Role of WNT10A in failure of tooth development in humans and zebrafish

Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis

(2017) N. Dinckan et al.   JOURNAL OF DENTAL RESEARCH

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

(2017) Mingang Xu et al.   Nature Communications

Mutations in WNT10B Are Identified in Individuals with Oligodontia

(2016) Ping Yu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

(2016) Xiaoming Liu et al.   HUMAN MUTATION

Robust classification of protein variation using structural modelling and large-scale data integration

(2016) Evan H. Baugh et al.   NUCLEIC ACIDS RESEARCH

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

The Gene Network Underlying Hypodontia

(2015) W. Yin et al.   JOURNAL OF DENTAL RESEARCH

Is there a link between ovarian cancer and tooth agenesis?

(2014) John Bonds et al.   European Journal of Medical Genetics

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

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

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

WNT10A variants are associated with non-syndromic tooth agenesis in the general population

(2013) Shujuan Song et al.   HUMAN GENETICS

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

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

WNT10A and isolated hypodontia

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

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

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

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS 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

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Wnt/beta-catenin signaling plays an essential role in activation of odontogenic mesenchyme during early tooth development

(2009) Jianquan Chen et al.   DEVELOPMENTAL BIOLOGY

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis

(2008) Dong Han et al.   European Journal of Medical Genetics

Analyzing real-time PCR data by the comparative CT method

(2008) Thomas D Schmittgen et al.   Nature Protocols