Evidence map›Paper›PMID 36833437›Full record

ArticleGenes2023

A Novel Homozygous Nonsense Variant in the

Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque and 2 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Observational
  2. Article
  3. 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

12 authors at 6 institutions in 3 countries.

Abu BakarDepartment of Biochemistry, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.ORCID 0000-0001-9331-3468
Sulaiman ShamsDepartment of Biochemistry, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.ORCID 0000-0001-7792-1180
Nousheen BibiDepartment of Bioinformatics, Shaheed Benazir Bhutto Women University, Peshawar 25120, Pakistan.
Asmat UllahNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0002-5715-3425
Wasim AhmadDepartment of Biochemistry, Quaid-I-Azam University, Islamabad 45320, Pakistan.
Musharraf JelaniRare Diseases Genetics and Genomics, Centre for Omic Sciences, Islamia College Peshawar, Peshawar 25120, Pakistan.ORCID 0000-0002-3421-0079
Osama Yousef MuthaffarDepartment of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-3458-1697
Angham Abdulrhman AbdulkareemFaculty of Science, Department of Biochemistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Turki S AbujamelDepartment of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Absarul HaqueDepartment of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Muhammad Imran NaseerCenter of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Bushra KhanDepartment of Biochemistry, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.ORCID 0000-0002-3239-496X
King Abdulaziz University · SAAbdul Wali Khan University Mardan · PKIslamia College University · PKQuaid-i-Azam University · PKShaheed Benazir Bhutto Women University Peshawar · PKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: Dyggve-Melchior-Clausen Syndrome is a skeletal dysplasia caused by a defect in the

Indexed as

DwarfismIntellectual DisabilityOsteochondrodysplasiasHumansIntracellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsDyggve-Melchior-Clausen SyndromeDYM genehomozgosity mappingnon-sense variantnovel homozygoussanger sequencing

Identifiers

PMID36833437
PMCPMC9956627
OpenAlexW4321248230

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.