Evidence map›Paper›PMID 29364747›Full record

ArticleJournal of dental research2018

Rare and Common Variants Conferring Risk of Tooth Agenesis.

L Jonsson, T E Magnusson, A Thordarson, T Jonsson, F Geller, B Feenstra, M Melbye, E A Nohr, S Vucic, B Dhamo and 26 more

Abstract read
In one paragraph

Article in Journal of dental research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
–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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Association between tooth agenesis and cancer: a systematic review.Journal of applied oral science : revista FOB · 2021
    Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Dissecting the Genetic Contribution of Tooth Agenesis.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Main genetic entities associated with tooth agenesis.Clinical oral investigations · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. International journal of molecular sciences · 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

36 authors.

L Jonsson1 deCODE genetics/Amgen, Reykjavik, Iceland.ORCID 0000-0002-3175-103X
T E Magnusson3 Faculty of Odontology, University of Iceland, Reykjavík, Iceland.
A Thordarson3 Faculty of Odontology, University of Iceland, Reykjavík, Iceland.
T Jonsson3 Faculty of Odontology, University of Iceland, Reykjavík, Iceland.
F Geller4 Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
B Feenstra4 Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
M Melbye4 Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
E A Nohr7 Research Unit for Gynaecology and Obstetrics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
S Vucic8 Department of Oral and Maxillofacial Surgery, Special Dental Care and Orthodontics, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0003-3352-3900
B Dhamo8 Department of Oral and Maxillofacial Surgery, Special Dental Care and Orthodontics, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0002-5537-067X
F Rivadeneira9 Generation R Study Group, Erasmus University Medical Centre, Rotterdam, The Netherlands.
E M Ongkosuwito8 Department of Oral and Maxillofacial Surgery, Special Dental Care and Orthodontics, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0001-9250-027X
E B Wolvius8 Department of Oral and Maxillofacial Surgery, Special Dental Care and Orthodontics, Erasmus University Medical Centre, Rotterdam, The Netherlands.
E J Leslie12 Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-5735-1712
M L Marazita12 Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
B J Howe16 Department of Family Dentistry, College of Dentistry, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-6737-9735
L M Moreno Uribe16 Department of Family Dentistry, College of Dentistry, University of Iowa, Iowa City, IA, USA.
I Alonso17 i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
M Santos17 i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
T Pinho17 i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
R Jonsson20 Icelandic Health Insurance, Reykjavík, Iceland.
G Audolfsson21 Department of Plastic Surgery, Landspitali-University Hospital, Reykjavik, Iceland.
L Gudmundsson1 deCODE genetics/Amgen, Reykjavik, Iceland.
M S Nawaz1 deCODE genetics/Amgen, Reykjavik, Iceland.
S Olafsson1 deCODE genetics/Amgen, Reykjavik, Iceland.
O Gustafsson1 deCODE genetics/Amgen, Reykjavik, Iceland.
A Ingason1 deCODE genetics/Amgen, Reykjavik, Iceland.
U Unnsteinsdottir1 deCODE genetics/Amgen, Reykjavik, Iceland.
G Bjornsdottir1 deCODE genetics/Amgen, Reykjavik, Iceland.
G B Walters1 deCODE genetics/Amgen, Reykjavik, Iceland.ORCID 0000-0002-5415-6487
M Zervas1 deCODE genetics/Amgen, Reykjavik, Iceland.
A Oddsson1 deCODE genetics/Amgen, Reykjavik, Iceland.
D F Gudbjartsson1 deCODE genetics/Amgen, Reykjavik, Iceland.
S Steinberg1 deCODE genetics/Amgen, Reykjavik, Iceland.
H Stefansson1 deCODE genetics/Amgen, Reykjavik, Iceland.
K Stefansson1 deCODE genetics/Amgen, Reykjavik, Iceland.

Funding

Extending the Phenotype of Nonsyndromic Orofacial CleftsR01DE016148 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARAZITA, MARY L., WEINBERG, SETH M · 2004 to 2018
$19.7M
Genes for human chronic pain syndromes through whole genome sequencingR01DE022905 · NIDCR · DECODE GENETICS, EHF · PI STEFANSSON, KARI · 2012 to 2016
$2.6M
Genetics of Craniofacial Disorders and Related PhenotypesR00DE025060 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LESLIE-CLARKSON, ELIZABETH JANE · 2017 to 2019
$732k
NIDCR NIH HHS R00 DE025060NIDCR NIH HHS R01 DE016148NIDCR NIH HHS R01 DE022905
6 · The paper itself

Abstract

We present association results from a large genome-wide association study of tooth agenesis (TA) as well as selective TA, including 1,944 subjects with congenitally missing teeth, excluding third molars, and 338,554 controls, all of European ancestry. We also tested the association of previously identified risk variants, for timing of tooth eruption and orofacial clefts, with TA. We report associations between TA and 9 novel risk variants. Five of these variants associate with selective TA, including a variant conferring risk of orofacial clefts. These results contribute to a deeper understanding of the genetic architecture of tooth development and disease. The few variants previously associated with TA were uncovered through candidate gene studies guided by mouse knockouts. Knowing the etiology and clinical features of TA is important for planning oral rehabilitation that often involves an interdisciplinary approach.

Indexed as

AnodontiaFemaleGenome-Wide Association StudyHumansIcelandMalePolymorphism, Single NucleotideRisk Factorsgeneticshypodontiamolecular geneticsodontogenesisoligodontiaorofacial cleft(s)

Identifiers

PMID29364747
PMCPMC5958369

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.