Evidence map›Paper›PMID 35211766›Full record

ArticleMolecular medicine reports2022

Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT‑2 gene deletion mutation.

Wentao Wang, Mingyuan Yang, Yuhang Shen, Kai Chen, Donghua Wu, Changwei Yang, Jinyi Bai, Dawei He, Jun Gao

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

9 authors at 2 institutions in 1 country.

Wentao Wang *Department of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Mingyuan Yang *Department of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Yuhang Shen *Department of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Kai Chen *Department of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Donghua WuDepartment of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Changwei YangDepartment of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Jinyi BaiDepartment of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Dawei HeDepartment of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Jun GaoDepartment of Orthopedics, Shanghai Changhai Hospital, Shanghai 200433, P.R. China.
Second Military Medical University · CNChanghai Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to report a clinical survey of hereditary multiple exostoses (HME) in a large Chinese pedigree, and the identification of a novel deletion mutation of exostosin glycosyltransferase 2 (

Indexed as

Exostoses, Multiple HereditaryChinaExostosin 2FemaleGene DeletionHumansMaleMutationN-AcetylglucosaminyltransferasesPedigreeExostosin 2N-Acetylglucosaminyltransferasesclinical surveyDNA sequencinghereditary multiple exostosespathogenesis

Identifiers

PMID35211766
PMCPMC8915398
OpenAlexW4213445001

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.