Evidence map›Paper›PMID 28546864›Full record

ArticleHuman genome variation2017

The first Japanese case of central precocious puberty with a novel

Junko Nishioka, Hirohito Shima, Maki Fukami, Shuichi Yatsuga, Takako Matsumoto, Kikumi Ushijima, Miyuki Kitamura, Yasutoshi Koga

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

Article in Human genome variation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Genetic causes of central precocious puberty.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2022
    Review
  2. Article
  3. Review
  4. Makorin RING finger protein 3 and central precocious puberty.Current opinion in endocrine and metabolic research · 2020
    Article
  5. Article
  6. Article
  7. Review
  8. Journal of the Endocrine Society · 2019
    Article
  9. (Epi)genetic defects ofHuman genome variation · 2019
    Article
  10. 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

8 authors at 2 institutions in 1 country.

Junko NishiokaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Hirohito ShimaDepartment of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Maki FukamiDepartment of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Shuichi YatsugaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Takako MatsumotoDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Kikumi UshijimaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Miyuki KitamuraDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Yasutoshi KogaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Kurume University · JPNational Center For Child Health and Development · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID28546864
PMCPMC5435957
OpenAlexW2616759532

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.