Evidence map›Paper›PMID 35117658›Full record

ArticleTranslational cancer research2020

Analysis of a pedigree of Peutz-Jeghers syndrome and

Ling-Lin Tian, Jun-Zhi Guo, Yun-Qin Yin, Xiao-Hong Dang, Li-Juan Huo

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Translational cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 97% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Two missenseWorld journal of gastrointestinal oncology · 2024
    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

5 authors at 2 institutions in 1 country.

Ling-Lin TianDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Jun-Zhi GuoDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Yun-Qin YinDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Xiao-Hong DangDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Li-Juan HuoDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
First Hospital of Shanxi Medical University · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disorder characterised by gastrointestinal (GI) hamartomatous polyposis and mucocutaneous pigmentations. PJS is associated with an increased cancer risk, including GI and various extra-GI malignancies. In this study, we tracked this family for 8 years, and analyzed the clinical data of the PJS pedigree including two generations. In our research, the studied family members, including the proband, older daughter and younger daughter, all detected to have three heterozygous mutations in the

Indexed as

intussusceptionPeutz-Jeghers syndrome (PJS)RET proto-oncogene

Identifiers

PMID35117658
PMCPMC8797457
OpenAlexW3011776265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.