Evidence map›Paper›PMID 33082981›Full record

ArticleHuman genome variation2020

A novel

Junpei Hamada, Fumihiro Ochi, Yuka Sei, Koji Takemoto, Hiroki Hirai, Misa Honda, Hironori Shibata, Tomonobu Hasegawa, Mariko Eguchi

Open access · goldAbstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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.

Junpei HamadaDepartment of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan.ORCID 0000-0002-1852-3278
Fumihiro OchiDepartment of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan.
Yuka SeiDepartment of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan.
Koji TakemotoDepartment of Pediatrics, Ehime Prefectural Niihama Hospital, Ehime, Japan.
Hiroki HiraiDepartment of Pediatrics, Ehime Prefectural Central Hospital, Ehime, Japan.
Misa HondaDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Hironori ShibataDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Tomonobu HasegawaDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Mariko EguchiDepartment of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan.ORCID 0000-0001-8727-1732
Ehime University · JPKeio University · JPEhime Prefectural Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the first case of Waardenburg syndrome type 4C and Kallmann syndrome in the same person. The patient, a Japanese girl, presented with bilateral iris depigmentation, bilateral sensorineural hearing loss, Hirschsprung disease, hypogonadotropic hypogonadism, and anosmia. We identified a novel

Indexed as

Disease geneticsHypogonadism

Identifiers

PMID33082981
PMCPMC7522263
OpenAlexW3090797648

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.