Evidence map›Paper›PMID 30083359›Full record

ArticleHuman genome variation2018

A novel

Yoshika Akizawa, Toshiyuki Yamamoto, Kazuo Tamura, Toshiyuki Kanno, Nobuko Takahashi, Takeshi Ohki, Teppei Omori, Katsutoshi Tokushige, Masakazu Yamamoto, Kayoko Saito

Open access · goldAbstract readCase Reports
In one paragraph

Article in Human genome variation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. A Novel Splice-Site Mutation inFrontiers in oncology · 2020
    Article
  5. Article
  6. Review
  7. Current status of immunotherapy in metastatic colorectal cancer.International journal of colorectal disease · 2019
    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 1 country.

Yoshika Akizawa1Department of Obstetrics and Gynecology, Tokyo Women's Medical University, Tokyo, Japan.
Toshiyuki Yamamoto2Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.ORCID 0000-0002-9484-3505
Kazuo Tamura3Magor in Science, Graduate School of Science and Engineering Research, Kinki University, Higashiosaka, Japan.
Toshiyuki Kanno1Department of Obstetrics and Gynecology, Tokyo Women's Medical University, Tokyo, Japan.
Nobuko Takahashi1Department of Obstetrics and Gynecology, Tokyo Women's Medical University, Tokyo, Japan.
Takeshi Ohki4Department of Surgery, Institute of Gastroenterology, Tokyo Women's Medical University, Tokyo, Japan.ORCID 0000-0002-6328-0754
Teppei Omori5Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women's Medical University, Tokyo, Japan.
Katsutoshi Tokushige5Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women's Medical University, Tokyo, Japan.
Masakazu Yamamoto4Department of Surgery, Institute of Gastroenterology, Tokyo Women's Medical University, Tokyo, Japan.
Kayoko Saito2Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.
Tokyo Women's Medical University · JPKindai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lynch syndrome is a genetic disorder related to cancer predisposition, including colorectal cancer, endometrial cancer, and ovarian cancer. Germline mutations in mismatch repair genes, including

Identifiers

PMID30083359
PMCPMC6013486
OpenAlexW2809149029

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.