Evidence map›Paper›PMID 42358636›Full record

ArticleFrontiers in cardiovascular medicine2026

Rare pathogenic mutation of

Yubi Lin, Xingchen Li, Mingsui Gao, Yechang Chen, Zhuguo Wu, Jia Chen

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in cardiovascular medicine, 2026. 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

6 authors.

Yubi Lin *The Dongguan TaiXin Hospital, Affiliated to Guangdong Medical University, Dongguan, China.
Xingchen Li *The Dongguan TaiXin Hospital, Affiliated to Guangdong Medical University, Dongguan, China.
Mingsui GaoThe Second Department of Cardiology, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou, China.
Yechang ChenThe First Dongguan Affiliated Hospital, Guangdong Medical University, Dongguan, China.
Zhuguo WuThe First Dongguan Affiliated Hospital, Guangdong Medical University, Dongguan, China.
Jia ChenThe Second Department of Cardiology, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Long QT syndrome (LQTS) is a life-threatening inherited channelopathy that is prone to triggering torsades de pointes (TdP), ventricular tachycardia (VT), ventricular fibrillation (VF), and sudden cardiac death. Materials and methods: Whole-exome sequencing (WES) was performed on a proband with LQTS, and candidate variants were validated by Sanger sequencing. Bioinformatics methods were used to analyze the pathogenicity of the variants. Results: A proband who was a 16-year-old girl presented with a prolonged QT interval, TdP, VT, and VF. She carried the Conclusions: The

Indexed as

KCNH2long QT syndromeventricular arrhythmiavoltage-sensing domainwhole-exome sequencing

Identifiers

PMID42358636
PMCPMC13290691

What OpenQuestion holds

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Registered trials

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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.