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

Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms.

Pediatric research - 1 Sept 2022

Akat Ayberk, Yilmaz Semerci Seda, Ugurel Osman Mutluhan, Erdemir Aysegul, Danhaive Olivier, Cetinkaya Merih, Turgut-Balik Dilek

Abstract excerpt

AIM: Genetic variants contribute to the pathogenesis of bronchopulmonary dysplasia (BPD). The aim of this study is to evaluate the association of 45 SNPs with BPD susceptibility in a Turkish premature infant cohort. METHODS: Infants with gestational age <32 weeks were included. Patients were divided into BPD or no-BPD groups according to oxygen need at 28 days of life, and stratified according to the severity...

Read the complete abstract on PubMed

Topics

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

Share to Bronchopulmonary Dysplasia
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Infant, Premature

Share to Kruppel-Like Transcription Factors

Share to Mannose-Binding Lectin

Share to Oxygen

Share to Sulfotransferases

Share to Wnt Signaling Pathway

Source

Identifiers

PMID: 34853430
DOI: 10.1038/s41390-021-01851-6

Genes

CHST9
KLF12
WNT5A
CEP170
IMPACT
MAGI2
MBL2
NFKBIA
VEGFA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms.PMID 34853430Read ↗

Genetic and epidemiological risk factors in the development of bronchopulmonary dysplasia.Semantic proximity Read ↗

Genetic predisposing factors to bronchopulmonary dysplasia: preliminary data from a multicentre study.Semantic proximity Read ↗

Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical InformationSemantic proximity Read ↗

Genetic predisposition to bronchopulmonary dysplasia.Semantic proximity Read ↗

Role of Single Nucleotide Fibronectin Polymorphisms in Pathogenesis of Bronchopulmonary DysplasiaSemantic proximity Read ↗

Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.Semantic proximity Read ↗

The genetic predisposition to bronchopulmonary dysplasia.Semantic proximity Read ↗

Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.Semantic proximity Read ↗

Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.Semantic proximity Read ↗

Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role.Semantic proximity Read ↗

Integrated genomic analyses in bronchopulmonary dysplasia.Semantic proximity Read ↗

Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia.Semantic proximity Read ↗

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