Evidence map›Paper›PMID 36741086›Full record

ArticleFrontiers in pediatrics2022

Case report: A

Xingxing Qiao, Liping Wu, Jianjun Tang, Rong Xiang, Liangliang Fan, Hao Huang, Yaqin Chen

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
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
0.6field-weighted citation impact, top 26% 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, 2 citations in OpenAlex.

  1. Frontiers in genetics · 2026
    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

7 authors at 4 institutions in 1 country.

Xingxing QiaoDepartment of Cardiology, Second Xiangya Hospital Central South University, Changsha, China.
Liping WuDepartment of Medical Genetics and Prenatal Diagnosis, Longgang District Maternity and Child Healthcare Hospital, Shenzhen, China.
Jianjun TangDepartment of Cardiology, Second Xiangya Hospital Central South University, Changsha, China.
Rong XiangDepartment of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
Liangliang FanDepartment of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
Hao HuangDepartment of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
Yaqin ChenDepartment of Cardiology, Second Xiangya Hospital Central South University, Changsha, China.
Central South University · CNSecond Xiangya Hospital of Central South University · CNShenzhen Maternity and Child Healthcare Hospital · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Campomelic dysplasia (CD) is an autosomal dominant skeletal dysplasia syndrome characterized by shortness and bowing of lower extremities, and often accompanied by XY sex reversal. Heterozygous pathogenic variants of Methods: We enrolled a Chinese family where the fetus was diagnosed with CD. The affected fetus was selected for whole-exome sequencing to identify the pathogenic mutations in this family. Results: After data filtering, a novel non-sense Conclusion: CD is a rare condition, which connected with

Indexed as

campomelic dysplasianon-senseSOX9terminated mutationtransactivation

Identifiers

PMID36741086
PMCPMC9890166
OpenAlexW4317106291

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.