Evidence map›Paper›PMID 35174115›Full record

ArticleFrontiers in pediatrics2021

Andersen-Tawil Syndrome With Novel Mutation in

Jisook Yim, Kyoung Bo Kim, Minsun Kim, Gun Dong Lee, Myungshin Kim

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

Article in Frontiers in pediatrics, 2021. 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
0.3field-weighted citation impact, top 46% 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, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. The network of cardiac KNaunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  4. Chronic Propafenone Application Increases Functional KPharmaceuticals (Basel, Switzerland) · 2023
    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

5 authors at 2 institutions in 1 country.

Jisook YimDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Kyoung Bo KimDepartment of Laboratory Medicine, Keimyung University School of Medicine, Daegu, South Korea.
Minsun KimDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Gun Dong LeeDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Myungshin KimDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
The Catholic University of Korea Seoul St. Mary's Hospital · KRKeimyung University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Andersen-Tawil syndrome (ATS) is a rare autosomal dominant disorder characterized by a classic symptom triad: periodic paralysis, ventricular arrhythmias associated with prolonged QT interval, and dysmorphic skeletal and facial features. Pathogenic variants of the inwardly rectifying potassium channel subfamily J member 2 (KCNJ2) gene have been linked to the ATS. Herein, we report a novel

Indexed as

Andersen–Tawil syndromedysmorphic featuregenetic disorderKCNJ2 geneKIR2.1long QT syndromeperiodic paralysispotassium channel

Identifiers

PMID35174115
PMCPMC8842678
OpenAlexW4210789793

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.