Evidence map›Paper›PMID 40881174›Full record

ArticleFrontiers in genetics2025

Genetic analysis of non-syndromic peg lateralis using whole-exome sequencing.

Junglim Choi, Sungnam Kim, Hyunsoo Ahn, Donghyo Kim, Sung-Won Cho, Sanguk Kim, Jae Hoon Lee

Abstract read
In one paragraph

Article in Frontiers in genetics, 2025. 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
–field-weighted citation impact
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. Article
  2. MSX1 and PAX9 Polymorphisms and Their Association With Lateral Incisor Morphology in Patients With Maxillary Canine Impaction.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Observational
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

7 authors.

Junglim Choi *Department of Advanced General Dentistry, School of Dentistry, Dankook University, Cheonan-si, Chungcheongnam-do, Republic of Korea.
Sungnam Kim *Department of Life Sciences, Pohang University of Science and Technology, Pohang-si, Gyeongsangbuk-do, Republic of Korea.
Hyunsoo AhnGraduate School of Artificial Intelligence, Pohang University of Science and Technology, Pohang-si, Gyeongsangbuk-do, Republic of Korea.
Donghyo KimDepartment of Chemical Engineering, Pohang University of Science and Technology, Pohang-si, Gyeongsangbuk-do, Republic of Korea.
Sung-Won ChoDivision of Anatomy and Developmental Biology, Department of Oral Biology, BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, Republic of Korea.
Sanguk KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang-si, Gyeongsangbuk-do, Republic of Korea.
Jae Hoon LeeDepartment of Prosthodontics, Yonsei University College of Dentistry, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Although peg-shaped lateral incisors are a common dental anomaly, the genetic mechanisms governing peg lateralis are poorly understood, particularly in cases where other associated anomalies are absent. Here, we aimed to identify potential candidate genes contributing to the development of non-syndromic peg lateralis via whole-exome sequencing (WES). Methods: Saliva samples were collected from 20 unrelated Korean individuals with non-syndromic peg lateralis. WES was conducted on these samples, and variants with Results: We identified a heterozygous allele for Conclusion: The results suggest a possible function of these newly identified genes in the development of peg lateralis, which remains to be defined. This study may provide new insights into the genetic basis of non-syndromic peg lateralis, establishing a basis for the further analysis of the disease-associated genes identified herein.

Indexed as

calcium fluxdental anomaliesgenetic analysisnon-syndromic peg lateralisOTOP1RP11-131H24.4whole-exome sequencing

Identifiers

PMID40881174
PMCPMC12380783

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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.