Enduring mystery of the chromosome 9p21.3 locus.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

6 citing papers in PubMed.

1. What Causes Premature Coronary Artery Disease?Current atherosclerosis reports · 2024
   Review
2. Analysis of ANRIL Isoforms and Key Genes in Patients with Severe Coronary Artery Disease.International journal of molecular sciences · 2023
   Article
3. Association between Coronary Artery Disease and rs10757278 and rs1333049 Polymorphisms in 9p21 Locus in Iran.Reports of biochemistry & molecular biology · 2020
   Article
4. The 9p21.3 risk locus for coronary artery disease: A 10-year search for its mechanism.Journal of Taibah University Medical Sciences · 2017
   Review
5. Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.Human genetics · 2014
   Article
6. Genetic insights into cardiometabolic risk factors.The Clinical biochemist. Reviews · 2014
   Review

Corrections and comments

• Comment on
  9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response.2011
• Comment on
  Interferon-γ activates expression of p15 and p16 regardless of 9p21.3 coronary artery disease risk genotype.2013

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.