Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.

PloS one - 1 Jan 2014

Zhou Youyou, Wang San-nan, Li Hong, Zha Weifeng, Wang Xuli, Liu Yuanyuan, Sun Jian, Peng Qianqian, Li Shilin, Chen Ying, Jin Li

Abstract excerpt

A retrospective case control study of breast-fed full-term infants was carried out to determine whether variants in Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) and Heme Oxygenase-1 (HMOX1) were associated with neonatal hyperbilirubinemia. Eight genetic variants of UGT1A1 and 3 genetic variants of HMOX1 were genotyped in 170 hyperbilirubinemic newborns and 779 controls. Five significant associations...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to Breast Feeding

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucuronosyltransferase

Share to Heme Oxygenase-1

Share to Hyperbilirubinemia, Neonatal

Share to Infant

Share to Infant, Newborn

Source

Open in PubMed Open full text

Identifiers

PMID: 25102181
DOI: 10.1371/journal.pone.0104251
PMCID: PMC4125195

Genes

HMOX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.PMID 25102181Read ↗

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent.Semantic proximity Read ↗

UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.Semantic proximity Read ↗

Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.Semantic proximity Read ↗

UGT1A1 Mutation Association with Increased Bilirubin Levels and Severity of Unconjugated Hyperbilirubinemia in ABO Incompatible Newborns of ChinaSemantic proximity Read ↗

Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.Semantic proximity Read ↗

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China.Semantic proximity Read ↗

Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control StudySemantic proximity Read ↗

UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.Semantic proximity Read ↗

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern ChinaSemantic proximity Read ↗

Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia.Semantic proximity Read ↗

Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.Semantic proximity Read ↗

Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.