Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency

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

(2015) Maarten P.G. Massink et al.   AMERICAN JOURNAL OF HUMAN GENETICS

WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma

(2015) Apple Long et al.   CARCINOGENESIS

Common polymorphisms in WNT10A affect tooth morphology as well as hair shape

(2015) Ryosuke Kimura et al.   HUMAN MOLECULAR GENETICS

Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations

(2014) P. Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Orodental manifestations in ectodermal dysplasia-A review

(2014) Birgitta Bergendal   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The WNT10A gene in ectodermal dysplasias and selective tooth agenesis

(2014) Gabriele Mues et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

EDAR-induced hypohidrotic ectodermal dysplasia: a clinical study on signs and symptoms in individuals with a heterozygous c.1072C > T mutation

(2014) Catarina Falk Kieri et al.   BMC Medical Genetics

Clinical features andWNT10Amutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome

(2014) C. Tziotzios et al.   BRITISH JOURNAL OF DERMATOLOGY

Variability in dentofacial phenotypes in four families with WNT10A mutations

(2014) Christian P Vink et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Taurodontism, variations in tooth number, and misshapened crowns inWnt10anull mice and human kindreds

(2014) Jie Yang et al.   Molecular Genetics & Genomic Medicine

Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

(2013) Julie Plaisancié et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations

(2013) Pakeeza Shaiq Arzoo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Candidate Gene Analysis of Tooth Agenesis Identifies Novel Mutations in Six Genes and Suggests Significant Role for WNT and EDA Signaling and Allele Combinations

(2013) Sirpa Arte et al.   PLoS One

Wnt/β-Catenin Signaling and Disease

(2012) Hans Clevers et al.   CELL

Tooth shape formation and tooth renewal: evolving with the same signals

(2012) J. Jernvall et al.   DEVELOPMENT

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

(2012) Marie-José van den Boogaard et al.   JOURNAL OF MEDICAL GENETICS

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

(2010) Céline Cluzeau et al.   HUMAN MUTATION

Wnt/β-catenin Signaling in Oral Tissue Development and Disease

(2010) F. Liu et al.   JOURNAL OF DENTAL RESEARCH

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

(2009) Axel Bohring et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Ectodermal dysplasias: Clinical and molecular review

(2009) Átila F. Visinoni et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

(2009) Sadia Nawaz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS