Evidence map›Paper›PMID 34447654›Full record

ArticleBalkan journal of medical genetics : BJMG2021

Association of

L Aidinidou, A Chatzikyriakidou, A Giannopoulos, V Karpa, I Tzimou, E Aidinidou, L Fidani

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

Article in Balkan journal of medical genetics : BJMG, 2021. 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. Review
  3. 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

7 authors at 2 institutions in 1 country.

L AidinidouDepartment of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
A ChatzikyriakidouDepartment of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
A GiannopoulosSecond Department of Pediatrics, Pediatric Cardiology Clinic, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
V KarpaDepartment of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
I TzimouSecond Department of Pediatrics, Pediatric Cardiology Clinic, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
E AidinidouDepartment of Microbiology, Health Center of Prinos, Thassos Island, Macedonia, Greece.
L FidaniDepartment of Medical Biology-Genetics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Aristotle University of Thessaloniki · GRAHEPA University Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital heart disease (CHD) is a group of structural defects of the heart and the great vessels, and one of the leading causes of death among infants and young adults. Several gene variants are involved in diverse mechanisms of cardiac and vessel development and could thus be considered candidate mutated genes for a congenital heart defect or a specific variant could predispose a person to CHD. In the present study, variants in four such genes are investigated for the first time in a group of young Greek CHD patients: the

Indexed as

Congenital heart disease (CHD)GATA4NFKB1 (–94ins/delATTG)NKX2-5RANKL

Identifiers

PMID34447654
PMCPMC8366470
OpenAlexW3186679239

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.