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

The extent to which genotype information may add to the prediction of disturbed perinatal adaptation: none, minor, or major?

Pediatric research - 1 Nov 2007

Treszl András, Kaposi Ambrus, Hajdú Júlia, Szabó Miklós, Tulassay Tivadar, Vásárhelyi Barna

Abstract excerpt

Studies have been performed to describe the significance of genetic polymorphisms in complications associated with disturbed perinatal adaptation. Due to the large number of interacting factors, the results of classic statistical methods are often inconsistent. The random forest technique (RFT) is a robust nonparametric statistical approach that overcomes this problem through the calculation of the importance of...

Read the complete abstract on PubMed

Topics

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

Share to Acute Kidney Injury
Share to Ductus Arteriosus, Patent

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gestational Age

Share to Heart Failure

Share to Infant, Newborn, Diseases

Share to Infant, Premature

Share to Infant, Very Low Birth Weight

Share to Respiratory Distress Syndrome, Newborn

Source

Identifiers

PMID: 17805198
DOI: 10.1203/PDR.0b013e318155a0e1

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

The extent to which genotype information may add to the prediction of disturbed perinatal adaptation: none, minor, or major?PMID 17805198Read ↗

Published genetic variants in retinopathy of prematurity: random forest analysis suggests a negligible contribution to risk and severity.Semantic proximity Read ↗

Genetic Contributions to the Development of Complications in Preterm Newborns.Semantic proximity Read ↗

The Contribution of Commonly Diagnosed Genetic Disorders to Small for Gestational Age Birth and Subsequent Morbidity and Mortality in Preterm InfantsSemantic proximity Read ↗

Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm, and Term Infants.Semantic proximity Read ↗

Genetic score associations with birthweight in preterm-born infants compared with term-born infants.Semantic proximity Read ↗

Angiotensin-converting enzyme DD genotype is preventive against circulatory failure in very-low-birthweight neonates.Semantic proximity Read ↗

Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants.Semantic proximity Read ↗

The Role of Heme Oxygenase-1 Promoter Polymorphisms in Perinatal Disease.Semantic proximity Read ↗

Interleukin-6 polymorphism and bronchopulmonary dysplasia risk in very low-birthweight infants.Semantic proximity Read ↗

Polymorphisms in the Renin-Angiotensin system and outcome of very-low-birthweight infants.Semantic proximity Read ↗

The genetic contribution towards preterm delivery.Semantic proximity Read ↗

Genetic polymorphisms of heme-oxygenase 1 (HO-1) may impact on acute kidney injury, bronchopulmonary dysplasia, and mortality in premature infants.Semantic proximity Read ↗

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