Chen-Zhi Hao

Novel missense mutation in VPS33B is associated with isolated low gamma‐glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndrome

Jian-She Wang, Teng Liu, Jia-qi Li, 2019, Human mutation.

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations

C. Borchers, V. Ling, Jun Han, 2018, Liver international : official journal of the International Association for the Study of the Liver.

Defining pathogenicity of NOTCH2 variants for diagnosis of Alagille syndrome type 2 using a large cohort of patients

Yi Lu, Jian-She Wang, Li-Ting Li, 2022, Liver international : official journal of the International Association for the Study of the Liver.

Association of novel TMEM67 variants with mild phenotypes of high gamma‐glutamyl transpeptidase cholestasis and congenital hepatic fibrosis

Fengbin Wang, Jian-She Wang, M. Lian, 2022, Journal of cellular physiology.

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry

J. Zhao, K. Setchell, Yi Lu, 2017, Journal of pediatric gastroenterology and nutrition.

Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease

Tingting Li, Lian Chen, F. Lu, 2018, Scientific Reports.

Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis

Q. Xia, Yi Lu, Jian-She Wang, 2020, Journal of Medical Genetics.