Evidence map›Paper›PMID 35328096›Full record

ArticleGenes2022

Identification of Frameshift Variants in

Ghazala Y Zamani, Ranjha Khan, Noreen Karim, Zubair M Ahmed, Muhammad Naeem

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

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 3 countries.

Ghazala Y ZamaniMedical Genetics Research Laboratory, Department of Biotechnology, Quaid-i-Azam University, Islamabad 45320, Pakistan.
Ranjha KhanJoint Centre for Human Reproduction and Genetics, Anhui Society for Cell Biology, School of Life Sciences, University of Science and Technology of China, Hefei 230052, China.ORCID 0000-0002-1010-4407
Noreen KarimMedical Genetics Research Laboratory, Department of Biotechnology, Quaid-i-Azam University, Islamabad 45320, Pakistan.ORCID 0000-0002-5699-6500
Zubair M AhmedLaboratory of Neurogenetics and Translational Research, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0003-2914-4502
Muhammad NaeemMedical Genetics Research Laboratory, Department of Biotechnology, Quaid-i-Azam University, Islamabad 45320, Pakistan.ORCID 0000-0002-3894-3085
Quaid-i-Azam University · PKUniversity of Maryland, Baltimore · USUniversity of Science and Technology of China · CN

Funding

Molecular Determinants of Pigmentation (MDoP)R01AR077563 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Zubair M. Ahmed · 2021 to 2026
$2.4M
NIAMS NIH HHS R01 AR077563
6 · The paper itself

Abstract

Xeroderma pigmentosum (XP) is a rare autosomal recessive genetic disorder characterized by severe sensitivity of skin to sunlight and an increased risk of skin cancer. XP variant (XPV), a milder subtype, is caused by variants in the

Indexed as

Xeroderma PigmentosumAdultConsanguinityDNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA RepairHEK293 CellsHumansPakistanY-Family DNA PolymerasesDNA-Binding ProteinsDNA-Directed DNA PolymeraseRad30 proteinREV3L protein, humanY-Family DNA Polymerasesautosomal recessivePOLD2POLHpolymerase etaREV3LREV7xeroderma pigmentosum

Identifiers

PMID35328096
PMCPMC8955859
OpenAlexW4220671488

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.