Evidence map›Paper›PMID 34526837›Full record

ArticleNoro psikiyatri arsivi2021

Investigation the Relationship of Autism Spectrum Disorder and

Sinem Yalçintepe, Işık Görker, Selma Demir, Emine İkbal Atli, Engin Atli, Hilmi Tozkir, Necdet Süt, Yasemin Özen, Damla Eker, Çisem Mail and 3 more

Open access · greenAbstract read
In one paragraph

Article in Noro psikiyatri arsivi, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Iron dysregulation in the central nervous system: implications for autism spectrum disorder.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    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

13 authors at 1 institution in 1 country.

Sinem Yalçintepe1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Işık GörkerTrakya University Faculty of Medicine, Department of Child and Adolescent Psychiatry, Edirne, Turkey.
Selma Demir1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Emine İkbal Atli1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Engin Atli1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Hilmi Tozkir1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Necdet SütTrakya University Faculty of Medicine, Department of Biostatistics and Medical Informatics, Edirne, Turkey.
Yasemin Özen1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Damla Eker1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Çisem Mail1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Hazal Sezginer Güler1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Drenushe Zhuri1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Hakan Gurkan1Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey.
Trakya University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAutism spectrum disorder is a genetically and phenotypically heterogeneous group. Genetic studies carried out to date have suggested that both common and rare genetic variants play a role in the etiology of this disorder. In our study, we aimed to investigate the effect of

methodIn our prospectively planned study, all exons and exon-intron junctions of

resultsIn our study, the average age was 10.1 and the male/female ratio was 75/21. Pathogenic or likely pathogenic variants were not detected in

conclusionIn our study, we could not identify a relationship between the autism spectrum disorder and

Indexed as

Autism spectrum disorderFOXP2GABRA4GRIN2BKATNAL2Next generation sequencing

Identifiers

PMID34526837
PMCPMC8419723
OpenAlexW3135303913

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.