Evidence map›Paper›PMID 31572550›Full record

ArticleExperimental and therapeutic medicine2019

Clinical application of chromosome 9p21.3 genotyping in patients with coronary artery disease.

Svetlana Nikulina, Ivan Artyukhov, Pavel Shesternya, Oksana Gavrilyuk, Vladimir Maksimov, Mikhail Voyevoda, Denis Brusentsov

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Experimental and therapeutic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

7 authors at 1 institution in 1 country.

Svetlana NikulinaDepartment of Internal Diseases No. 1, Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University of The Ministry of Healthcare of The Russian Federation, Krasnoyarsk 660022, Russian Federation.
Ivan ArtyukhovDepartment of Internal Diseases No. 1, Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University of The Ministry of Healthcare of The Russian Federation, Krasnoyarsk 660022, Russian Federation.
Pavel ShesternyaDepartment of Internal Diseases No. 1, Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University of The Ministry of Healthcare of The Russian Federation, Krasnoyarsk 660022, Russian Federation.
Oksana GavrilyukDepartment of Internal Diseases No. 1, Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University of The Ministry of Healthcare of The Russian Federation, Krasnoyarsk 660022, Russian Federation.
Vladimir MaksimovLaboratory of Molecular Genetic Studies of Therapeutic Diseases, Institute of Internal and Preventive Medicine of The Siberian Branch of The Russian Academy of Medical Sciences, Novosibirsk 630089, Russian Federation.
Mikhail VoyevodaLaboratory of Molecular Genetic Studies of Therapeutic Diseases, Institute of Internal and Preventive Medicine of The Siberian Branch of The Russian Academy of Medical Sciences, Novosibirsk 630089, Russian Federation.
Denis BrusentsovDepartment of Internal Diseases No. 1, Professor V.F. Voino-Yasenetsky Krasnoyarsk State Medical University of The Ministry of Healthcare of The Russian Federation, Krasnoyarsk 660022, Russian Federation.
Krasnoyarsk State Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to investigate the susceptibility of two coronary artery disease (CAD)-associated single nucleotide polymorphisms on 9p21 (

Indexed as

cardiogeneticsclinical application of genomic datamyocardial infarctionpercutaneous coronary interventionprevention

Identifiers

PMID31572550
PMCPMC6755495
OpenAlexW2967562310

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.