Evidence map›Paper›PMID 37799141›Full record

ArticleFrontiers in genetics2023

Prospect of genetic disorders in Saudi Arabia.

Amerh S Alqahtani, Raniah S Alotibi, Taghrid Aloraini, Fahad Almsned, Yara Alassali, Ahmed Alfares, Bader Alhaddad, Mariam M Al Eissa

Abstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

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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

8 authors.

Amerh S AlqahtaniMedical Genetics Department, King Saud Medical City, Riyadh, Saudi Arabia.
Raniah S AlotibiDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, King Abdullah International Medical Research Centre (KAIMRC), Riyadh, Saudi Arabia.
Taghrid AlorainiDivision of Translational Pathology, Department of Laboratory Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Fahad AlmsnedResearch Centre, King Fahad Specialist Hospital in Dammam (KFSH-D), Dammam, Saudi Arabia.
Yara AlassaliMedical School, AlFaisal University, Riyadh, Saudi Arabia.
Ahmed AlfaresCentre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Bader AlhaddadMolecular Genetics Department, King Saud Medical City, Riyadh, Saudi Arabia.
Mariam M Al EissaPublic Health Authority, Public Health Lab, Molecular Genetics Laboratory, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

diagnostic yieldexome sequencinggenome sequencingneurodevelopmental disorderspanelSaudi Arabiasingle nucleotide variant

Identifiers

PMID37799141
PMCPMC10548463

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.