Evidence mapPaperPMID 35510247Full record

ArticleFrontiers in medicine2022

Genetic Association of rs1021188 and DNA Methylation Signatures of

Amal Bouzid, Ameni Chelly, Adel Tekari, Neha Singh, Kirtal Hansdah, Imen Achour, Ikhlas Ben Ayed, Fida Jbeli, Ilhem Charfeddine, Puppala Venkat Ramchander and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. 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
0.3field-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, 4 citations in OpenAlex.

  1. SOD mediates mitochondrial epigenetic regulation in NIHL.Frontiers in cellular neuroscience · 2025
    Article
  2. 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 4 countries.

Amal BouzidSharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Ameni ChellyLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Adel TekariLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Neha SinghInstitute of Life Sciences, Nalco Square, Bhubaneswar, India.
Kirtal HansdahInstitute of Life Sciences, Nalco Square, Bhubaneswar, India.
Imen AchourDepartment of Otorhinolaryngology, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
Ikhlas Ben AyedMedical Genetic Department, University Hedi Chaker Hospital of Sfax, Sfax, Tunisia.
Fida JbeliLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Ilhem CharfeddineDepartment of Otorhinolaryngology, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
Puppala Venkat RamchanderInstitute of Life Sciences, Nalco Square, Bhubaneswar, India.
Rifat HamoudiSharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Saber MasmoudiLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
University of Sfax · TNInstitute of Life Sciences · INCentre of Biotechnology of Sfax · TNHopital Universitaire Hedi Chaker · TNUniversity College London · GBUniversity of Sharjah · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Otosclerosis (OTSC) is a complex bone disorder of the otic capsule, which causes conductive hearing impairment in human adults. The dysregulation of the signaling axis mediated by the receptor activator of nuclear factor-kappa-B (RANK), RANK ligand (RANKL), and osteoprotegerin has been widely attributed to the context of metabolic bone disorders. While genetic associations and epigenetic alterations in the

Indexed as

bone remodelingDNA methylationhearing lossotosclerosisrs1021188TNFSF11

Identifiers

PMID35510247
PMCPMC9058115
OpenAlexW4223932697

What Socratic 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 Socratic graph.