Evidence map›Paper›PMID 33083304›Full record

ArticleIranian journal of public health2020

Association of Genetic Polymorphisms in

Sima Shahrokhzadeh, Azam Soleimani, Dor-Mohammad Kordi-Tamandani, Mohammad Hossein Sangtarash, Omid Nejati, Mohsen Taheri

Open access · goldAbstract read
In one paragraph

Article in Iranian journal of public health, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 3 institutions in 1 country.

Sima ShahrokhzadehDepartment of Biology, University of Sistan and Baluchestan, Zahedan, Iran.
Azam SoleimaniLegal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.
Dor-Mohammad Kordi-TamandaniDepartment of Biology, University of Sistan and Baluchestan, Zahedan, Iran.
Mohammad Hossein SangtarashDepartment of Biology, University of Sistan and Baluchestan, Zahedan, Iran.
Omid NejatiDepartment of Paramedics, Mashhad Medical Sciences Branch, Islamic Azad University, Mashhad, Iran.
Mohsen TaheriGenetics of Non-Communicable Diseases Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.
University of Sistan and Baluchestan · IRIranian Legal Medicine Organization · IRZahedan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVesicoureteral reflux (VUR) disease is the most common type of urinary tract anomalies in children. Genetic risk factors may be associated with the etiology of VUR. The role of the Glutathione S-transferases (

methodsThe study was done in 2013 in Sistan and Baluchestan University, eastern Iran. Genotyping of three

resultsThe presence of

conclusionDeletion of

Indexed as

Genetic polymorphismsGenetic susceptibilityGlutathione S-transferaseVesicoureteral reflux

Identifiers

PMID33083304
PMCPMC7548483
OpenAlexW3037813913

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.