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For: Krøigård AB, Clemmensen O, Gjørup H, Hertz JM, Bygum A. Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation. BMC Dermatol 2016;16:3. [PMID: 26964878 DOI: 10.1186/s12895-016-0040-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
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1 Higashino T, Lee JYW, Mcgrath JA. Advances in the genetic understanding of hypohidrotic ectodermal dysplasia. Expert Opinion on Orphan Drugs 2017;5:967-75. [DOI: 10.1080/21678707.2017.1405806] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
2 Ruiz-Heiland G, Lenz S, Bock N, Ruf S. Prevalence of WNT10A gene mutations in non-syndromic oligodontia. Clin Oral Investig 2019;23:3103-13. [PMID: 30426266 DOI: 10.1007/s00784-018-2731-4] [Cited by in Crossref: 4] [Article Influence: 1.0] [Reference Citation Analysis]
3 Said NM, Yassin F, Elkreem EA. Wnt10a missense gene polymorphism association with obesity risk: List of literature and a case-control study with Roc analysis for serum β-catenin level in Egypt. Gene Reports 2022. [DOI: 10.1016/j.genrep.2022.101496] [Reference Citation Analysis]
4 Yu M, Liu Y, Liu H, Wong S, He H, Zhang X, Wang Y, Han D, Feng H. Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia. Am J Med Genet 2019;179:57-64. [DOI: 10.1002/ajmg.a.60682] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
5 Sinada N, Wang CI. Fixed prosthodontic rehabilitation for an adult with ectodermal dysplasia using a completely digital workflow. J Prosthet Dent 2021:S0022-3913(21)00417-0. [PMID: 34696906 DOI: 10.1016/j.prosdent.2021.07.022] [Reference Citation Analysis]