Evidence map›Paper›PMID 29082893›Full record

ArticleJournal of clinical research in pediatric endocrinology2018

One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the

Xiang Chen, Huijun Wang, Bingbing Wu, Xinran Dong, Bo Liu, Hongbo Chen, Yulan Lu, Wenhao Zhou, Lin Yang

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  5. 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

9 authors at 1 institution in 1 country.

Xiang ChenChildren’s Hospital of Fudan University, Clinic of Neonatology, Shanghai, China
Huijun WangChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Bingbing WuChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Xinran DongChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Bo LiuChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Hongbo ChenChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Yulan LuChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Wenhao ZhouChildren’s Hospital of Fudan University, Clinic of Neonatology, Shanghai, China
Lin YangChildren’s Hospital of Fudan University, Key Laboratory of Birth Defects, Shanghai, China
Children's Hospital of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the insulin receptor (

Indexed as

Antigens, CDChinaDonohue SyndromeHumansInfant, NewbornInfant, Newborn, DiseasesMaleMutationReceptor, InsulinAntigens, CDINSR protein, humanReceptor, InsulinInsulin receptor genemutationneonatenext generation sequencingRabson-Mendenhall syndrome

Identifiers

PMID29082893
PMCPMC5985390
OpenAlexW2765287349

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.