Evidence map›Paper›PMID 39320561›Full record

ReviewHuman genetics2024

Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.

Youmei Wu, Ling Lai, Junyang Chen, Xinzhu Li, Jin Hou

Abstract readReview
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In one paragraph

Review in Human genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Genes · 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.

Youmei WuDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Ling LaiDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Junyang ChenDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Xinzhu LiDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Jin HouDepartment of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China. houjin@smu.edu.cn.

Funding

National Natural Science Foundation of China NO. 81971902
6 · The paper itself

Abstract

Tooth agenesis (TA) occurs when tooth development is disrupted at the initiation stage. It can be classified into non-syndromic and syndromic forms (named NSTA and STA), depending on whether it is accompanied by abnormalities of other organs and systems. Genetic factors play a predominant role in the pathogenesis of tooth agenesis, with dozens of genes implicated in both forms. Several genes have been identified, mutations in which can lead to both forms of TA. Among these, WNT10A and EDA are frequently mutated genes in this context, representing extensively researched and documented genes in human non-syndromic selective agenesis of permanent teeth and their association with ectodermal dysplasia syndromes. In this review, we present an overview of the current knowledge regarding genes associated with NSTA and STA, focusing on the distribution and nature of WNT10A and EDA gene mutations. We also explore how these mutations relate to the condition's both forms, including their association with the number of missing permanent teeth.

Indexed as

AnodontiaEctodysplasinsGenetic Association StudiesMutationWnt ProteinsEctodermal DysplasiaGenotypeHumansPhenotypeSyndromeEctodysplasinsEDA protein, humanWNT10A protein, humanWnt Proteins

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.