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

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population.

Journal of human genetics - 1 May 2016

Konta Atsuko, Ozaki Kouichi, Sakata Yasuhiko, Takahashi Atsushi, Morizono Takashi, Suna Shinichiro, Onouchi Yoshihiro, Tsunoda Tatsuhiko, Kubo Michiaki, Komuro Issei, Eishi Yoshinobu, Tanaka Toshihiro

Abstract excerpt

Coronary artery disease (CAD) including myocardial infarction is one of the leading causes of death in many countries. Similar to other common diseases, its pathogenesis is thought to result from complex interactions among multiple genetic and environmental factors. Recent large-scale genetic association analysis for CAD identified 15 new loci. We examined the reproducibility of these previous association...

Read the complete abstract on PubMed

Topics

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

Share to Risk
Share to Comorbidity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Artery Disease

Share to Gene Knockdown Techniques

Share to Genetic Loci

Share to Reproducibility of Results

Share to Vascular Endothelial Growth Factor Receptor-1

Source

Identifiers

PMID: 26791355
DOI: 10.1038/jhg.2015.171

Genes

FLT1
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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population.PMID 26791355Read ↗

The Effect of FLT1 Variant on Long-Term Cardiovascular Outcomes: Validation of a Locus Identified in a Previous Genome-Wide Association Study.Semantic proximity Read ↗

A genome-wide association study of a coronary artery disease risk variant.Semantic proximity Read ↗

Genetic variants of VEGFR-1 gene promoter in acute myocardial infarction.Semantic proximity Read ↗

Fibroblast growth factor receptor 4 polymorphisms and coronary artery disease: a case control study.Semantic proximity Read ↗

FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.Semantic proximity Read ↗

Genetic variant in the 3'-untranslated region of VEGFR1 gene influences chronic obstructive pulmonary disease and lung cancer development in Chinese population.Semantic proximity Read ↗

Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.Semantic proximity Read ↗

Genetic Variation in NFKB1 and NFKBIA and Susceptibility to Coronary Artery Disease in a Chinese Uygur Population.Semantic proximity Read ↗

Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report.Semantic proximity Read ↗

Fibroblast growth factor receptor 4 polymorphisms and susceptibility to coronary artery disease.Semantic proximity Read ↗

Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease.Semantic proximity Read ↗

Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population.Semantic proximity Read ↗

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