Evidence map›Paper›PMID 34036831›Full record

ArticleJournal of dental research2022

Recessive Mutations in

Y J Kim, Y Lee, Y Kasimoglu, F Seymen, J P Simmer, J C-C Hu, E-S Cho, J-W Kim

Open access · greenAbstract read
In one paragraph

Article in Journal of dental research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. ACP4 Variants in Hypoplastic Amelogenesis Imperfecta.Calcified tissue international · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. NovelJournal of personalized medicine · 2024
    Article
  7. RecessiveJournal of personalized medicine · 2023
    Article
  8. NovelJournal of personalized medicine · 2023
    Article
  9. Enamel defects in Acp4Scientific reports · 2022
    Article
  10. Translated MutantJournal of personalized medicine · 2022
    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

8 authors at 4 institutions in 3 countries.

Y J KimDepartment of Molecular Genetics and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Republic of Korea.
Y LeeDepartment of Pediatric Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Republic of Korea.
Y KasimogluDepartment of Pedodontics, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.
F SeymenDepartment of Pedodontics, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.
J P SimmerDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-7192-6105
J C-C HuDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.
E-S ChoCluster for Craniofacial Development and Regeneration Research, Institute of Oral Biosciences, Jeonbuk National University School of Dentistry, Jeonju, Republic of Korea.
J-W KimDepartment of Molecular Genetics and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-9399-2197
Seoul National University · KRIstanbul University · TRUniversity of Michigan · USJeonbuk National University · KR

Funding

Proteomics and Genetics of Enamel and DentinR01DE015846 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HU, JAN CHING CHUN · 2004 to 2019
$5.7M
Genetic Mechanisms of Amelogenesis ImperfectaR56DE015846 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HU, JAN CHING CHUN · 2021 to 2021
$402k
NIDCR NIH HHS R01 DE015846NIDCR NIH HHS R56 DE015846
6 · The paper itself

Abstract

Amelogenesis imperfecta (AI) is an innate disorder that affects the formation and mineralization of the tooth enamel. When diagnosed with AI, one's teeth can be hypoplastic (thin enamel), hypomature (normal enamel thickness but discolored and softer than normal enamel), hypocalcified (normal enamel thickness but extremely weak), or mixed conditions of the above. Numerous studies have revealed the genes that are involved in causing AI. Recently,

Indexed as

Amelogenesis ImperfectaToothAcid PhosphataseDental EnamelHumansMutationPedigreeAcid PhosphataseACP4 protein, humanacid phosphatase 4compound heterozygous mutationde novo mutationdimerizationenamelhereditary

Identifiers

PMID34036831
PMCPMC8721729
OpenAlexW3165713111

What OpenQuestion holds

Textmetadata
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.