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

Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis.

Metabolomics : Official journal of the Metabolomic Society - 8 Jan 2021

Fadista João, Skotte Line, Courraud Julie, Geller Frank, Gørtz Sanne, Wohlfahrt Jan, Melbye Mads, Cohen Arieh S, Feenstra Bjarke

Abstract excerpt

INTRODUCTION: Infantile hypertrophic pyloric stenosis (IHPS) is caused by hypertrophy of the pyloric sphincter muscle. OBJECTIVES: Since previous reports have implicated lipid metabolism, we aimed to (1) investigate associations between IHPS and a wide array of lipid-related metabolites in newborns, and (2) address whether detected differences in metabolite levels were likely to be driven by genetic differences...

Read the complete abstract on PubMed

Topics

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

Share to Feeding Behavior
Share to Biomarkers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromatography, Liquid

Share to Computational Biology

Share to Denmark

Share to Mass Spectrometry

Share to Metabolome

Share to Metabolomics

Source

Open in PubMed Open full text

Identifiers

PMID: 33417075
DOI: 10.1007/s11306-020-01763-2
PMCID: PMC7794101

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis.PMID 33417075Read ↗

Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.Semantic proximity Read ↗

Infantile hypertrophic pyloric stenosis: epidemiology, genetics, and clinical update.Semantic proximity Read ↗

Infantile hypertrophic pyloric stenosis--genetics and syndromes.Semantic proximity Read ↗

Genome-wide meta-analysis identifiesBARX1andEML4-MTA3as new loci associated with infantile hypertrophic pyloric stenosisSemantic proximity Read ↗

New insights into the pathogenesis of infantile pyloric stenosis.Semantic proximity Read ↗

Sex Affects Human Premature Neonates’ Blood Metabolome According to Gestational Age, Parenteral Nutrition, and Caffeine TreatmentSemantic proximity Read ↗

Gestational age-dependent development of the neonatal metabolomeSemantic proximity Read ↗

Similarities between acylcarnitine profiles in large for gestational age newborns and obesitySemantic proximity Read ↗

Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.Semantic proximity Read ↗

The floppy infant: contribution of genetic and metabolic disordersSemantic proximity Read ↗

Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.Semantic proximity Read ↗

Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.Semantic proximity Read ↗

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