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

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q.

American journal of human genetics - 1 Apr 2003

Pajukanta Päivi, Allayee Hooman, Krass Kelly L, Kuraishy Ali, Soro Aino, Lilja Heidi E, Mar Rebecca, Taskinen Marja-Riitta, Nuotio Ilpo, Laakso Markku, Rotter Jerome I, de Bruin Tjerk W A, Cantor Rita M, Lusis Aldons J, Peltonen Leena

Abstract excerpt

Several genomewide screens have been performed to identify novel loci predisposing to unfavorable serum lipid levels and coronary heart disease (CHD). We hypothesized that the accumulating data of these screens in different study populations could be combined to verify which of the identified loc...

Read the complete abstract on PubMed

Topics

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

Share to Cholesterol, HDL
Share to Chromosomes, Human, Pair 16

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Disease

Share to DNA, Satellite

Share to Germany

Share to Hyperlipidemia, Familial Combined

Share to Lod Score

Share to Netherlands

Source

Open in PubMed Open full text

Identifiers

PMID: 12638083
DOI: 10.1086/374177
PMCID: PMC1180353

Genes

FOXC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12638083-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q.PMID 12638083Read ↗

Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families.Semantic proximity Read ↗

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.Semantic proximity Read ↗

Genetics of familial combined hyperlipidemia and risk of coronary heart disease.Semantic proximity Read ↗

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.Semantic proximity Read ↗

Unraveling the complex genetics of familial combined hyperlipidemia.Semantic proximity Read ↗

The Contribution of GWAS Loci in Familial DyslipidemiasSemantic proximity Read ↗

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.Semantic proximity Read ↗

Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.Semantic proximity Read ↗

Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.Semantic proximity Read ↗

Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study.Semantic proximity Read ↗

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.Semantic proximity Read ↗

Genetics of familial combined hyperlipidemiaSemantic proximity Read ↗

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