Evidence map›Paper›PMID 36196359›Full record

ArticleNeuropsychiatric disease and treatment2022

Genetic Polymorphism of NQO1 Gene is Associated with Susceptibility of Ischemic Stroke in Chinese Han Nationality.

Limin Yan, Dedong Xu, Ying Xiao, Mingming Dai, Ting Wang, Xinhong Zhuang, Kunliang Wu

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Impact of NQO1 dysregulation in CNS disorders.Journal of translational medicine · 2024
    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

7 authors at 1 institution in 1 country.

Limin Yan *Department of Neurology, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Dedong Xu *Department of Neurosurgery, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Ying XiaoDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Mingming DaiDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Ting WangDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Xinhong ZhuangDepartment of Nephrology, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Kunliang WuDepartment of Infectious Diseases, The Second Affiliated Hospital of Hainan Medical University, Haikou, People's Republic of China.
Hainan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: NAD(P)H: Quinone Oxidoreductase 1 gene (NQO1) polymorphism is associated with the risk of cardiovascular disease. This study was designed to investigate the relationship between NQO1 gene polymorphism and ischemic stroke susceptibility in Chinese Han nationality. Patients and Methods: One hundred and forty-one patients diagnosed with ischemic stroke and 139 matched control groups were recruited in this study. The polymorphism distribution of Results: The frequency distribution of the three genotypes of NQO1 Conclusion: The NQO1

Indexed as

genetic polymorphismischemic strokeNQO1oxidized low-density lipoprotein

Identifiers

PMID36196359
PMCPMC9527027
OpenAlexW4297537202

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.