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Article

Identification of Risk Pathways and Functional Modules for Coronary Artery Disease Based on Genome-wide SNP Data.

Genomics, proteomics & bioinformatics - 1 Dec 2016

Zhao Xiang, Luan Yi-Zhao, Zuo Xiaoyu, Chen Ye-Da, Qin Jiheng, Jin Lv, Tan Yiqing, Lin Meihua, Zhang Naizun, Liang Yan, Rao Shao-Qi

Abstract excerpt

Coronary artery disease (CAD) is a complex human disease, involving multiple genes and their nonlinear interactions, which often act in a modular fashion. Genome-wide single nucleotide polymorphism (SNP) profiling provides an effective technique to unravel these underlying genetic interplays or their functional involvements for CAD. This study aimed to identify the susceptible pathways and modules for CAD based...

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Identifiers

PMID: 27965104
DOI: 10.1016/j.gpb.2016.04.008
PMCID: PMC5200919

Genes

CAD

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.

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