Evidence map›Paper›PMID 35898556›Full record

ArticlePharmacogenomics and personalized medicine2022

Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.

Safiah Alhazmi, Maryam Alzahrani, Reem Farsi, Mona Alharbi, Khloud Algothmi, Najla Alburae, Magdah Ganash, Sheren Azhari, Fatemah Basingab, Asma Almuhammadi and 7 more

Open 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. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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  4. Research square · 2026
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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

17 authors at 3 institutions in 1 country.

Safiah AlhazmiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-0755-4498
Maryam AlzahraniDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Reem FarsiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Mona AlharbiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Khloud AlgothmiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Najla AlburaeDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Magdah GanashDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Sheren AzhariDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Fatemah BasingabDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Asma AlmuhammadiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Amany AlqosaibiDepartment of Biology, Imam Abdulrahman bin Faisal University, Dammam, Saudi Arabia.ORCID 0000-0001-8348-9451
Heba AlkhatabiCentre of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.
Aisha ElaimiCentre of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-3214-4714
Mohammed JanCollege of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Hesham M AldhalaanCenter for Autism Research at King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Aziza AlrafiahDepartment of Medical Laboratory Science, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-0978-5775
Aisha AlrofaidiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0002-0416-2723
King Abdulaziz University · SAImam Abdulrahman Bin Faisal University · SAKing Faisal Specialist Hospital & Research Centre · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Autism spectrum disorder (ASD) is a developmental disorder that can cause substantial social, communication, and behavioral challenges. Genetic factors play a significant role in ASD, where the risk of ASD has been increased for unclear reasons. Twin studies have shown important evidence of both genetic and environmental contributions in ASD, where the level of contribution of these factors has not been proven yet. It has been suggested that copy number variation (CNV) duplication and the deletion of many genes in chromosome 22 (Ch22) may have a strong association with ASD. This study screened the CNVs in Ch22 in autistic Saudi children and assessed the candidate gene in the CNVs region of Ch22 that is most associated with ASD. Methods: This study included 15 autistic Saudi children as well as 4 healthy children as controls; DNA was extracted from samples and analyzed using array comparative genomic hybridization (aCGH) and DNA sequencing. Results: The aCGH detected (in only 6 autistic samples) deletion and duplication in many regions of Ch22, including some critical genes. Moreover, DNA sequencing determined a genetic mutation in the TBX1 gene sequence in autistic samples. This study, carried out using aCGH, found that six autistic patients had CNVs in Ch22, and DNA sequencing revealed mutations in the TBX1 gene in autistic samples but none in the control. Conclusion: CNV deletion and the duplication of the TBX1 gene could be related to ASD; therefore, this gene needs more analysis in terms of expression levels.

Indexed as

autism spectrum disorderchromosome 22copy number variationsSaudi autistic childrenTBX1

Identifiers

PMID35898556
PMCPMC9309317
OpenAlexW4288046774

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.