Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
about
A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)A genome-wide association study identifies five loci influencing facial morphology in EuropeansCleft lip and palate: understanding genetic and environmental influencesA genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controlsThe Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics ApproachGenomic expression in non syndromic cleft lip and palate patients: A reviewPalatogenesis and cutaneous repair: A two-headed coinGenetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigeneticsGenetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunitiesNew insights into craniofacial malformationsA mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingInsights into neural crest development and evolution from genomic analysisGenome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociJoint testing of genotypic and gene-environment interaction identified novel association for BMP4 with non-syndromic CL/P in an Asian population using data from an International Cleft Consortium.Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS dataProperties of permutation-based gene tests and controlling type 1 error using a summary statistic based gene testImputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern ChinaExploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effectsOn the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.Improving human forensics through advances in genetics, genomics and molecular biology.PVRL1 as a candidate gene for nonsyndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in southern Han Chinese patients.BMP4 was associated with NSCL/P in an Asian population.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.X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia.SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.Age of onset and effect size in genome-wide association studiesFAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish.Polymorphisms in FGF12, VCL, CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palateSusceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate.TGFA and IRF6 contribute to the risk of nonsyndromic cleft lip with or without cleft palate in northeast ChinaDetecting genetic association of common human facial morphological variation using high density 3D image registrationEvidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.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.Genetic determination of human facial morphology: links between cleft-lips and normal variation.Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.Epigenomics of human embryonic stem cells and induced pluripotent stem cells: insights into pluripotency and implications for disease.
P2860
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P2860
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genome-wide association study ...... with or without cleft palate.
@ast
Genome-wide association study ...... with or without cleft palate.
@en
Genome-wide association study ...... with or without cleft palate.
@nl
type
label
Genome-wide association study ...... with or without cleft palate.
@ast
Genome-wide association study ...... with or without cleft palate.
@en
Genome-wide association study ...... with or without cleft palate.
@nl
prefLabel
Genome-wide association study ...... with or without cleft palate.
@ast
Genome-wide association study ...... with or without cleft palate.
@en
Genome-wide association study ...... with or without cleft palate.
@nl
P2093
P50
P356
P1433
P1476
Genome-wide association study ...... with or without cleft palate.
@en
P2093
Alexander Hemprich
Bert Braumann
Bettina Blaumeiser
Carlotta Baluardo
Carola Lauster
Elisabeth Mangold
Franz-Josef Kramer
Gül Schmidt
Hans-Erich Wichmann
P2888
P356
10.1038/NG.506
P407
P50
P577
2009-12-20T00:00:00Z