Evidence map›Paper›PMID 28473773›Full record

ArticleFrontiers in physiology2017

Analyses of

Youn Jung Kim, Jenny Kang, Figen Seymen, Mine Koruyucu, Koray Gencay, Teo Jeon Shin, Hong-Keun Hyun, Zang Hee Lee, Jan C-C Hu, James P Simmer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Integrative multi-omics and bioinformatic analysis ofThe Japanese dental science review · 2026
    Review
  2. NovelGenes · 2026
    Article
  3. NovelJournal of dental sciences · 2026
    Article
  4. Review
  5. Article
  6. Importance of Metalloproteinase 8 (MMP-8) in the Diagnosis of Periodontitis.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Article
  9. Frontiers in physiology · 2023
    Article
  10. Article
  11. Dental malformations associated with biallelic MMP20 mutations.Molecular genetics & genomic medicine · 2020
    Article
  12. Article
  13. Article
  14. 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

11 authors at 3 institutions in 3 countries.

Youn Jung KimDepartment of Molecular Genetics and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Jenny KangDepartment of Pediatric Dentistry and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Figen SeymenFaculty of Dentistry, Department of Pedodontics, Istanbul UniversityIstanbul, Turkey.
Mine KoruyucuFaculty of Dentistry, Department of Pedodontics, Istanbul UniversityIstanbul, Turkey.
Koray GencayFaculty of Dentistry, Department of Pedodontics, Istanbul UniversityIstanbul, Turkey.
Teo Jeon ShinDepartment of Pediatric Dentistry and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Hong-Keun HyunDepartment of Pediatric Dentistry and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Zang Hee LeeDepartment of Cell and Developmental Biology and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Jan C-C HuDepartment of Biologic and Materials Sciences, University of Michigan School of DentistryAnn Arbor, MI, USA.
James P SimmerDepartment of Biologic and Materials Sciences, University of Michigan School of DentistryAnn Arbor, MI, USA.
Jung-Wook KimDepartment of Molecular Genetics and Dental Research Institute, School of Dentistry, Seoul National UniversitySeoul, Korea.
Seoul National University Dental Hospital · KRIstanbul University · TRUniversity of Michigan · US

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
NIDCR NIH HHS R01 DE015846
6 · The paper itself

Abstract

Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or qualitatively. The aim of this study was to identify the genetic etiologies of two families presenting with hypomaturation amelogenesis imperfecta. DNA was isolated from peripheral blood samples obtained from participating family members. Whole exome sequencing was performed using DNA samples from the two probands. Sequencing data was aligned to the NCBI human reference genome (NCBI build 37.2, hg19) and sequence variations were annotated with the dbSNP build 138. Mutations in

Indexed as

amelogenesis imperfectaenamelenamelysinhypomaturationmatrixproteinase

Identifiers

PMID28473773
PMCPMC5397402
OpenAlexW2608670853

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.