Evidence map›Paper›PMID 31218168›Full record

ArticleIntractable & rare diseases research2019

Splice receptor-site mutation c.697-2A>G of the

Naixiang Zhai, Yanqin Lu, Yanzhou Wang, Shie Zhang, Chuanming Peng, Shanshan Zhang, Tianyou Li, Mei Chen, Junlong Liu, Fengling Fang and 2 more

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

Article in Intractable & rare diseases research, 2019. 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
0.4field-weighted citation impact, top 31% 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. Case Report: A NovelFrontiers in genetics · 2021
    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

12 authors at 5 institutions in 2 countries.

Naixiang ZhaiSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Yanqin LuSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Yanzhou WangShandong Provincial Hospital Affiliated to Shandong First Medical University, Ji'nan, China.
Shie ZhangSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Chuanming PengSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Shanshan ZhangSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Tianyou LiShandong Provincial Hospital Affiliated to Shandong First Medical University, Ji'nan, China.
Mei ChenDepartment of Orthopaedic Surgery, The People's Hospital of Wuqing District, Tianjin, China.
Junlong LiuDepartment of Orthopaedic Surgery, The People's Hospital of Wuqing District, Tianjin, China.
Fengling FangDepartment of Orthopaedic Surgery, The People's Hospital of Wuqing District, Tianjin, China.
Xiuzhi RenDepartment of Orthopaedic Surgery, The People's Hospital of Wuqing District, Tianjin, China.
Jinxiang HanSchool of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Ji'nan, China.
Wuqing District People's Hospital · CNUniversity of Jinan · CNAcademy of Medical Sciences · GBShandong First Medical University · CNShandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility and blue sclerae, which are mainly caused by a mutation of the

Indexed as

COL1A1N-terminal of type I collagenOsteogenesis imperfectasplice receptor-site mutation

Identifiers

PMID31218168
PMCPMC6557241
OpenAlexW2952248098

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.