Evidence map›Paper›PMID 34093671›Full record

ArticleFrontiers in genetics2021

Case Report: A Novel Heterozygous

Yongzhe Chen, Zesong Wang, Yueren Wu, Wenbin He, Juan Du, Sufen Cai, Fei Gong, Guangxiu Lu, Ge Lin, Can Dai

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 2021. 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
2.2field-weighted citation impact, top 13% 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, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Advances in the genetic etiology of female infertility.Journal of assisted reproduction and genetics · 2024
    Review
  7. A heterozygousiScience · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Novel mutations in ZP2 and ZP3 cause female infertility in three patients.Journal of assisted reproduction and genetics · 2022
    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

10 authors at 4 institutions in 1 country.

Yongzhe ChenSchool of Basic Medical Science, Central South University, Changsha, China.
Zesong WangDepartment of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
Yueren WuDepartment of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
Wenbin HeReproductive and Genetic Hospital of China International Trust Investment Corporation Xiangya, Changsha, China.
Juan DuSchool of Basic Medical Science, Central South University, Changsha, China.
Sufen CaiSchool of Basic Medical Science, Central South University, Changsha, China.
Fei GongSchool of Basic Medical Science, Central South University, Changsha, China.
Guangxiu LuDepartment of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
Ge LinSchool of Basic Medical Science, Central South University, Changsha, China.
Can DaiDepartment of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
Hunan Provincial Center for Disease Control and Prevention · CNHunan Normal University · CNCentral South University · CNCITIC Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

empty follicle syndromefemale infertilityfollicular developmentzona pellucidaZP3 mutation

Identifiers

PMID34093671
PMCPMC8170154
OpenAlexW3159976661

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.