Evidence map›Paper›PMID 36873675›Full record

ArticleIntractable & rare diseases research2023

Type XV osteogenesis imperfecta: A novel mutation in the

Jicai Zhu, Kai Liu, Shan He, Zihao Yang, Jiaying Song, Yan Ju, Caiyun Xiong, Guomei Zhang, Wen Yang, Chunhui Tang

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

Article in Intractable & rare diseases research, 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
0.6field-weighted citation impact, top 25% 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

10 authors at 2 institutions in 1 country.

Jicai ZhuDepartment of Pediatrics, The First People's Hospital of Yunnan Province, Medical School & Affiliated Hospital, Kunming University of Science and Technology, Kunming, Yunnan, China.
Kai LiuDepartment of Pediatrics, The First People's Hospital of Yunnan Province, Medical School & Affiliated Hospital, Kunming University of Science and Technology, Kunming, Yunnan, China.
Shan HeDepartment of Pediatrics, The First People's Hospital of Yunnan Province, Medical School & Affiliated Hospital, Kunming University of Science and Technology, Kunming, Yunnan, China.
Zihao YangMedical School & Affiliated Hospital, Kunming University of Science and Technology. Department of Radiology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Jiaying SongMedical School & Affiliated Hospital, Kunming University of Science and Technology. Department of Pediatrics, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Yan JuMedical School & Affiliated Hospital, Kunming University of Science and Technology. Department of Pediatrics, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Caiyun XiongMedical School & Affiliated Hospital, Kunming University of Science and Technology. Department of Pediatrics, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Guomei ZhangDepartment of Pediatrics, The First People's Hospital of Yunnan Province, Medical School & Affiliated Hospital, Kunming University of Science and Technology, Kunming, Yunnan, China.
Wen YangMedical School & Affiliated Hospital, Kunming University of Science and Technology. Department of Pediatrics, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Chunhui TangDepartment of Pediatrics, The First People's Hospital of Yunnan Province, Medical School & Affiliated Hospital, Kunming University of Science and Technology, Kunming, Yunnan, China.
First People's Hospital of Yunnan Province · CNKunming University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Wnt signaling pathway is vital in encouraging bone growth.

Indexed as

heterozygous mutationinner ear dysplasiatype XV osteogenesis imperfectaWNT1

Identifiers

PMID36873675
PMCPMC9976088
OpenAlexW4317643320

What OpenQuestion holds

Textmetadata
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.