Evidence map›Paper›PMID 37228816›Full record

ArticleFrontiers in physiology2023

Agnes Bloch-Zupan, Tristan Rey, Alexandra Jimenez-Armijo, Marzena Kawczynski, Naji Kharouf, O-Rare consortium, Muriel de La Dure-Molla, Emmanuelle Noirrit, Magali Hernandez, Clara Joseph-Beaudin and 16 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
13.7field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Integrative multi-omics and bioinformatic analysis ofThe Japanese dental science review · 2026
    Review
  4. Article
  5. Evaluating a condition-specific PROM for amelogenesis imperfecta in children and young people: insights from patients and clinicians.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. ACP4 Variants in Hypoplastic Amelogenesis Imperfecta.Calcified tissue international · 2026
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. NovelJournal of dental sciences · 2026
    Article
  17. Article
  18. Review
  19. Article
  20. Genes · 2025
    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

26 authors at 16 institutions in 6 countries.

Agnes Bloch-ZupanUniversité de Strasbourg, Faculté de Chirurgie Dentaire, Strasbourg, France.
Tristan ReyUniversité de Strasbourg, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), IN-SERM U1258, CNRS- UMR7104, Illkirch, France.
Alexandra Jimenez-ArmijoUniversité de Strasbourg, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), IN-SERM U1258, CNRS- UMR7104, Illkirch, France.
Marzena KawczynskiHôpitaux Universitaires de Strasbourg (HUS), Pôle de Médecine et Chirurgie Bucco-dentaires, Hôpital Civil, Centre de référence des maladies rares orales et dentaires, O-Rares, Filiére Santé Maladies rares TETE COU, European Reference Network ERN CRANIO, Strasbourg, France.
Naji KharoufUniversité de Strasbourg, Laboratoire de Biomatériaux et Bioingénierie, Inserm UMR_S 1121, Strasbourg, France.
O-Rare consortium
Muriel de La Dure-MollaRothschild Hospital, Public Assistance-Paris Hospitals (AP-HP), Reference Center for Rare Oral and Den-tal Diseases (O-Rares), Paris, France.
Emmanuelle NoirritCentre Hospitalier Universitaire (CHU) Rangueil, Toulouse, Competence Center for Rare Oral and Den-tal Diseases, Toulouse, France.
Magali HernandezCentre Hospitalier Régional Universitaire de Nancy, Université de Lorraine, Competence Center for Rare Oral and Dental Diseases, Nancy, France.
Clara Joseph-BeaudinCentre Hospitalier Universitaire de Nice, Competence Center for Rare Oral and Dental Diseases, Nice, France.
Serena LopezCentre Hospitalier Universitaire de Nantes, Competence Center for Rare Oral and Dental Diseases, Nantes, France.
Corinne TardieuAPHM, Hôpitaux Universitaires de Marseille, Hôpital Timone, Competence Center for Rare Oral and Dental Diseases, Marseille, France.
Béatrice Thivichon-PrinceCentre Hospitalier Universitaire de Lyon, Competence Center for Rare Oral and Dental Diseases, Lyon, France.
ERN Cranio Consortium
Tatjana DostalovaDepartment of Stomatology (TD) and Department of Biology and Medical Genetics (MM) Charles University 2nd Faculty of Medicine and Motol University Hospital, Prague, Czechia.
Milan MacekDepartment of Stomatology (TD) and Department of Biology and Medical Genetics (MM) Charles University 2nd Faculty of Medicine and Motol University Hospital, Prague, Czechia.
International Consortium
Mustapha El AlloussiFaculty of Dentistry, International University of Rabat, CReSS Centre de recherche en Sciences de la Santé, Rabat, Morocco.
Leila QebiboUnité de génétique médicale et d'oncogénétique, CHU Hassan II, Fes, Morocco.
Supawich MorkmuedFaculty of Dentistry, Khon Kaen University, Khon Kaen, Thailand.
Patimaporn PungchanchaikulFaculty of Dentistry, Khon Kaen University, Khon Kaen, Thailand.
Blanca Urzúa OrellanaInstituto de Investigación en Ciencias Odontológicas, Facultad de Odontología, Universidad de Chile, Santiago, Chile.
Marie-Cécile ManièreUniversité de Strasbourg, Faculté de Chirurgie Dentaire, Strasbourg, France.
Bénédicte GérardHôpitaux Universitaires de Strasbourg, Laboratoires de diagnostic génétique, Institut de Génétique Médicale d'Alsace, Strasbourg, France.
Isaac Maximiliano BuguenoUniversité de Strasbourg, Faculté de Chirurgie Dentaire, Strasbourg, France.
Virginie Laugel-HaushalterUniversité de Strasbourg, Faculté de Chirurgie Dentaire, Strasbourg, France.
Centre National de la Recherche Scientifique · FRCharles University · CZKhon Kaen University · THSorbonne Université · FRAix-Marseille Université · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Nice · FRHôpitaux Universitaires de Strasbourg · FRInserm · FRInstitut de génétique et de biologie moléculaire et cellulaire · FRMohammed V University · MARegenerative NanoMedicine · FRUniversité Claude Bernard Lyon 1 · FRUniversité Toulouse III - Paul Sabatier · FRUniversity of Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel phenotypes can be described as hypoplastic, hypomineralized or hypomature and serve as a basis, together with the mode of inheritance, to Witkop's classification (Witkop, J Oral Pathol, 1988, 17, 547-553). AI can be described in isolation or associated with others symptoms in syndromes. Its occurrence was estimated to range from 1/700 to 1/14,000. More than 70 genes have currently been identified as causative.

Indexed as

amelogenesis imperfectaenamelgeneticsnext-generation sequencingNGSrare diseases

Identifiers

PMID37228816
PMCPMC10205041
OpenAlexW4378348417

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.