Evidence map›Paper›PMID 36980825›Full record

SynthesisGenes2023

Pathogenicity Analysis of a Novel Variant in

Qin Zhang, Qianqian Ouyang, Jingjing Xiang, Hong Li, Haitao Lv, Yu An

Open access · goldFull text readSystematic ReviewCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Synthesis in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. A novel mutation inHeliyon · 2024
    Article
  4. Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcome.Annals of clinical and translational neurology · 2024
    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

6 authors at 3 institutions in 1 country.

Qin ZhangDepartment of Cardiology, Children's Hospital of Soochow University, Suzhou 215127, China.
Qianqian OuyangHuman Phenome Institute, Zhangjiang Fudan International Innovation Center, MOE Key Laboratory of Contemporary Anthropology, Fudan University, Shanghai 201203, China.ORCID 0000-0002-6414-3049
Jingjing XiangCenter for Reproduction and Genetics, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou 215008, China.
Hong LiCenter for Reproduction and Genetics, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou 215008, China.
Haitao LvDepartment of Cardiology, Children's Hospital of Soochow University, Suzhou 215127, China.
Yu AnHuman Phenome Institute, Zhangjiang Fudan International Innovation Center, MOE Key Laboratory of Contemporary Anthropology, Fudan University, Shanghai 201203, China.ORCID 0000-0001-8051-8229
Fudan University · CNSoochow University · CNSuzhou Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defect of

Indexed as

GTP-Binding ProteinsMitochondrial DiseasesChildChild, PreschoolHumansHyperlactatemiaInfantMaleSeizuresGTP-Binding ProteinsGTPBP3 protein, humanCOXPD23GTPBP3mitochondrial diseasestaurine modificationvariants

Identifiers

PMID36980825
PMCPMC10048406
OpenAlexW4321598600

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read2
measurements read26
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.