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

Hypertriglyceridemia: phenomics and genomics.

Molecular and cellular biochemistry - 1 Jun 2009

Hegele Robert A, Pollex Rebecca L

Abstract excerpt

Hypertriglyceridemia is a common complex metabolic trait that is associated with increased atherosclerosis risk, presence of the metabolic syndrome and, with extreme elevation, increased risk of pancreatitis. Hierarchical cluster analysis using clinical and biochemical features of the Frederickson hyperlipoproteinemia types can generate hypotheses for molecular genetic studies. High throughput resequencing of...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Atherosclerosis
Share to Cluster Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Genomics

Share to Genotype

Share to Hypertriglyceridemia

Share to Pancreatitis

Source

Identifiers

PMID: 19130180
DOI: 10.1007/s11010-008-0005-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hypertriglyceridemia: phenomics and genomics.PMID 19130180Read ↗

Understanding Hypertriglyceridemia: Integrating Genetic InsightsSemantic proximity Read ↗

The Genetic Basis of Hypertriglyceridemia.Semantic proximity Read ↗

The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management.Semantic proximity Read ↗

Genetics of Hypertriglyceridemia.Semantic proximity Read ↗

Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.Semantic proximity Read ↗

Genetic bases of hypertriglyceridemic phenotypes.Semantic proximity Read ↗

Genetic basis of hypertriglyceridemies.Semantic proximity Read ↗

Integrating genetics and lifestyles for precision nutrition in hypertriglyceridemia: A UK Biobank and KoGES analysis.Semantic proximity Read ↗

Allelic and phenotypic spectrum of plasma triglycerides.Semantic proximity Read ↗

Clinical identification of familial chylomicronemia syndrome and novel therapeutic options.Semantic proximity Read ↗

Genetic and biochemical analysis of severe hypertriglyceridemia complicated with acute pancreatitis or with low post-heparin lipoprotein lipase mass.Semantic proximity Read ↗

Genetic determinants of pancreatitis: relevance in severe hypertriglyceridemiaSemantic proximity Read ↗

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