Evidence map›Paper›PMID 36467473›Full record

ArticleFrontiers in pediatrics2022

Case report: A novel mutation in

Qi Huang, Cheng Jiang, Jiazhong Sun, Junli Xue, Victor Wei Zhang

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Review
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

5 authors at 3 institutions in 1 country.

Qi HuangDepartment of Endocrinology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Cheng JiangEmergency Center, Zhongnan Hospital of Wuhan University, Wuhan, China.
Jiazhong SunDepartment of Endocrinology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Junli XueDepartment of Endocrinology, The Second Clinical Medical College, Yangtze University, Jingzhou, China.
Victor Wei ZhangDepartment of Clinical Genetics, AmCare Genomics Lab, Guangzhou, China.
Zhongnan Hospital of Wuhan University · CNWuhan University · CNYangtze University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tricho-rhino-phalangeal syndrome (TRPS) is a rare autosomal dominant malformation caused by mutations involving the

Indexed as

deletion mutationshort staturesparse hairtricho-Rhino-Phalangeal syndromeTRPS1 gene

Identifiers

PMID36467473
PMCPMC9716017
OpenAlexW4309271129

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.