Evidence map›Paper›PMID 28808579›Full record

ArticleHuman genome variation2017

A novel

Tatsuyuki Ohto, Takashi Enokizono, Ryuta Tanaka, Mai Tanaka, Hisato Suzuki, Aiko Sakai, Kazuo Imagawa, Hiroko Fukushima, Takashi Fukushima, Ryo Sumazaki and 3 more

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 24% 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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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.

Tatsuyuki OhtoDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID 0000-0002-5321-8869
Takashi EnokizonoDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Ryuta TanakaDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Mai TanakaDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Hisato SuzukiDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Aiko SakaiDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Kazuo ImagawaDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Hiroko FukushimaDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Takashi FukushimaDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Ryo SumazakiDepartment of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Tomoko UeharaCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Toshiki TakenouchiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Kenjiro KosakiCenter for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
University of Tsukuba · JPKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a 10-year-old girl with Bardet-Biedl syndrome caused by a novel mutation in the

Identifiers

PMID28808579
PMCPMC5550758
OpenAlexW2744361245

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.