Evidence map›Paper›PMID 30027098›Full record

ArticleBioMed research international2018

Genetic Polymorphism in the

Haiyan Zhang, Zhuo Zhang, Linpei Jia, Wei Ji, Hai Li

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

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 1 country.

Haiyan ZhangDepartment of Gastrointestinal Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Zhuo ZhangDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Linpei JiaDepartment of Nephrology, Xuanwu Hospital of Capital Medical University, Beijing 100053, China.ORCID 0000-0003-0348-7814
Wei JiDepartment of Vascular Surgery, Jilin Provincial People's Hospital, Changchun 130000, China.
Hai LiDepartment of Urology, China-Japan Union Hospital of Jilin University, Changchun 130033, China.ORCID 0000-0002-0485-4981
Union Hospital · CNCapital Medical University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHypospadias is a common congenital malformation of the male external genitalia. Most cases have an unknown etiology, which is probably a mix of monogenic and multifactorial forms, implicating both genetic and environmental factors. Ryanodine receptor 1 (

methods263 congenital hypospadias children and 312 healthy children were recruited. The polymorphism of

resultsThe distribution frequencies of CC/CT/TT genotypes and two alleles (C and T) at

conclusionOur study demonstrated that

Indexed as

Gene FrequencyPolymorphism, Single NucleotideAsian PeopleCase-Control StudiesChildChild, PreschoolChinaFemaleGenetic Predisposition to DiseaseGenotypeHumansHypospadiasInfantMalePolymorphism, GeneticPregnancyRyanodine Receptor Calcium Release ChannelRYR1 protein, human

Identifiers

PMID30027098
PMCPMC6031201
OpenAlexW2809026151

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.