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
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from ScandinaviaCleft lip and palate: understanding genetic and environmental influencesTesting reported associations of genetic risk factors for oral clefts in a large Irish study populationFOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateGenomic expression in non syndromic cleft lip and palate patients: A reviewGenetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunitiesJoint 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.Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populationsWhole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral cleftsApproaches for evaluating rare polymorphisms in genetic association studiesEvidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate.BMP4 was associated with NSCL/P in an Asian population.CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate.Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palateIdentification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesThe functional EGF+61 polymorphism and nonsyndromic oral clefts susceptibility in a Brazilian population.ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian populationThe FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese populationCandidate pathway based analysis for cleft lip with or without cleft palate.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 cleftsClinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian populationGWAS reveals new recessive loci associated with non-syndromic facial cleftingSequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.Disruption of the murine Ap2β1 gene causes nonsyndromic cleft palate.Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio studyHistone acetylation is involved in TCDD‑induced cleft palate formation in fetal mice.The evolution of human genetic studies of cleft lip and cleft palate.Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population.Genetics of cleft lip and cleft palate.Rehabilitative treatment of cleft lip and palate: experience of the Hospital for Rehabilitation of Craniofacial Anomalies/USP (HRAC/USP)--Part 1: overall aspectsDiazepam effects on non-syndromic cleft lip with or without palate: epidemiological studies, clinical findings, genes and extracellular matrix.The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan AfricaNonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen.Descriptive analysis of high birth prevalence rate geographical clusters of congenital anomalies in South America.Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population.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.
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P2860
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
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 11 June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genome scan, fine-mapping, and ...... inkage and association results
@en
Genome scan, fine-mapping, and ...... nkage and association results.
@nl
type
label
Genome scan, fine-mapping, and ...... inkage and association results
@en
Genome scan, fine-mapping, and ...... nkage and association results.
@nl
prefLabel
Genome scan, fine-mapping, and ...... inkage and association results
@en
Genome scan, fine-mapping, and ...... nkage and association results.
@nl
P2093
P2860
P356
P1433
P1476
Genome scan, fine-mapping, and ...... inkage and association results
@en
P2093
Alexandre R Vieira
Andrew C Lidral
Astanand Jugessur
Bridget Riley
Brion S Maher
Consuelo Valencia-Ramirez
Elizabeth Pugh
Jeffrey C Murray
Kim Doheny
L Leigh Field
P2860
P304
P356
10.1159/000224636
P577
2009-06-11T00:00:00Z