Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia-Reference-Cited by-同舟云学术

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia

Published:2015-10 Issue:4 Volume:97 Page:621-626
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Massink Maarten P.G.,Créton Marijn A.,Spanevello Francesca,Fennis Willem M.M.,Cune Marco S.,Savelberg Sanne M.C.,Nijman Isaäc J.,Maurice Madelon M.,van den Boogaard Marie-José H.,van Haaften Gijs

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

1. A meta-analysis of the prevalence of dental agenesis of permanent teeth;Polder;Community Dent. Oral Epidemiol.,2004

2. Genetic basis of tooth agenesis;Nieminen;J. Exp. Zoolog. B Mol. Dev. Evol.,2009

3. Patterns of missing teeth in a population of oligodontia patients;Créton;Int. J. Prosthodont.,2007

4. Dentofacial characteristics of patients with hypodontia;Créton;Clin. Oral Investig.,2010

5. Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental development;Brook;Arch. Oral Biol.,2009

Cited by 92 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia;BMC Oral Health;2024-01-27

2. Whole genome sequencing in families with oligodontia;Oral Diseases;2023-12-09

3. FGFR1 variants contributed to families with tooth agenesis;Human Genomics;2023-10-13

4. PAX9 mutations and genetic synergism in familial tooth agenesis;Annals of the New York Academy of Sciences;2023-04-02

5. Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontia;Frontiers in Genetics;2023-03-28