Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-12-24
DOI
10.1002/ajmg.a.61002
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome
- (2018) Roser Urreizti et al. Scientific Reports
- Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate
- (2017) Elizabeth J. Leslie et al. HUMAN GENETICS
- Exploring Subclinical Phenotypic Features in Twin Pairs Discordant for Cleft Lip and Palate
- (2017) Elizabeth J. Leslie et al. CLEFT PALATE-CRANIOFACIAL JOURNAL
- A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
- (2016) Elizabeth J. Leslie et al. AMERICAN JOURNAL OF HUMAN GENETICS
- RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data: Table 1.
- (2016) Xiaowei Zhan et al. BIOINFORMATICS
- Expression of forkhead box transcription factor genes Foxp1 and Foxp2 during jaw development
- (2016) Jeffry M. Cesario et al. GENE EXPRESSION PATTERNS
- Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci
- (2015) Elizabeth J. Leslie et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Enhancer Divergence and cis-Regulatory Evolution in the Human and Chimp Neural Crest
- (2015) Sara L. Prescott et al. CELL
- Lhx6andLhx8promote palate development through negative regulation of a cell cycle inhibitor gene,p57Kip2
- (2015) Jeffry M. Cesario et al. HUMAN MOLECULAR GENETICS
- A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1
- (2015) Andrew C. Lidral et al. HUMAN MOLECULAR GENETICS
- Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate
- (2015) Yimin Sun et al. Nature Communications
- Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate
- (2015) Zena T. Wolf et al. PLoS Genetics
- Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants withinGremlin-1, a component of the bone morphogenetic protein 4 pathway
- (2014) Taofik Al Chawa et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts
- (2014) A. Bureau et al. GENETICS
- FOXP1mutations cause intellectual disability and a recognizable phenotype
- (2013) Anna K. Le Fevre et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetics of cleft lip and cleft palate
- (2013) Elizabeth J. Leslie et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers
- (2013) C. Attanasio et al. SCIENCE
- The Evolution of Human Genetic Studies of Cleft Lip and Cleft Palate
- (2012) Mary L. Marazita Annual Review of Genomics and Human Genetics
- Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22
- (2012) Elizabeth J. Leslie et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate
- (2012) EJ Leslie et al. CLINICAL GENETICS
- Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
- (2012) Kerstin U Ludwig et al. NATURE GENETICS
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3
- (2010) John W. Pierpont et al. CLINICAL GENETICS
- A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
- (2010) Terri H Beaty et al. NATURE GENETICS
- Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip
- (2009) Satoshi Suzuki et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results
- (2009) Mary L. Marazita et al. HUMAN HEREDITY
- FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
- (2009) Lina M. Moreno et al. HUMAN MOLECULAR GENETICS
- A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24
- (2009) Struan F.A. Grant et al. JOURNAL OF PEDIATRICS
- Genomic views of distant-acting enhancers
- (2009) Axel Visel et al. NATURE
- Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
- (2009) Elisabeth Mangold et al. NATURE GENETICS
- Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
- (2009) Stefanie Birnbaum et al. NATURE GENETICS
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
- (2009) Bryan N. Howie et al. PLoS Genetics
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
- (2008) Fedik Rahimov et al. NATURE GENETICS
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started