Evidence map›Paper›PMID 35860328›Full record

ArticleFrontiers in bioengineering and biotechnology2022

Identification of a Novel Heterozygous Mutation in the

Yun Tian, Qiong Liu, Yafang Zhou, Xiao-Yu Chen, Yongcheng Pan, Hongwei Xu, Zhuanyi Yang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 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
0.8field-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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

7 authors at 2 institutions in 1 country.

Yun TianDepartment of Geriatrics, Xiangya Hospital, Central South University, Changsha, China.
Qiong LiuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Yafang ZhouDepartment of Geriatrics, Xiangya Hospital, Central South University, Changsha, China.
Xiao-Yu ChenDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Yongcheng PanDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Hongwei XuDepartment of Geriatrics, Xiangya Hospital, Central South University, Changsha, China.
Zhuanyi YangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vanishing white matter disease (VWM) is one of the most common childhood inherited leukoencephalopathies with autosomal recessive inheritance. Mutations in five genes,

Indexed as

EIF2B4heterozygous missense mutationloss of functiontargeted gene capture sequencing panelvanishing white matter disease

Identifiers

PMID35860328
PMCPMC9289103
OpenAlexW4283803676

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.