Evidence map›Paper›PMID 36387029›Full record

ArticleSaudi journal of biological sciences2023

Genetic heterogeneity of primary open-angle glaucoma in Pakistan.

Muhammad Yaqoob Shahani, Samreen Memon, Shakeel Ahmed Sheikh, Umbreen Bano, Pashmina Shaikh, Samina Gul Memon, Shazia Begum Shahani, Ikram Din Ujjan, Ashok Kumar Narsani, Ali Muhammad Waryah

Open access · hybridAbstract read
In one paragraph

Article in Saudi journal of biological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Analysis ofInternational journal of ophthalmology · 2024
    Article
  2. Review
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

10 authors at 1 institution in 1 country.

Muhammad Yaqoob ShahaniDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Samreen MemonDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Shakeel Ahmed SheikhDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Umbreen BanoDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Pashmina ShaikhDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Samina Gul MemonDepartment of Anatomy, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Shazia Begum ShahaniDepartment of Anatomy, Peoples' University of Medical & Health Sciences for Women, Shaheed Benazirabad, Pakistan.
Ikram Din UjjanDepartment of Pathology, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Ashok Kumar NarsaniInstitute of Ophthalmology, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Ali Muhammad WaryahMedical Research Centre, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.
Liaquat University of Medical & Health Sciences · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glaucoma is a neurodegenerative ophthalmic disorder and is considered among the leading causes of irreversible blindness. Primary open-angle glaucoma (POAG) is the most common type of glaucoma that affects after 30 years of life, progressing slowly, and manifests as decreased visual acuity leading to blindness if not treated. POAG is genetically heterogeneous, inherited most commonly in autosomal dominant mode. Several genes have been reported for POAG with myocilin ( Methods: After approval from Institutional Ethical Review Committee (ERC), 25 POAG families were enrolled from the southern province (Sindh) of Pakistan. Written informed consent was obtained from all participating individuals and diagnosis was confirmed by consultant ophthalmologists using various instruments and means. Venous blood was obtained from affected individuals and their normal family members for DNA extraction and subsequent analysis. Results: All samples were initially screened for the Conclusion: This is the first report of any POAG family found associated with a novel variant in

Indexed as

CYP1B1GlaucomaMyocilinPOAG

Identifiers

PMID36387029
PMCPMC9649946
OpenAlexW4307897451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.