Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway
about
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeMissense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6Genomic expression in non syndromic cleft lip and palate patients: A reviewGenetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Addressing the challenges of cleft lip and palate research in IndiaAssociation between IRF6 SNPs and oral clefts in West ChinaEvidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate.Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palateEthnic heterogeneity of IRF6 AP-2a binding site promoter SNP association with nonsyndromic cleft lip and palateA combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.Human atopic dermatitis complicated by eczema herpeticum is associated with abnormalities in IFN-γ response.TGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast ChinaKey susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data.Risk prediction models for oral clefts allowing for phenotypic heterogeneity.Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia.Genetics of nonsyndromic orofacial cleftsIdentification of microdeletions in candidate genes for cleft lip and/or palate.The evolution of human genetic studies of cleft lip and cleft palate.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 resultsGenetics of cleft lip and cleft palate.Diazepam effects on non-syndromic cleft lip with or without palate: epidemiological studies, clinical findings, genes and extracellular matrix.Genomic approaches for studying craniofacial disorders.Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil.Association between IRF6 and 8q24 polymorphisms and nonsyndromic cleft lip with or without cleft palate: Systematic review and meta-analysis.Genetic analysis of IRF6, a gene involved in craniofacial midline formation, in relation to pituitary and facial morphology of patients with idiopathic growth hormone deficiency.IRF6 polymorphisms in Mexican patients with non-syndromic cleft lip.Craniofacial abnormalities result from knock down of nonsyndromic clefting gene, crispld2, in zebrafishIRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population.Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the southeast Iranian population.Replication of two novel susceptibility loci for non-syndromic orofacial clefts in a Chinese population.A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians.Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot.IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
P2860
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P2860
Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Genetic variants in IRF6 and t ...... udy of facial clefts in Norway
@en
Genetic variants in IRF6 and t ...... dy of facial clefts in Norway.
@nl
type
label
Genetic variants in IRF6 and t ...... udy of facial clefts in Norway
@en
Genetic variants in IRF6 and t ...... dy of facial clefts in Norway.
@nl
prefLabel
Genetic variants in IRF6 and t ...... udy of facial clefts in Norway
@en
Genetic variants in IRF6 and t ...... dy of facial clefts in Norway.
@nl
P2093
P2860
P356
P1433
P1476
Genetic variants in IRF6 and t ...... udy of facial clefts in Norway
@en
P2093
Astanand Jugessur
Fedik Rahimov
Jeffrey C Murray
Rolv T Lie
Roy M Nilsen
Truc Trung Nguyen
P2860
P304
P356
10.1002/GEPI.20314
P577
2008-07-01T00:00:00Z