Evidence map›Paper›PMID 32514154›Full record

ArticleScientific reports2020

A heritable profile of six miRNAs in autistic patients and mouse models.

Yusuf Ozkul, Serpil Taheri, Kezban Korkmaz Bayram, Elif Funda Sener, Ecmel Mehmetbeyoglu, Didem Behice Öztop, Fatma Aybuga, Esra Tufan, Arslan Bayram, Nazan Dolu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Article
  5. Article
  6. Journal of clinical practice and research · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Autism-RelatedBiomolecules · 2024
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

16 authors at 5 institutions in 2 countries.

Yusuf OzkulErciyes University Medical Faculty, Medical Genetics Department, Kayseri, Turkey. ozkul@erciyes.edu.tr.
Serpil TaheriErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Kezban Korkmaz BayramErciyes University Medical Faculty, Medical Genetics Department, Kayseri, Turkey.
Elif Funda SenerErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Ecmel MehmetbeyogluErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Didem Behice ÖztopAnkara University, Medical Faculty, Child and Adolescent Psychiatry Department, Ankara, Turkey.
Fatma AybugaErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Esra TufanErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Arslan BayramErciyes University Medical Faculty, Medical Genetics Department, Kayseri, Turkey.ORCID http://orcid.org/0000-0002-3682-2140
Nazan DoluBaskent University, Medical Faculty, Physiology Department, Ankara, Turkey.
Gokmen ZararsizErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey.
Leila KianmehrUniversité Côte d'Azur, CNRS, Inserm, France.
Feyzullah BeyazErciyes University Veterinary Faculty, Histology and Embryology Department, Kayseri, Turkey.ORCID http://orcid.org/0000-0002-9365-4104
Züleyha DoganyigitBozok University, Medical Faculty, Histology and Embryology Department, Yozgat, Turkey.
François CuzinUniversité Côte d'Azur, CNRS, Inserm, France.
Minoo RassoulzadeganErciyes University, Betul-Ziya Eren Genome and Stem Cell Center, Kayseri, Turkey. minoo@unice.fr.ORCID http://orcid.org/0000-0002-5522-0647
Erciyes University · TRCentre National de la Recherche Scientifique · FRAnkara University · TRBaşkent University · TRYozgat Bozok Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a group of developmental pathologies that impair social communication and cause repetitive behaviors. The suggested roles of noncoding RNAs in pathology led us to perform a comparative analysis of the microRNAs expressed in the serum of human ASD patients. The analysis of a cohort of 45 children with ASD revealed that six microRNAs (miR-19a-3p, miR-361-5p, miR-3613-3p, miR-150-5p, miR-126-3p, and miR-499a-5p) were expressed at low to very low levels compared to those in healthy controls. A similar but less pronounced decrease was registered in the clinically unaffected parents of the sick children and in their siblings but never in any genetically unrelated control. Results consistent with these observations were obtained in the blood, hypothalamus and sperm of two of the established mouse models of ASD: valproic acid-treated animals and Cc2d1a

Indexed as

Gene Expression ProfilingAdolescentAdultAnimalsAnxietyAutism Spectrum DisorderAutistic DisorderChildChild, PreschoolDepressionDisease Models, AnimalEarly DiagnosisExploratory BehaviorFemaleHumansHypothalamusCc2d1a protein, mouseMicroRNAsRepressor ProteinsValproic Acid

Identifiers

PMID32514154
PMCPMC7280218
OpenAlexW3033894798

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.