Evidence map›Paper›PMID 39653367›Full record

ArticleGenetic testing and molecular biomarkers2024

Detection of Genetic Variations in Children with Tetralogy of Fallot Using Whole Exome Sequencing Technology Integrated Bioinformatics Analysis.

Khalid Mohamoud Abdullahi, Ahmed Faisal Ali, Mohamed Mohamoud Adan, Qiang Shu

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genetic testing and molecular biomarkers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Khalid Mohamoud AbdullahiDepartment of Cardiac Surgery, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, No. 3333 Binsheng Road, Hangzhou, China.ORCID 0009-0009-4164-6629
Ahmed Faisal AliDepartment of Infectious Disease, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Mohamed Mohamoud AdanDepartment of Urology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Qiang ShuDepartment of Cardiac Surgery, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, No. 3333 Binsheng Road, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Exome SequencingGenetic VariationTetralogy of FallotChildChild, PreschoolComputational BiologyEast Asian PeopleExomeFemaleGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansInfantInfant, NewbornMaleMutationcongenital heart diseasegenetic varianttetralogy of fallotwhole exome sequencing

Identifiers

PMID39653367
PMCPMC11659463

What Socratic 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 Socratic graph.