Evidence map›Paper›PMID 31827649›Full record

ArticleDisease markers2019

Analysis of Polymorphisms Associated with Base Excision Repair in Patients Susceptible and Resistant to Noise-Induced Hearing Loss.

Enmin Ding, Jiadi Guo, Xin Ge, Rongjian Sheng, Jian Chen, Hengdong Zhang, Baoli Zhu

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

Article in Disease markers, 2019. 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
0.4field-weighted citation impact, top 43% 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. [Research progress in genetics of noise-induced hearing loss].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2024
    Review
  2. Review
  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

7 authors at 3 institutions in 1 country.

Enmin DingJiangsu Provincial Center for Disease Prevention and Control, Institute of Occupational Disease Prevention, Nanjing, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-3805-1386
Jiadi GuoCenter for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-6584-2215
Xin GeYizheng Hospital, Drum Tower Hospital Group of Nanjing, Yizheng, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-0773-8556
Rongjian ShengYizheng Hospital, Drum Tower Hospital Group of Nanjing, Yizheng, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-5516-3590
Jian ChenYizheng Hospital, Drum Tower Hospital Group of Nanjing, Yizheng, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-8401-0166
Hengdong ZhangJiangsu Provincial Center for Disease Prevention and Control, Institute of Occupational Disease Prevention, Nanjing, Jiangsu Province, China.
Baoli ZhuCenter for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-4345-0154
Nanjing Drum Tower Hospital · CNJiangsu Provincial Center for Disease Control and Prevention · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveNoise-induced hearing loss (NIHL) is one of the most common occupational health risks in both developed and industrialized countries. It occurs as a result of interactions between genetic and environmental factors. Nevertheless, inherited genetic factors contributing to NIHL are not well understood. Therefore, we aim to investigate whether genetic mutations in three important base excision repair genes (

methodsThree SNPs in

resultsResults showed that the rs1799782 TT genotype located in the

conclusions

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAsian PeopleCase-Control StudiesDNA-(Apurinic or Apyrimidinic Site) LyaseDNA GlycosylasesFemaleFollow-Up StudiesGenotypeHearing Loss, Noise-InducedHumansMaleOccupational ExposurePrognosisX-ray Repair Cross Complementing Protein 1APEX1 protein, humanDNA-(Apurinic or Apyrimidinic Site) LyaseDNA Glycosylasesoxoguanine glycosylase 1, humanX-ray Repair Cross Complementing Protein 1XRCC1 protein, human

Identifiers

PMID31827649
PMCPMC6885169
OpenAlexW2983455086

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.