Evidence map›Paper›PMID 37892645›Full record

ArticleJournal of clinical medicine2023

Exploring the Genetic Causes for Postnatal Growth Failure in Children Born Non-Small for Gestational Age.

Yoo-Mi Kim, Han-Hyuk Lim, Eunhee Kim, Geena Kim, Minji Kim, Hyejin So, Byoung Kook Lee, Yoowon Kwon, Jeesu Min, Young Seok Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 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
0.8field-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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Monogenic causes of familial short stature.Frontiers in endocrinology · 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

10 authors at 1 institution in 1 country.

Yoo-Mi KimDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.ORCID 0000-0002-8440-5069
Han-Hyuk LimDepartment of Pediatrics, School of Medicine, Chungnam National University, Daejeon 34134, Republic of Korea.
Eunhee KimDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.
Geena KimDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.ORCID 0000-0002-6837-7475
Minji KimDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.ORCID 0000-0001-5588-5414
Hyejin SoDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.
Byoung Kook LeeDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.
Yoowon KwonDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.ORCID 0000-0002-9249-7493
Jeesu MinDepartment of Pediatrics, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.ORCID 0000-0003-1535-7769
Young Seok LeeDepartment of Radiology, Chungnam National University Sejong Hospital, Sejong 30099, Republic of Korea.
Chungnam National University · KR

Funding

National Research Foundation of Korea grant funded by the Korean government Ministry of Science and ICT No.2018R1C1B5086428
6 · The paper itself

Abstract

The most common causes of short stature (SS) in children are familial short stature (FSS) and idiopathic short stature (ISS). Recently, growth plate dysfunction has been recognized as the genetic cause of FSS or ISS. The aim of this study was to investigate monogenic growth failure in patients with ISS and FSS. Targeted exome sequencing was performed in patients categorized as ISS or FSS and the subsequent response to growth hormone (GH) therapy was analyzed. We found 17 genetic causes involving 12 genes (

Indexed as

exome sequencinggenetic diseasesgrowth hormonenon-small for gestational ageshort stature

Identifiers

PMID37892645
PMCPMC10607479
OpenAlexW4387614507

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.