Evidence map›Paper›PMID 36874343›Full record

ArticleCureus2023

STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.

Wannasiri Chiraphapphaiboon, Wanna Thongnoppakhun, Thawornchai Limjindaporn, Sunisa Sawasdichai, Ekkapong Roothumnong, Kanjana Prangphan, Benjaporn Pamornpol, Chanin Limwongse, Manop Pithukpakorn

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

Article in Cureus, 2023. 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
0.3field-weighted citation impact, top 44% 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, 1 citations in OpenAlex.

  1. Article
  2. Emerging insights intoTranslational lung cancer research · 2024
    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

9 authors at 2 institutions in 2 countries.

Wannasiri ChiraphapphaiboonDepartment of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Wanna ThongnoppakhunSiriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Thawornchai LimjindapornDepartment of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Sunisa SawasdichaiSiriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Ekkapong RoothumnongDivision of Medical Genetics, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Kanjana PrangphanSiriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Benjaporn PamornpolDepartment of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Chanin LimwongseSiriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Manop PithukpakornSiriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
ID Genomics (United States) · USSiriraj Hospital · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disorder caused by germline mutations in the serine-threonine kinase 11 (

Indexed as

copy number variationsdeletionsmutationspeutz-jeghers syndromestk11

Identifiers

PMID36874343
PMCPMC9983355
OpenAlexW4318816756

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.