Evidence map›Paper›PMID 37239044›Full record

ArticleBiomedicines2023

Association of Polymorphisms in

Eun-Ju Ko, Ji-Eun Shin, Jung-Yong Lee, Chang-Soo Ryu, Ji-Young Hwang, Young-Ran Kim, Eun-Hee Ahn, Ji-Hyang Kim, Nam-Keun Kim

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Mutation analysis of theTurkish journal of obstetrics and gynecology · 2026
    Article
  2. Review
  3. Review
  4. Association of Polymorphisms inDiagnostics (Basel, Switzerland) · 2024
    Article
  5. Article
  6. 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

9 authors at 2 institutions in 1 country.

Eun-Ju KoDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Republic of Korea.
Ji-Eun ShinDepartment of Obstetrics and Gynecology, Fertility Center of CHA Bundang Medical Center, CHA University, Seongnam 13520, Republic of Korea.
Jung-Yong LeeDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Republic of Korea.
Chang-Soo RyuDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Republic of Korea.
Ji-Young HwangDepartment of Obstetrics and Gynecology, Fertility Center of CHA Gangnam Medical Center, CHA University, Seoul 06125, Republic of Korea.ORCID 0000-0001-6895-7368
Young-Ran KimDepartment of Obstetrics and Gynecology, Fertility Center of CHA Bundang Medical Center, CHA University, Seongnam 13520, Republic of Korea.ORCID 0000-0001-8431-7563
Eun-Hee AhnDepartment of Obstetrics and Gynecology, Fertility Center of CHA Bundang Medical Center, CHA University, Seongnam 13520, Republic of Korea.
Ji-Hyang KimDepartment of Obstetrics and Gynecology, Fertility Center of CHA Bundang Medical Center, CHA University, Seongnam 13520, Republic of Korea.ORCID 0000-0002-9864-9777
Nam-Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Republic of Korea.ORCID 0000-0003-0541-3528
CHA University · KRCHA University Bundang Medical Center · KR

Funding

Korea Health Industry Development Institute HR22C1605National Research Foundation of Korea 2020R1F1A1074525National Research Foundation of Korea 2022R1F1A1064169National Research Foundation of Korea 2022R1F1A1074986
6 · The paper itself

Abstract

Recurrent implantation failure (RIF) refers to two or more unsuccessful in vitro fertilization embryo transfers in the same individual. Embryonic characteristics, immunological factors, and coagulation factors are known to be the causes of RIF. Genetic factors have also been reported to be involved in the occurrence of RIF, and some single nucleotide polymorphisms (SNPs) may contribute to RIF. We examined SNPs in

Indexed as

female hormonesgenotype combinationrecurrent implantation failuresingle-nucleotide polymorphism

Identifiers

PMID37239044
PMCPMC10216578
OpenAlexW4378515063

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.