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Article

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.

Clinical genetics - 1 Mar 2017

Ram R, Wakil S M, Muiya N P, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer B F, Morahan G, Dzimiri N

Abstract excerpt

Hypertriglyceridemia (hTG) is a lipid disorder, resulting from an elevation in triglyceride levels, with a strong genetic component. It constitutes a significant risk factor for coronary artery disease (CAD), a leading cause of death worldwide. In this study, we performed a common variant association study for hTG in ethnic Saudi Arabs. We genotyped 5501 individuals in a two-phase experiment using Affymetrix...

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Source

Identifiers

PMID: 27599772
DOI: 10.1111/cge.12859

Genes

APOA1
APOA5
CAD
GCKR
LAMC1
MLXIPL

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.

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