Evidence map›Paper›PMID 34200157›Full record

ArticleInternational journal of molecular sciences2021

Genetic Polymorphisms in

Sung-Hwan Cho, Ji-Hyang Kim, Hui-Jeong An, Young-Ran Kim, Eun-Hee Ahn, Jung-Ryeol Lee, Jung-Oh Kim, Jung-Jae Ko, Nam-Keun Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. The effect of MicroRNAs variants on idiopathic recurrent pregnancy loss.Journal of assisted reproduction and genetics · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. 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

9 authors at 4 institutions in 1 country.

Sung-Hwan ChoDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Ji-Hyang KimCHA Bundang Medical Center, Department of Obstetrics and Gynecology, School of Medicine, CHA University, Seongnam 13496, Korea.ORCID 0000-0002-9864-9777
Hui-Jeong AnDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Young-Ran KimCHA Bundang Medical Center, Department of Obstetrics and Gynecology, School of Medicine, CHA University, Seongnam 13496, Korea.
Eun-Hee AhnCHA Bundang Medical Center, Department of Obstetrics and Gynecology, School of Medicine, CHA University, Seongnam 13496, Korea.
Jung-Ryeol LeeDepartment of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam 13488, Korea.ORCID 0000-0003-3743-2934
Jung-Oh KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.ORCID 0000-0002-4171-2034
Jung-Jae KoDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Nam-Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.ORCID 0000-0003-0541-3528
CHA University Bundang Medical Center · KRCHA University · KRGangneung–Wonju National University · KRSeoul National University Bundang Hospital · KR

Funding

Korea Health Industry Development Institute HI18C19990200National Research Foundation of Korea NRF-2018R1D1A1B07047604National Research Foundation of Korea NRF-2020R1I1A1A01060656
6 · The paper itself

Abstract

The purpose of this study was to investigate whether polymorphisms in five microRNAs (miRNAs),

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single Nucleotide3' Untranslated RegionsAbortion, HabitualAdultCase-Control StudiesEmbryo ImplantationFemaleGenetic Association StudiesGenotypeHumansMicroRNAsPregnancy3' Untranslated RegionsMicroRNAsMIRN938 microRNA, humanGnRHRmicroRNAMTHFRrecurrent pregnancy losssingle nucleotide polymorphism (SNP)

Identifiers

PMID34200157
PMCPMC8201216
OpenAlexW3166292677

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.