Evidence map›Paper›PMID 32695431›Full record

ArticleHuman genome variation2020

Molecular diagnosis of an infant with

Keita Osumi, Kenichi Suga, Akemi Ono, Aya Goji, Tatsuo Mori, Yukiko Kinoshita, Mikio Sugano, Yoshihiro Toda, Maki Urushihara, Ryuji Nakagawa and 3 more

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

13 authors at 2 institutions in 1 country.

Keita OsumiDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.ORCID 0000-0003-4268-9988
Kenichi SugaDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Akemi OnoDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Aya GojiDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Tatsuo MoriDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Yukiko KinoshitaDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Mikio SuganoDepartment of Cardiovascular Surgery, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima, Japan.
Yoshihiro TodaDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Maki UrushiharaDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Ryuji NakagawaDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Yasunobu HayabuchiDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.ORCID 0000-0001-6143-2673
Issei ImotoDepartment of Preventive Medicine, Division of Molecular Genetics, Aichi Cancer Center Research Institute, Nagoya, Aichi Japan.
Shoji KagamiDepartment of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Tokushima Japan.
Tokushima University Hospital · JPAichi Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 1-month-old Japanese infant with cardiac rhabdomyoma was diagnosed with

Indexed as

Genetic testingPolycystic kidney disease

Identifiers

PMID32695431
PMCPMC7363882
OpenAlexW3042310745

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.