Evidence map›Paper›PMID 31250579›Full record

ArticleYonsei medical journal2019

Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population.

Bingyang Li, Chongyu Hu, Junyu Liu, Xin Liao, Jiayu Xun, Manqian Xiao, Junxia Yan

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. A Rare Variant ofFrontiers in neurology · 2021
    Article
  5. Article
  6. Article
  7. 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 2 institutions in 1 country.

Bingyang Li *Department of Epidemiology and Health Statistics, XiangYa School of Public Health, Central South University, Hunan, China.ORCID https://orcid.org/0000-0003-0138-773X
Chongyu Hu *Department of Neurology, Hunan People's Hospital, Changsha, China.ORCID https://orcid.org/0000-0002-4086-0916
Junyu LiuDepartment of Neurosurgery, XiangYa Hospital, Central South University, Changsha, Hunan, China.ORCID https://orcid.org/0000-0002-3803-4068
Xin LiaoDepartment of Epidemiology and Health Statistics, XiangYa School of Public Health, Central South University, Hunan, China.ORCID https://orcid.org/0000-0002-9640-8638
Jiayu XunDepartment of Epidemiology and Health Statistics, XiangYa School of Public Health, Central South University, Hunan, China.ORCID https://orcid.org/0000-0002-9583-968X
Manqian XiaoDepartment of Epidemiology and Health Statistics, XiangYa School of Public Health, Central South University, Hunan, China.ORCID https://orcid.org/0000-0002-4844-3412
Junxia YanDepartment of Epidemiology and Health Statistics, XiangYa School of Public Health, Central South University, Hunan, China. 20457456@qq.com.ORCID https://orcid.org/0000-0001-6067-1613
Central South University · CNHunan Provincial People's Hospital · CN

Funding

Central South University 149946China postdoctoral science foundation 2015M582351
6 · The paper itself

Abstract

purposeGenome-wide association studies (GWAS) have revealed that common variants on or near MATERIALS AND

methodsA total of 765 individuals (including 230 IA patients and 535 controls) were involved in this study. Twelve single nucleotide polymorphisms (SNPs) of candidate loci were genotyped using the Sequenom MassARRAY platform. Associations were analyzed using univariate or multivariate logistic regression analysis.

resultsSNPs in

conclusionThese data partially confirmed earlier results and showed that variants in

Indexed as

Polymorphism, Single NucleotideAsian PeopleFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansIntracranial AneurysmMaleMiddle Agedgenetic polymorphismsIntracranial aneurysmsusceptibility genes

Identifiers

PMID31250579
PMCPMC6597466
OpenAlexW2954536941

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.