Evidence map›Paper›PMID 36676722›Full record

ArticleMedicina (Kaunas, Lithuania)2022

Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family.

Muhammad Ajmal, Hafsah Muhammad, Muhammad Nasir, Muhammad Shoaib, Salman Akbar Malik, Irfan Ullah

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2022. 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
0.7field-weighted citation impact, top 28% 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, 4 citations in OpenAlex.

  1. Article
  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

6 authors at 4 institutions in 1 country.

Muhammad AjmalInstitute of Biomedical and Genetic Engineering, 24-Mauve area, G-9/1, Islamabad 44000, Pakistan.
Hafsah MuhammadDepartment of Molecular Biology and Genetics, Institute of Basic Medical Science, Faculty of Basic Medical Sciences, Khyber Medical University, Phase V Hayatabad, Peshawar 25000, Pakistan.ORCID 0000-0002-5501-3920
Muhammad NasirInstitute of Biomedical and Genetic Engineering, 24-Mauve area, G-9/1, Islamabad 44000, Pakistan.
Muhammad ShoaibKRL General Hospital, Orthopaedic Department 24-Mauve area, G-9/1 Islamabad 44000, Pakistan.
Salman Akbar MalikDepartment of Biochemistry, Quaid-i-Azam University, Islamabad 44000, Pakistan.
Irfan UllahDepartment of Life Sciences, School of Science, University of Management and Technology (UMT), Lahore 54770, Pakistan.ORCID 0000-0001-6992-6723
Institute of Biomedical and Genetic Engineering · PKKhyber Medical University · PKQuaid-i-Azam University · PKUniversity of Management and Technology · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Exostoses, Multiple HereditaryAmino AcidsHaploinsufficiencyHedgehog ProteinsHeparan SulfateHumansMutationN-AcetylglucosaminyltransferasesPakistanAmino AcidsHedgehog ProteinsHeparan SulfateN-AcetylglucosaminyltransferasesEXT1EXT2haploinsufficiencyheparan-sulfatehereditary multiple exostoses

Identifiers

PMID36676722
PMCPMC9863873
OpenAlexW4313427584

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.