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Article

In-depth Mendelian randomization analysis of causal factors for coronary artery disease.

Scientific reports - 8 Jun 2020

Tan Yuan-De, Xiao Peng, Guda Chittibabu

Abstract excerpt

Selecting a set of valid genetic variants is critical for Mendelian randomization (MR) to correctly infer risk factors causing a disease. We here developed a method for selecting genetic variants as valid instrumental variables for inferring risk factors causing coronary artery disease (CAD). Using this method, we selected two sets of single-nucleotide-polymorphism (SNP) genetic variants (SNP338 and SNP363)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 32514076
DOI: 10.1038/s41598-020-66027-4
PMCID: PMC7280530

Genes

CAD
TG

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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