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

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent.

PloS one - 1 Jan 2015

Yang Hui, Wang Qian, Zheng Lei, Lin Min, Zheng Xiang-bin, Lin Fen, Yang Li-Ye

Abstract excerpt

The potential for genetic variation to modulate neonatal hyperbilirubinemia risk is increasingly being recognized. A case-control study was designed to assess comprehensive contributions of the multiple genetic modifiers of bilirubin metabolism on significant neonatal hyperbilirubinemia in Chinese descendents. Eleven common mutations and polymorphisms across five bilirubin metabolism genes, namely those encoding...

Read the complete abstract on PubMed

Topics

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

Share to Bilirubin
Share to Breast Feeding

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heme Oxygenase-1

Share to Hyperbilirubinemia, Neonatal

Share to Liver-Specific Organic Anion Transporter 1

Share to Organic Anion Transporters, Sodium-Independent

Share to Oxidoreductases Acting on CH-CH Group Donors

Share to Solute Carrier Organic Anion Transporter Family Member 1B3

Source

Open in PubMed Open full text

Identifiers

PMID: 26146841
DOI: 10.1371/journal.pone.0132034
PMCID: PMC4493094

Genes

BLVRA
HMOX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent.PMID 26146841Read ↗

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

Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population.Semantic proximity Read ↗

Associations between G6PD, OATP1B1 and BLVRA variants and susceptibility to neonatal hyperbilirubinaemia in a Chinese Han populationSemantic proximity Read ↗

Quantitative trait analysis of polymorphisms in two bilirubin metabolism enzymes to physiologic bilirubin levels in Chinese newborns.Semantic proximity Read ↗

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

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

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

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

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

Complex multifactorial nature of significant hyperbilirubinemia in neonates.Semantic proximity Read ↗

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