mendelian diseases

Zhu, X., Need, A. C., Petrovski, S., & Goldstein, D. B. (2014) · Nature Neuroscience

Genetic Associations and EpidemiologyGenetics and Neurodevelopmental Disorders

Cited by 131

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

Petrovski, S., Küry, S., Myers, C. T., Anyane-Yeboa, K., Cogné, B., Bialer, M., Xia, F., Hemati, P., Riviello, J., Mehaffey, M., et al. (2016) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 114

Asiaticoside inhibits TGF-β1-induced mesothelial-mesenchymal transition and oxidative stress via the Nrf2/HO-1 signaling pathway in the human peritoneal mesothelial cell line HMrSV5

Zhao, J., Shi, J., Shan, Y., Yu, M., Zhu, X., Zhu, Y., Liu, L., & Sheng, M. (2020) · Cellular & Molecular Biology Letters

Dialysis and Renal Disease ManagementTGF-β signaling in diseases

Cited by 55

Relationship between healthy lifestyle behaviors and cardiovascular risk factors in Chinese patients with type 2 diabetes mellitus: a subanalysis of the CCMR-3B STUDY

on behalf of CCMR-3B STUDY Investigators, Huang, Y., Li, J., Zhu, X., Sun, J., Ji, L., Hu, D., Pan, C., Tan, W., Jiang, S., et al. (2017) · Acta Diabetologica

Diabetes, Cardiovascular Risks, and LipoproteinsCardiovascular Health and Risk Factors

Cited by 21