Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series

PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China

(2017) Jing WANG et al.   Journal of Applied Oral Science

Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis

(2016) Marwa Haddaji Mastouri et al.   ARCHIVES OF ORAL BIOLOGY

Functional analysis of a novel missense mutation inAXIN2associated with non-syndromic tooth agenesis

(2016) Haitang Yue et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

DNA methylation is critical for tooth agenesis: implications for sporadic non-syndromic anodontia and hypodontia

(2016) Jing Wang et al.   Scientific Reports

The Gene Network Underlying Hypodontia

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

ClinVar: public archive of interpretations of clinically relevant variants

(2015) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia

(2014) Singwai Wong et al.   ARCHIVES OF ORAL BIOLOGY

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

Intra-epithelial Requirement of Canonical Wnt Signaling for Tooth Morphogenesis

(2013) XiaoJing Zhu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Polymorphism in the MSX1 gene in a family with upper lateral incisor agenesis

(2012) B.R. Boeira Junior et al.   ARCHIVES OF ORAL BIOLOGY

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population

(2012) Haochen Liu et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

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

Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family

(2011) Jing Wang et al.   ARCHIVES OF ORAL BIOLOGY

Genetic Studies in the Nigerian Population Implicate an MSX1 Mutation in Complex Oral Facial Clefting Disorders

(2011) A. Butali et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis

(2010) Vanessa Rodrigues Paixão-Côrtes et al.   ARCHIVES OF ORAL BIOLOGY

Mutations in the PAX9 gene in sporadic oligodontia

(2010) E Pawlowska et al.   Orthodontics & Craniofacial 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

Tooth Agenesis: from Molecular Genetics to Molecular Dentistry

(2009) E. Matalova et al.   JOURNAL OF DENTAL RESEARCH

Genetic basis of tooth agenesis

(2009) Pekka Nieminen   JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Mutations in the Human Homeobox MSX1 Gene in the Congenital Lack of Permanent Teeth

(2009) Elzbieta Pawlowska et al.   TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis

(2008) N. Callahan et al.   ARCHIVES OF ORAL BIOLOGY

PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case–control study in southeast China

(2008) Yongchu Pan et al.   EUROPEAN JOURNAL OF ORAL SCIENCES