Evidence map›Paper›PMID 37635800›Full record

ArticleFrontiers in pediatrics2023

Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the

Nengqing Liu, Xiaojun Wen, Zhanhui Ou, Xiaowu Fang, Jing Du, Xiufeng Lin

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Nengqing LiuReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Xiaojun WenReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Zhanhui OuReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Xiaowu FangReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Jing DuReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Xiufeng LinReproductive Center, Zhongshan Boai Hospital, Zhongshan, China.
Boai Hospital of Zhongshan · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-Linked Alport Syndrome (XLAS) is an X-linked, dominant, hereditary nephropathy mainly caused by mutations in the

Indexed as

COL4A5next-generation sequencingpreimplantation genetic testingtype IV collagenX-Linked alport syndrome

Identifiers

PMID37635800
PMCPMC10448762
OpenAlexW4385719973

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.