Evidence map›Paper›PMID 35707781›Full record

ReviewGlobal medical genetics2022

The Human Genetics of Dental Anomalies.

Mahamad Irfanulla Khan, Nadeem Ahmed, Praveen Kumar Neela, Nayeem Unnisa

Abstract readReview
In one paragraph

Review in Global medical genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. 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. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Main genetic entities associated with tooth agenesis.Clinical oral investigations · 2024
    Review
  12. Association between molar incisor hypomineralisation and tooth agenesis: a cross-sectional study in Brazilian children and adolescents.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Tooth number abnormality: from bench to bedside.International journal of oral science · 2023
    Review
  17. 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

4 authors.

Mahamad Irfanulla KhanDepartment of Orthodontics & Dentofacial Orthopedics, The Oxford Dental College, Bangalore, Karnataka, India.ORCID 0000-0003-0164-8143
Nadeem AhmedGeneral Dental Practitioner, Max Dental Specialties, Bangalore, Karnataka, India.
Praveen Kumar NeelaDepartment of Orthodontics & Dentofacial Orthopedics, Kamineni Institute of Dental Sciences, Narketpally, Andhra Pradesh, India.
Nayeem UnnisaGeneral Dental Practitioner, The Dental Clinic, Bangalore, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of tooth is a highly complex procedure and mastered by specific genetic programs. Genetic alterations, environmental factors, and developmental timing can disturb the execution of these programs, and result in various dental anomalies like hypodontia/oligodontia, and supernumerary teeth, which are commonly seen in our clinical practice. Advances in molecular research enabled the identification of various genes involved in the pathogenesis of dental anomalies. In the near future, it will help provide a more accurate diagnosis and biological-based treatment for these anomalies. In this article, we present the molecular phenomenon of tooth development and the genetics of various dental anomalies.

Indexed as

dental anomaliesgenesgeneticsmutationstooth development

Identifiers

PMID35707781
PMCPMC9192175

What OpenQuestion holds

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LicenceCC BY
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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.