Evidence map›Paper›PMID 36428936›Full record

ArticleDiagnostics (Basel, Switzerland)2022

A Novel Deletion Mutation of the F8 Gene for Hemophilia A.

Jingwei Wang, Jian Gu, Hongbing Chen, Qian Wu, Liang Xiong, Bin Qiao, Yan Zhang, Hongjun Xiao, Yongqing Tong

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

Article in Diagnostics (Basel, Switzerland), 2022. 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 28% 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, 4 citations in OpenAlex.

  1. Review
  2. Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

9 authors at 1 institution in 1 country.

Jingwei WangDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID 0000-0003-3337-4386
Jian GuDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Hongbing ChenDepartment of Pulmonary and Critical Care Medicine of Renmin Hospital, Wuhan University, Wuhan 430060, China.
Qian WuClinical Molecular Diagnosis Institute, Wuhan University, Wuhan 430060, China.
Liang XiongDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Bin QiaoDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Yan ZhangDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Hongjun XiaoMedical Vocational and Technical School, Wuhan University, Wuhan 430060, China.
Yongqing TongDepartment of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Wuhan University · CN

Funding

Guidance Fund from Hubei Provincial Natural Science Foundation 2020KZ00741Guidance Fund Project of Renmin hospital of Wuhan University RMYD2018M76Innovation Project funding from Wuhan university school of medicine TFZZ2018015
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

bleeding disordercoagulation factor FVIIIgene mutationhemophilia A

Identifiers

PMID36428936
PMCPMC9689134
OpenAlexW4309740762

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.