Evidence map›Paper›PMID 37470043›Full record

ArticleFrontiers in genetics2023

A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss.

Na Liao, Zhu Zhang, Xijing Liu, Jiamin Wang, Rui Hu, Like Xiao, Yunyuan Yang, Yi Lai, Hongmei Zhu, Lingping Li and 3 more

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

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Na LiaoDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Zhu ZhangDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Xijing LiuDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Jiamin WangDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Rui HuDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Like XiaoDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Yunyuan YangDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Yi LaiDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Hongmei ZhuDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Lingping LiDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Shanling LiuDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
He WangDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Ting HuDepartment of Medical Genetics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
West China Second University Hospital of Sichuan University · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

chromosomal abnormalitychromosomal microarray analysiscopy-number variationfirst trimestermiscarriagepregnancy lossproducts of conceptionuniparental disomy

Identifiers

PMID37470043
PMCPMC10352453
OpenAlexW4382722657

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.