Evidence map›Paper›PMID 35003222›Full record

ArticleFrontiers in genetics2021

Polymorphisms Within DNA Double-Strand Breaks Repair-Related Genes Contribute to Structural Chromosome Abnormality in Recurrent Pregnancy Loss.

Zhenbo Cheng, Dehua Cheng, Jiancheng Li, Lihuang Guo, Wei Zhang, Conghui Zhang, Yangxu Liu, Yue Huang, Keqian Xu

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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 3 institutions in 1 country.

Zhenbo ChengDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Dehua ChengSchool of Basic Medical Science, Institute of Reproductive and Stem Cell Engineering, Central South University, Changsha, China.
Jiancheng LiDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Lihuang GuoDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Wei ZhangDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Conghui ZhangDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Yangxu LiuDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Yue HuangDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Keqian XuDepartment of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CNReproductive & Genetic Hospital CITIC-Xiangya · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DNA double-strand breaksEP300gene polymorphismsnon-homologous end joiningrecurrent pregnancy lossstructural chromosome abnormalitieswhole-exome sequencing

Identifiers

PMID35003222
PMCPMC8733605
OpenAlexW4200300703

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.