PubMed (OMIM) for id: 80326

Year	Number of Results
1949	1
1956	1
1971	2
1974	1
1976	1
1983	2
1984	1
1986	1
1987	1
1988	1
1992	2
1993	1
1995	3
1996	1
1997	1
2000	1
2001	2
2004	1
2007	2
2009	1
2011	1
2012	1
2013	3
2014	3
2015	1
2017	1
2018	1
2019	1
2024	0

1

Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.

Yu M, Liu Y, Liu H, Wong SW, He H, Zhang X, Wang Y, Han D, Feng H. Yu M, et al. Am J Med Genet A. 2019 Jan;179(1):57-64. doi: 10.1002/ajmg.a.60682. Epub 2018 Dec 20. Am J Med Genet A. 2019. PMID: 30569517

2

WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation.

Xu M, Horrell J, Snitow M, Cui J, Gochnauer H, Syrett CM, Kallish S, Seykora JT, Liu F, Gaillard D, Katz JP, Kaestner KH, Levin B, Mansfield C, Douglas JE, Cowart BJ, Tordoff M, Liu F, Zhu X, Barlow LA, Rubin AI, McGrath JA, Morrisey EE, Chu EY, Millar SE. Xu M, et al. Nat Commun. 2017 Jun 7;8:15397. doi: 10.1038/ncomms15397. Nat Commun. 2017. PMID: 28589954 Free PMC article.

3

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

Yang J, Wang SK, Choi M, Reid BM, Hu Y, Lee YL, Herzog CR, Kim-Berman H, Lee M, Benke PJ, Lloyd KC, Simmer JP, Hu JC. Yang J, et al. Mol Genet Genomic Med. 2015 Jan;3(1):40-58. doi: 10.1002/mgg3.111. Epub 2014 Sep 15. Mol Genet Genomic Med. 2015. PMID: 25629078 Free PMC article.

4

WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N. Arzoo PS, et al. Am J Med Genet A. 2014 Feb;164A(2):353-9. doi: 10.1002/ajmg.a.36243. Epub 2013 Nov 25. Am J Med Genet A. 2014. PMID: 24449199

5

WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.

Kantaputra P, Kaewgahya M, Kantaputra W. Kantaputra P, et al. Am J Med Genet A. 2014 Feb;164A(2):360-3. doi: 10.1002/ajmg.a.36280. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311251

6

Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

Plaisancié J, Bailleul-Forestier I, Gaston V, Vaysse F, Lacombe D, Holder-Espinasse M, Abramowicz M, Coubes C, Plessis G, Faivre L, Demeer B, Vincent-Delorme C, Dollfus H, Sigaudy S, Guillén-Navarro E, Verloes A, Jonveaux P, Martin-Coignard D, Colin E, Bieth E, Calvas P, Chassaing N. Plaisancié J, et al. Am J Med Genet A. 2013 Apr;161A(4):671-8. doi: 10.1002/ajmg.a.35747. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401279

7

Mutations in WNT10A are present in more than half of isolated hypodontia cases.

van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK. van den Boogaard MJ, et al. J Med Genet. 2012 May;49(5):327-31. doi: 10.1136/jmedgenet-2012-100750. J Med Genet. 2012. PMID: 22581971 Free article.

8

WNT10A and isolated hypodontia.

Kantaputra P, Sripathomsawat W. Kantaputra P, et al. Am J Med Genet A. 2011 May;155A(5):1119-22. doi: 10.1002/ajmg.a.33840. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484994

9

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U, Hoffmann M, Ledig S, Sel S, Wieacker P, Röpke A. Bohring A, et al. Am J Hum Genet. 2009 Jul;85(1):97-105. doi: 10.1016/j.ajhg.2009.06.001. Epub 2009 Jun 25. Am J Hum Genet. 2009. PMID: 19559398 Free PMC article.

10

Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E, Belguith H, de Mazancourt P, Megarbane A. Adaimy L, et al. Am J Hum Genet. 2007 Oct;81(4):821-8. doi: 10.1086/520064. Epub 2007 Aug 9. Am J Hum Genet. 2007. PMID: 17847007 Free PMC article.

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