Evidence map›Paper›PMID 30555085›Full record

ArticleJournal of genetics2018

A novel study to examine the association of

S Reddy, Naindeep Kaur, Jagtar Singh

Abstract read
PubMed
In one paragraph

Article in Journal of genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. The Journal of international medical research · 2024
    Pooled it
  2. Frontiers in cardiovascular medicine · 2020
    Pooled it
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Variants ofDiagnostics (Basel, Switzerland) · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

S ReddyDepartment of Cardiology, Postgraduate Institute of Medical Education and Research, Chandigarh 160 012, India. reddycardio2911@gmail.com.
Naindeep Kaur
Jagtar Singh
Panjab University · INPost Graduate Institute of Medical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a drastic increase in the number of people suffering from coronary artery disease (CAD) worldwide with Indians being no exception. Being a developing country and experiencing a dramatic shift in lifestyle and eating habits, urbanization and industrialization, all these factors have collectively predisposed the Indian population towards CAD and the prevalence data arequite alarming. Genetic studies have disclosed the role of genes in CAD susceptibility and severity. One such gene is proprotein convertase subtilisin/kexin type 9 (

Indexed as

Polymorphism, Single NucleotideAllelesCase-Control StudiesCoronary Artery DiseaseGene FrequencyGenetic Predisposition to DiseaseGenetics, PopulationGenotypeHumansIndiaProprotein Convertase 9Risk FactorsPCSK9 protein, humanProprotein Convertase 9

Identifiers

PMID30555085
OpenAlexW2902703675

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.