Evidence map›Paper›PMID 28881593›Full record

ArticleOncotarget2017

Association of genetic polymorphisms in

Maowei Xie, Daofa Zhang, Yin Zhang, Xiaohong Yang, Yan Su, Yanni Wang, Haiyang Huang, Hui Han, Wenning Li, Keying Fu and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Frontiers in genetics · 2021
    Article
  5. The Impacts ofInternational journal of general medicine · 2021
    Article
  6. The association of genetic polymorphisms in interleukin-1 receptors type 1 and type 2 with age-related hearing impairment in a Taiwanese population: a case control study.Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale · 2020
    Article
  7. IL1R1 Polymorphisms are Associated with Lumbar Disc Herniation Risk in the Northwestern Chinese Han Population.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. 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

13 authors at 1 institution in 1 country.

Maowei Xie *Department of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Daofa Zhang *Department of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Yin Zhang *Department of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Xiaohong YangDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Yan SuDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Yanni WangDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Haiyang HuangCentral Laboratory, Hainan General Hospital, Haikou Hainan 570311, China.
Hui HanDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Wenning LiDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Keying FuCentral Laboratory, Hainan General Hospital, Haikou Hainan 570311, China.
Huiluan SuDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Wentan XuDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Jiali WeiDepartment of Nephrology, Hainan General Hospital, Haikou Hainan 570311, China.
Hainan General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimIgA nephropathy (IgAN) is the major cause of end-stage renal disease(ESRD) in Asia and its pathogenesis is influenced by both genetic and environmental factors. Single nucleotide polymorphisms (SNPs) in

resultIn the allelic model analysis, the rs10490571 and rs3917225 were associated with a 1.40-fold, and 1.31-fold increased risk of IgA nephropathy, respectively. In the genetic model analysis, the rs10490571 in MATERIALS AND

methodsA case-control study was conducted including 426 nephropathy patients and 463 healthy controls. Chi-squared tests and genetic model were used to evaluate associations. >

conclusionsThese findings suggested that

Indexed as

Chinese Han populationgenetics polymorphismIgA nephropathyIL-1R1IL-1R2

Identifiers

PMID28881593
PMCPMC5584187
OpenAlexW2604197535

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.