Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population

Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis

(2020) Jing Wang et al.   GENE

Uridine diphosphate glucuronosyltransferase 1A1

(2019) Glyn Steventon   XENOBIOTICA

UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children

(2018) Kuerbanjiang Abuduxikuer et al.   MEDICINE

Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II

(2017) Lei Sun et al.   MEDICINE

Genotype ofUGT1A1and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome

(2016) Yoshihiro Maruo et al.   JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Inherited disorders of bilirubin clearance

(2015) Naureen Memon et al.   PEDIATRIC RESEARCH

Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database

(2013) Giulia Canu et al.   BLOOD CELLS MOLECULES AND DISEASES

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

(2013) Lei-Lei Gu et al.   GENE

Eponym

(2011) Andrew Fretzayas et al.   EUROPEAN JOURNAL OF PEDIATRICS

Association of neonatal hyperbilirubinemia with uridine diphosphate-glucuronosyltransferase 1A1 gene polymorphisms: Meta-analysis

(2011) Jun Long et al.   PEDIATRICS INTERNATIONAL