Evidence map›Paper›PMID 35281812›Full record

ArticleFrontiers in genetics2022

Case Report: Biventricular Noncompaction Cardiomyopathy With Pulmonary Stenosis and Bradycardia in a Fetus With KCNH2 Mutation.

Hairui Sun, Xiaowei Liu, Xiaoyan Hao, Xiaoxue Zhou, Jingyi Wang, Jiancheng Han, Mengmeng Liang, Hongjia Zhang, Yihua He

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

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Zebrafish in Cardiovascular Disease Research: from Model to Application.International journal of biological sciences · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. 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 3 institutions in 1 country.

Hairui SunDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xiaowei LiuDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xiaoyan HaoDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Xiaoxue ZhouDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jingyi WangDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jiancheng HanDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Mengmeng LiangCipher Gene LLC, Beijing, China.
Hongjia ZhangDepartment of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Yihua HeDepartment of Echocardiography, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Beijing Anzhen Hospital · CNCapital Medical University · CNCipher Gene (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

congenital heart diseaseKCNH2 gene mutationleft ventricular noncompactionlong QT syndromeprenatal diagnosis

Identifiers

PMID35281812
PMCPMC8908010
OpenAlexW4214648406

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.