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List of works by Xin-Hua Li

A novel ATP7B gene mutation in a liver failure patient with normal ceruloplasmin and low serum alkaline phosphatase

scientific article published on 27 October 2013

A novel homozygous no-stop mutation in G6PC gene from a Chinese patient with glycogen storage disease type Ia.

scientific article published on 16 December 2013

Association of Genetic Variation in Il28B with Hepatitis C Treatment-Induced Viral Clearance in the Chinese Han Population ⬇️

scientific article published on January 1, 2011

Association of Mutations in Toll-like Receptor 2 Signaling Genes With Fulminant Form of Hepatitis B-Related Acute Liver Failure.

scientific article

Association study of IFNAR2 and IL10RB genes with the susceptibility and interferon response in HBV infection

scientific article published on 01 September 2009

Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.

scientific article

Comparison of next-generation sequencing and clone-based sequencing in analysis of hepatitis B virus reverse transcriptase quasispecies heterogeneity.

scientific article published on 02 October 2013

Expression of MicroRNA-155 is Downregulated in Peripheral Blood Mononuclear Cells of Chronic Hepatitis B Patients.

scientific article published on 30 January 2016

IFI16 is involved in HBV-associated acute-on-chronic liver failure inflammation.

scientific article

Identification and validation of three core genes in p53 signaling pathway in hepatitis B virus-related hepatocellular carcinoma

scientific article published on 08 March 2021

Inherent lipid metabolic dysfunction in glycogen storage disease IIIa

scientific article published on 01 December 2014

N-glycosylation mutations within hepatitis B virus surface major hydrophilic region contribute mostly to immune escape.

scientific article published on 13 November 2013

Negative HBcAg in immunohistochemistry assay of liver biopsy is a predictive factor for the treatment of patients with nucleos(t)ide analogue therapy

scientific article

Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4.

scientific article

Recurrent porphyria attacks in a Chinese patient with a heterozygous PBGD mutation.

scientific article published on 29 April 2013

Soluble ST2 plasma concentrations predict mortality in HBV-related acute-on-chronic liver failure

scientific article

Unsupervised Clustering Reveals Distinct Subtypes of Biliary Atresia Based on Immune Cell Types and Gene Expression

scientific article published on 27 September 2021

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