Evidence map›Paper›PMID 33082985›Full record

ArticleHuman genome variation2020

Jervell and Lange-Nielsen syndrome with novel KCNQ1 and additional gene mutations.

Shinichi Matsuda, Yuko Ohnuki, Mayuri Okami, Eriko Ochiai, Shiro Yamada, Kazumi Takahashi, Motoki Osawa, Kenji Okami, Masahiro Iida, Hiroyuki Mochizuki

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

Article in Human genome variation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. [Congenital long QT syndrome].Archivos peruanos de cardiologia y cirugia cardiovascular
    Review
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

10 authors at 2 institutions in 2 countries.

Shinichi MatsudaDepartment of Pediatrics, Tokai University School of Medicine, Isehara, Japan.
Yuko OhnukiDepartment of Medical Ethics, Tokai University School of Medicine, Isehara, Japan.
Mayuri OkamiDepartment of Clinical Genetics, Tokai University Hospital, Isehara, Japan.
Eriko OchiaiDepartment of Forensic Medicine, Tokai University School of Medicine, Isehara, Japan.
Shiro YamadaDepartment of Pediatrics, Tokai University Oiso Hospital, Oiso, Japan.ORCID 0000-0003-3370-0065
Kazumi TakahashiDepartment of Medical Ethics, Tokai University School of Medicine, Isehara, Japan.
Motoki OsawaDepartment of Forensic Medicine, Tokai University School of Medicine, Isehara, Japan.
Kenji OkamiDepartment of Otolaryngology, Tokai University School of Medicine, Isehara, Japan.
Masahiro IidaDepartment of Otolaryngology, Tokai University School of Medicine, Isehara, Japan.
Hiroyuki MochizukiDepartment of Pediatrics, Tokai University School of Medicine, Isehara, Japan.
Tokai University · JPShonan Oiso Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We encountered a boy with Jervell and Lange-Nielsen syndrome (JLNS) with compound heterozygous

Indexed as

Disease geneticsGenetic counselling

Identifiers

PMID33082985
PMCPMC7562699
OpenAlexW3093977514

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.