Evidence map›Paper›PMID 35221709›Full record

ArticlePharmacogenomics and personalized medicine2022

DNA Methylation Level of Transcription Factor Binding Site in the Promoter Region of Acyl-CoA Synthetase Family Member 3 (

Khloud Algothmi, Amal Alqurashi, Aisha Alrofaidi, Mona Alharbi, Reem Farsi, Najla Alburae, Magdah Ganash, Sheren Azhari, Fatemah Basingab, Asma Almuhammadi and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 60% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Khloud AlgothmiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Amal AlqurashiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Aisha AlrofaidiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0002-0416-2723
Mona AlharbiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Reem FarsiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Najla AlburaeBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Magdah GanashBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Sheren AzhariBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Fatemah BasingabBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Asma AlmuhammadiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Amany AlqosaibiDepartment of Biology, College of Science, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.ORCID 0000-0001-8348-9451
Heba AlkhatabiKing Abdulaziz University, Centre of Excellence in Genomic Medicine Research, Jeddah, Saudi Arabia.
Aisha ElaimiKing Abdulaziz University, Centre of Excellence in Genomic Medicine Research, Jeddah, Saudi Arabia.ORCID 0000-0003-3214-4714
Mohammed JanCollege of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Hesham AldhalaanCenter for Autism Research at King Faisal Specialist Hospital & Research Center (KFSH & RC), Riyadh, Saudi Arabia.
Aziza AlrafiahMedical LaboratorySciencesDepartment,Faculty of Applied Medical Sciences, Jeddah, Saudi Arabia.ORCID 0000-0003-0978-5775
Safiah AlhazmiBiological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-0755-4498
King Abdulaziz University · SAImam Abdulrahman Bin Faisal University · SAKing Faisal Specialist Hospital & Research Centre · SAUniversity of Jeddah · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA methylation (DNAm) is one of the main epigenetic mechanisms that affects gene expression without changing the underlying DNA sequence. Aberrant DNAm has an implication in different human diseases such as cancer, schizophrenia, and autism spectrum disorder (ASD). ASD is a neurodevelopmental disorder that affects behavior, learning, and communication skills. Acyl-CoA synthetase family member 3 (

methodsRT-qPCR and DNA methylight qPCR were used to determine the expression and DNAm level in the promoter region of

resultsThe results showed a significant correlation between the gene expression of

conclusionAlthough this study found no DNAm in the binding site of

Indexed as

ACSF3autismDNAmDNA methylationSaudi autistic childrenSP1

Identifiers

PMID35221709
PMCPMC8865760
OpenAlexW4213367304

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.