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Cleft lip and palate: understanding genetic and environmental influences
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470015902.a0020915openalex-snapshot
Craniofacial Defects and Cleft Lip and Palate
inferredcites →https://doi.org/10.1002/ajmg.a.30806openalex-snapshot
Hair whorls and handedness: Informative phenotypic markers in nonsyndromic cleft lip with or without cleft palate (NS CL/P) cases and their unaffected relatives
inferredcites →https://doi.org/10.1002/ajmg.a.30887openalex-snapshot
Variation in IRF6 contributes to nonsyndromic cleft lip and palate
inferredcites →https://doi.org/10.1002/ajmg.a.31367openalex-snapshot
PVRL1 variants contribute to non‐syndromic cleft lip and palate in multiple populations
inferredcites →https://doi.org/10.1002/ajmg.a.31760openalex-snapshot
Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate
inferredcites →https://doi.org/10.1002/ajmg.a.31965openalex-snapshot
Sequence evaluation of FGF and FGFR gene conserved non‐coding elements in non‐syndromic cleft lip and palate cases
inferredcites →https://doi.org/10.1002/ajmg.a.32177openalex-snapshot
Three‐dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility
inferredcites →https://doi.org/10.1002/ajmg.a.32291openalex-snapshot
Rethinking isolated cleft palate: Evidence of occult lip defects in a subset of cases
inferredcites →https://doi.org/10.1002/ajmg.a.32854openalex-snapshot
Orofacial clefts in the National Birth Defects Prevention Study, 1997–2004
inferredcites →https://doi.org/10.1002/ajmg.a.33089openalex-snapshot
Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate
inferredcites →https://doi.org/10.1002/ajmg.a.33479openalex-snapshot
Folic acid flour fortification: Impact on the frequencies of 52 congenital anomaly types in three South American countries
inferredcites →https://doi.org/10.1002/ajmg.a.33695openalex-snapshot
Revisiting the recurrence risk of nonsyndromic cleft lip with or without cleft palate
inferredcites →https://doi.org/10.1002/bdra.20106openalex-snapshot
Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice
inferredcites →https://doi.org/10.1002/bdra.20302openalex-snapshot
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
inferredcites →https://doi.org/10.1002/bdra.20319openalex-snapshot
Reduction in orofacial clefts following folic acid fortification of the U.S. grain supply
inferredcites →https://doi.org/10.1002/bdra.20491openalex-snapshot
Folate‐related gene polymorphisms as risk factors for cleft lip and cleft palate
inferredcites →https://doi.org/10.1002/bdra.20516openalex-snapshot
Plasma zinc concentrations of mothers and the risk of oral clefts in their children in Utah
inferredcites →https://doi.org/10.1002/bdra.20571openalex-snapshot
Identification of microdeletions in candidate genes for cleft lip and/or palate
inferredcites →https://doi.org/10.1002/bdra.20639openalex-snapshot
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population
inferredcites →https://doi.org/10.1002/bdra.20646openalex-snapshot
Maternal fever during early pregnancy and the risk of oral clefts
inferredcites →https://doi.org/10.1002/bdra.20687openalex-snapshot
Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population
inferredcites →https://doi.org/10.1002/bdrb.20252openalex-snapshot
The etiology of cleft palate: a 50‐year search for mechanistic and molecular understanding
inferredcites →https://doi.org/10.1002/bdrc.20117openalex-snapshot
Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects
inferredcites →https://doi.org/10.1002/dvdy.20646openalex-snapshot
Development of the upper lip: Morphogenetic and molecular mechanisms
inferredcites →https://doi.org/10.1002/dvdy.20723openalex-snapshot
Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice
inferredcites →https://doi.org/10.1002/gepi.1039openalex-snapshot
Testing candidate genes for non‐syndromic oral clefts using a case‐parent trio design
inferredcites →https://doi.org/10.1002/gepi.20376openalex-snapshot
Oral facial clefts and gene polymorphisms in metabolism of folate/one‐carbon and vitamin A: a pathway‐wide association study
inferredcites →https://doi.org/10.1002/gepi.20492openalex-snapshot
The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions
inferredcites →https://doi.org/10.1002/humu.21328openalex-snapshot
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations
inferredcites →https://doi.org/10.1002/sim.3255openalex-snapshot
‘Mendelian randomization’ equals instrumental variable analysis with genetic instruments
inferredcites →https://doi.org/10.1007/bf01507412openalex-snapshot
Inheritance of harelip and cleft palate
inferredcites →https://doi.org/10.1007/s00439-010-0863-yopenalex-snapshot
Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate
inferredcites →https://doi.org/10.1016/0092-8674(94)90041-8openalex-snapshot
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
inferredcites →https://doi.org/10.1016/0092-8674(94)90281-xopenalex-snapshot
The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
inferredcites →https://doi.org/10.1016/j.ajhg.2008.03.005openalex-snapshot
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome
inferredcites →https://doi.org/10.1016/j.ajhg.2009.02.002openalex-snapshot
Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip
inferredcites →https://doi.org/10.1016/j.devcel.2005.05.016openalex-snapshot
Wnt9b Plays a Central Role in the Regulation of Mesenchymal to Epithelial Transitions Underlying Organogenesis of the Mammalian Urogenital System
inferredcites →https://doi.org/10.1016/j.ijom.2009.10.010openalex-snapshot
Analysis of interactions between genetic variants of BMP4 and environmental factors with nonsyndromic cleft lip with or without cleft palate susceptibility
inferredcites →https://doi.org/10.1016/j.jchromb.2006.03.028openalex-snapshot
FOXE1 gene mutation screening by multiplex PCR/DHPLC in CHARGE syndrome and syndromic and non-syndromic cleft palate
inferredcites →https://doi.org/10.1016/j.jpeds.2009.06.020openalex-snapshot
A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24
inferredcites →https://doi.org/10.1016/j.ydbio.2006.07.042openalex-snapshot
Molecular control of secondary palate development
inferredcites →https://doi.org/10.1016/j.ydbio.2010.12.028openalex-snapshot
Bmpr1a signaling plays critical roles in palatal shelf growth and palatal bone formation
inferredcites →https://doi.org/10.1016/s0092-8674(00)81268-4openalex-snapshot
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
inferredcites →https://doi.org/10.1016/s0092-8674(00)81646-3openalex-snapshot
Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome
inferredcites →https://doi.org/10.1034/j.1399-0004.2002.610402.xopenalex-snapshot
Gene/environment causes of cleft lip and/or palate
inferredcites →https://doi.org/10.1038/1294openalex-snapshot
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
inferredcites →https://doi.org/10.1038/372525a0openalex-snapshot
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
inferredcites →https://doi.org/10.1038/74155openalex-snapshot
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
inferredcites →https://doi.org/10.1038/76074openalex-snapshot
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
inferredcites →https://doi.org/10.1038/9718openalex-snapshot
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
inferredcites →https://doi.org/10.1038/ejhg.2008.149openalex-snapshot
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
inferredcites →https://doi.org/10.1038/ejhg.2008.245openalex-snapshot
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P
inferredcites →https://doi.org/10.1038/nature08451openalex-snapshot
Genomic views of distant-acting enhancers
inferredcites →https://doi.org/10.1038/ng.2007.55openalex-snapshot
Ultraconservation identifies a small subset of extremely constrained developmental enhancers
inferredcites →https://doi.org/10.1038/ng.242openalex-snapshot
Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
inferredcites →https://doi.org/10.1038/ng.329openalex-snapshot
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
inferredcites →https://doi.org/10.1038/ng.333openalex-snapshot
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
inferredcites →https://doi.org/10.1038/ng.499openalex-snapshot
Exome sequencing identifies the cause of a mendelian disorder
inferredcites →https://doi.org/10.1038/ng.506openalex-snapshot
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
inferredcites →https://doi.org/10.1038/ng.580openalex-snapshot
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
inferredcites →https://doi.org/10.1038/ng.646openalex-snapshot
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
inferredcites →https://doi.org/10.1038/ng.82openalex-snapshot
MicroRNA Mirn140 modulates Pdgf signaling during palatogenesis
inferredcites →https://doi.org/10.1038/ng0197-36openalex-snapshot
Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome
inferredcites →https://doi.org/10.1038/ng0197-42openalex-snapshot
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
inferredcites →https://doi.org/10.1038/ng0295-165openalex-snapshot
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
inferredcites →https://doi.org/10.1038/ng0494-348openalex-snapshot
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
inferredcites →https://doi.org/10.1038/ng0994-98openalex-snapshot
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
inferredcites →https://doi.org/10.1038/ng1122openalex-snapshot
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
inferredcites →https://doi.org/10.1038/ng1196-357openalex-snapshot
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly
inferredcites →https://doi.org/10.1038/ng1197-285openalex-snapshot
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
inferredcites →https://doi.org/10.1038/ng1264openalex-snapshot
Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation
inferredcites →https://doi.org/10.1038/ng1319openalex-snapshot
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis
inferredcites →https://doi.org/10.1038/ng1321openalex-snapshot
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR
inferredcites →https://doi.org/10.1038/ng1363openalex-snapshot
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
inferredcites →https://doi.org/10.1038/ng1407openalex-snapshot
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
inferredcites →https://doi.org/10.1038/ng1415openalex-snapshot
A specific requirement for PDGF-C in palate formation and PDGFR-α signaling
inferredcites →https://doi.org/10.1038/ng1511openalex-snapshot
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
inferredcites →https://doi.org/10.1038/ng1548openalex-snapshot
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
inferredcites →https://doi.org/10.1038/ng1894openalex-snapshot
Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch
inferredcites →https://doi.org/10.1038/ng1903openalex-snapshot
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)
inferredcites →https://doi.org/10.1038/ng730openalex-snapshot
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
inferredcites →https://doi.org/10.1038/ng740openalex-snapshot
Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela
inferredcites →https://doi.org/10.1038/ng985openalex-snapshot
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
inferredcites →https://doi.org/10.1038/sj.ejhg.5201486openalex-snapshot
Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population
inferredcites →https://doi.org/10.1056/nejmoa032909openalex-snapshot
Interferon Regulatory Factor 6 ( IRF6 ) Gene Variants and the Risk of Isolated Cleft Lip or Palate
inferredcites →https://doi.org/10.1056/nejmoa0907328openalex-snapshot
Valproic Acid Monotherapy in Pregnancy and Major Congenital Malformations
inferredcites →https://doi.org/10.1056/nejmoa0908094openalex-snapshot
Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy
inferredcites →https://doi.org/10.1067/s0022-3476(03)00495-5openalex-snapshot
Association between folic acid food fortification and congenital orofacial clefts
inferredcites →https://doi.org/10.1073/pnas.0607956104openalex-snapshot
Impaired FGF signaling contributes to cleft lip and palate
inferredcites →https://doi.org/10.1073/pnas.2235734100openalex-snapshot
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features
inferredcites →https://doi.org/10.1086/301936openalex-snapshot
Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome
inferredcites →https://doi.org/10.1086/301956openalex-snapshot
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans
inferredcites →https://doi.org/10.1086/316915openalex-snapshot
Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
inferredcites →https://doi.org/10.1086/318802openalex-snapshot
Identification of the Gene for Oral-Facial-Digital Type I Syndrome
inferredcites →https://doi.org/10.1086/323473openalex-snapshot
Mutations in the 3β-Hydroxysterol Δ24-Reductase Gene Cause Desmosterolosis, an Autosomal Recessive Disorder of Cholesterol Biosynthesis
inferredcites →https://doi.org/10.1086/382196openalex-snapshot
Homozygous WNT3 Mutation Causes Tetra-Amelia in a Large Consanguineous Family
inferredcites →https://doi.org/10.1086/427344openalex-snapshot
Strong Evidence of Linkage Disequilibrium between Polymorphisms at the IRF6 Locus and Nonsyndromic Cleft Lip With or Without Cleft Palate, in an Italian Population
inferredcites →https://doi.org/10.1086/506256openalex-snapshot
Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome
inferredcites →https://doi.org/10.1086/510518openalex-snapshot
Orofacial Cleft Risk Is Increased with Maternal Smoking and Specific Detoxification-Gene Variants
inferredcites →https://doi.org/10.1089/dna.2009.0935openalex-snapshot
Association Among Polymorphisms at MYH9 , Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China
inferredcites →https://doi.org/10.1089/gtmb.2009.0052openalex-snapshot
Mutation Analysis of the PVRL1 Gene in Caucasians with Nonsyndromic Cleft Lip/Palate
inferredcites →https://doi.org/10.1093/aje/kwi214openalex-snapshot
Cleft Lip and Palate versus Cleft Lip Only: Are They Distinct Defects?
inferredcites →https://doi.org/10.1093/aje/kwn186openalex-snapshot
First-Trimester Maternal Alcohol Consumption and the Risk of Infant Oral Clefts in Norway: A Population-based Case-Control Study
inferredcites →https://doi.org/10.1093/aje/kwq226openalex-snapshot
Maternal Alcohol Consumption, Alcohol Metabolism Genes, and the Risk of Oral Clefts: A Population-based Case-Control Study in Norway, 1996-2001
inferredcites →https://doi.org/10.1093/hmg/10.3.221openalex-snapshot
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
inferredcites →https://doi.org/10.1093/hmg/ddg248openalex-snapshot
Identification of SATB2 as the cleft palate gene on 2q32-q33
inferredcites →https://doi.org/10.1093/hmg/ddi157openalex-snapshot
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1
inferredcites →https://doi.org/10.1093/hmg/ddm176openalex-snapshot
CRISPLD2: a novel NSCLP candidate gene
inferredcites →https://doi.org/10.1093/hmg/ddn121openalex-snapshot
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate
inferredcites →https://doi.org/10.1093/hmg/ddp201openalex-snapshot
Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence
inferredcites →https://doi.org/10.1093/hmg/ddp368openalex-snapshot
Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes
inferredcites →https://doi.org/10.1093/hmg/ddp444openalex-snapshot
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
inferredcites →https://doi.org/10.1093/hmg/ddq223openalex-snapshot
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes
inferredcites →https://doi.org/10.1093/ije/dyn098openalex-snapshot
Folate intake, markers of folate status and oral clefts: is the evidence converging?
inferredcites →https://doi.org/10.1093/oso/9780195139068.003.0019openalex-snapshot
Mode of Inheritance of Oral Clefts
inferredcites →https://doi.org/10.1097/00001648-200109000-00007openalex-snapshot
Smoking, Genetic Polymorphisms in Biotransformation Enzymes, and Nonsyndromic Oral Clefting: A Gene-Environment Interaction
inferredcites →https://doi.org/10.1097/00125817-200201000-00001openalex-snapshot
Structural brain abnormalities in adult males with clefts of the lip and/or palate
inferredcites →https://doi.org/10.1097/01.ede.0000112214.33432.ccopenalex-snapshot
Maternal Smoking and the Risk of Orofacial Clefts
inferredcites →https://doi.org/10.1097/01.gim.0000127275.52925.05openalex-snapshot
In a Vietnamese population, MSX1 variants contribute to cleft lip and palate
inferredcites →https://doi.org/10.1097/gim.0b013e3180423ccaopenalex-snapshot
Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations
inferredcites →https://doi.org/10.1097/gim.0b013e3181833793openalex-snapshot
Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts
inferredcites →https://doi.org/10.1097/scs.0b013e3181ec6aadopenalex-snapshot
Wound Complications After Cleft Repair in Children With Van der Woude Syndrome
inferredcites →https://doi.org/10.1101/gad.13.23.3106openalex-snapshot
Vax1, a novel homeobox-containing gene, directs development of the basal forebrain and visual system
inferredcites →https://doi.org/10.1111/j.1399-0004.2009.01174.xopenalex-snapshot
Importance of gene–environment interactions in the etiology of selected birth defects
inferredcites →https://doi.org/10.1111/j.1600-0722.2010.00729.xopenalex-snapshot
MTHFRandMSX1contribute to the risk of nonsyndromic cleft lip/palate
inferredcites →https://doi.org/10.1111/j.1601-0825.2009.01577.xopenalex-snapshot
The genetics of isolated orofacial clefts: from genotypes to subphenotypes
inferredcites →https://doi.org/10.1111/j.1601-0825.2009.01587.xopenalex-snapshot
Folic acid and orofacial clefts: a review of the evidence
inferredcites →https://doi.org/10.1111/j.1601-0825.2009.01588.xopenalex-snapshot
The impact of orofacial clefts on quality of life and healthcare use and costs
inferredcites →https://doi.org/10.1111/j.1601-6343.2007.00386.xopenalex-snapshot
Subclinical features in non‐syndromic cleft lip with or without cleft palate (CL/P): review of the evidence that subepithelial orbicularis oris muscle defects are part of an expanded phenotype for CL/P*
inferredcites →https://doi.org/10.1111/j.1601-6343.2009.01462.xopenalex-snapshot
Face shape of unaffected parents with cleft affected offspring: combining three‐dimensional surface imaging and geometric morphometrics
inferredcites →https://doi.org/10.1126/science.1068206openalex-snapshot
Optical Projection Tomography as a Tool for 3D Microscopy and Gene Expression Studies
inferredcites →https://doi.org/10.1126/science.1128406openalex-snapshot
SUMO1 Haploinsufficiency Leads to Cleft Lip and Palate
inferredcites →https://doi.org/10.1126/science.1186802openalex-snapshot
Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
inferredcites →https://doi.org/10.1126/science.272.5268.1668openalex-snapshot
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
inferredcites →https://doi.org/10.1136/bmj.38106.559120.7copenalex-snapshot
Long term follow up study of survival associated with cleft lip and palate at birth
inferredcites →https://doi.org/10.1136/bmj.39079.618287.0bopenalex-snapshot
Folic acid supplements and risk of facial clefts: national population based case-control study
inferredcites →https://doi.org/10.1136/jmg.2004.029439openalex-snapshot
Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate
inferredcites →https://doi.org/10.1136/jmg.2005.031385openalex-snapshot
Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer
inferredcites →https://doi.org/10.1136/jmg.2006.047837openalex-snapshot
Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA
inferredcites →https://doi.org/10.1136/jmg.2007.052191openalex-snapshot
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
inferredcites →https://doi.org/10.1136/jmg.2009.069385openalex-snapshot
A cohort study of recurrence patterns among more than 54 000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance
inferredcites →https://doi.org/10.1136/jmg.31.2.126openalex-snapshot
Facial clefts in the west of Scotland in the period 1980-1984: epidemiology and genetic diagnoses.
inferredcites →https://doi.org/10.1136/jmg.36.5.353openalex-snapshot
Clinical and molecular genetics of Stickler syndrome
inferredcites →https://doi.org/10.1136/jmg.40.6.399openalex-snapshot
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
inferredcites →https://doi.org/10.1159/000150783openalex-snapshot
THOUGHTS ON THE ETIOLOGY OF CLEFTS OF THE PALATE AND LIP
inferredcites →https://doi.org/10.1159/000224636openalex-snapshot
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
inferredcites →https://doi.org/10.1172/jci29872openalex-snapshot
Cholesterol precursors and facial clefting
inferredcites →https://doi.org/10.1172/jci40266openalex-snapshot
Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice
inferredcites →https://doi.org/10.1177/154405910308200409openalex-snapshot
MSX1 and TGFB3 Contribute to Clefting in South America
inferredcites →https://doi.org/10.1203/pdr.0b013e3181cbd564openalex-snapshot
Autoantibodies to Folate Receptor α During Early Pregnancy and Risk of Oral Clefts in Denmark
inferredcites →https://doi.org/10.1242/dev.01676openalex-snapshot
Distinct functions for Bmp signaling in lip and palate fusion in mice
inferredcites →https://doi.org/10.1242/dev.037440openalex-snapshot
Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion
inferredcites →https://doi.org/10.1242/dev.129.17.4135openalex-snapshot
Rescue of cleft palate inMsx1-deficient mice by transgenicBmp4reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis
inferredcites →https://doi.org/10.1371/journal.pbio.1000294openalex-snapshot
Rare Variants Create Synthetic Genome-Wide Associations
inferredcites →https://doi.org/10.1371/journal.pgen.0010064openalex-snapshot
Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate
inferredcites →https://doi.org/10.1371/journal.pone.0005385openalex-snapshot
Genetic Determinants of Facial Clefting: Analysis of 357 Candidate Genes Using Two National Cleft Studies from Scandinavia
inferredcites →https://doi.org/10.14219/jada.archive.2009.0022openalex-snapshot
AXIS inhibition protein 2, orofacial clefts and a family history of cancer
inferredcites →https://doi.org/10.1597/03-139.1openalex-snapshot
Changing Lifestyles and Oral Clefts Occurrence in Denmark
inferredcites →https://doi.org/10.1597/06-002openalex-snapshot
Prevention of Orofacial Clefts: Does Pregnancy Planning Have a Role?
inferredcites →https://doi.org/10.1597/07-115.1openalex-snapshot
Anatomical Basis for Apparent Subepithelial Cleft Lip: A Histological and Ultrasonographic Survey of the Orbicularis Oris Muscle
inferredcites →https://doi.org/10.1597/08-228openalex-snapshot
Cerebellum Structure Differences and Relationship to Speech in Boys and Girls with Nonsyndromic Cleft of the Lip and/or Palate
inferredcites →https://doi.org/10.1597/09-015openalex-snapshot
Association between TGFB3 and Nonsyndromic Cleft Lip with or Without Cleft Palate in a Chilean Population
inferredcites →https://doi.org/10.1597/09-153openalex-snapshot
Ethnic Heterogeneity of IRF6 AP-2a Binding Site Promoter SNP Association with Nonsyndromic Cleft Lip and Palate
inferredcites →https://doi.org/10.1597/09-227openalex-snapshot
CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip with or without Cleft Palate
inferredcites →https://doi.org/10.1597/09-245openalex-snapshot
Reproductive Patterns among Danish Women with Oral Clefts
inferredcites →https://doi.org/10.1597/1545-1569(2002)039<0149:nclwow>2.0.co;2openalex-snapshot
Nonsyndromic Cleft Lip With or Without Cleft Palate in China: Assessment of Candidate Regions
inferredcites →https://doi.org/10.4103/0970-0358.57182openalex-snapshot
Addressing the challenges of cleft lip and palate research in India
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3991629openalex-extracted
Abnormal Structure in Lip Area Cortex of Mother With Cleft Lip Fetus
inferred← citeshttps://doi.org/10.1001/jamapediatrics.2013.4858openalex-snapshot
Genetic Epidemiology and Nonsyndromic Structural Birth Defects
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020915.pub2openalex-snapshot
Craniofacial Defects and Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026602openalex-snapshot
Vertebrate Embryo: Craniofacial Development
inferred← citeshttps://doi.org/10.1002/9781118925263.ch04openalex-snapshot
The genetics of the dental occlusion and malocclusion
inferred← citeshttps://doi.org/10.1002/9781119004370.ch55openalex-snapshot
Developmental Disorders of the Craniofacial Complex
inferred← citeshttps://doi.org/10.1002/9781119778387.ch3openalex-snapshot
Embryology and classification of orofacial clefting
inferred← citeshttps://doi.org/10.1002/9781119778387.ch48openalex-snapshot
Application of artificial intelligence in treating patients with cleft and craniofacial anomalies
inferred← citeshttps://doi.org/10.1002/9781119912576.ch4openalex-snapshot
The genetics of the dental occlusion and malocclusion
inferred← citeshttps://doi.org/10.1002/advs.202412073openalex-snapshot
Exome Sequencing Reveals the Genetic Architecture of Non‐syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene
inferred← citeshttps://doi.org/10.1002/advs.202504191openalex-snapshot
Single‐Nucleus RNA Sequencing Reveals Mid‐Gestational Neurodevelopment Features in the Superior Temporal Plane from Fetuses with Nonsyndromic Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.34169openalex-snapshot
Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population
inferred← citeshttps://doi.org/10.1002/ajmg.a.35257openalex-snapshot
Genome wide study of maternal and parent‐of‐origin effects on the etiology of orofacial clefts
inferred← citeshttps://doi.org/10.1002/ajmg.a.35526openalex-snapshot
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
inferred← citeshttps://doi.org/10.1002/ajmg.a.35641openalex-snapshot
Association of interactions among the IRF6 gene, the 8q24 region, and maternal folic acid intake with non‐syndromic cleft lip/palate in Mexican Mestizos
inferred← citeshttps://doi.org/10.1002/ajmg.a.35749openalex-snapshot
Replication of Genome Wide Association Identified Candidate Genes Confirm the Role of Common and Rare Variants in PAX 7and VAX 1in the Etiology of Nonsyndromic CL(P)
inferred← citeshttps://doi.org/10.1002/ajmg.a.35835openalex-snapshot
Corpus Callosum Shape Is Altered in Individuals With Nonsyndromic Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.36133openalex-snapshot
Search for genetic modifiers of IRF6 and genotype–phenotype correlations in Van der Woude and popliteal pterygium syndromes
inferred← citeshttps://doi.org/10.1002/ajmg.a.36186openalex-snapshot
Risk of nonsyndromic cleft lip and palate in relatives of women with breast cancer
inferred← citeshttps://doi.org/10.1002/ajmg.a.36691openalex-snapshot
Rare functional variants in genome–wide association identified candidate genes for nonsyndromic clefts in the African population
inferred← citeshttps://doi.org/10.1002/ajmg.a.36693openalex-snapshot
Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians
inferred← citeshttps://doi.org/10.1002/ajmg.a.36802openalex-snapshot
Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.36839openalex-snapshot
Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene
inferred← citeshttps://doi.org/10.1002/ajmg.a.36891openalex-snapshot
A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.36896openalex-snapshot
Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders
inferred← citeshttps://doi.org/10.1002/ajmg.a.36912openalex-snapshot
Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans
inferred← citeshttps://doi.org/10.1002/ajmg.a.37181openalex-snapshot
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry
inferred← citeshttps://doi.org/10.1002/ajmg.a.37281openalex-snapshot
Interactions between RAD51 rs1801321 and maternal cigarette smoking as risk factor for nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.37561openalex-snapshot
TPM1 polymorphisms and nonsyndromic orofacial clefts susceptibility in a Chinese Han population
inferred← citeshttps://doi.org/10.1002/ajmg.a.37874openalex-snapshot
Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.38190openalex-snapshot
Gene‐gene interaction of single nucleotide polymorphisms in 16p13.3 may contribute to the risk of non‐syndromic cleft lip with or without cleft palate in Chinese case‐parent trios
inferred← citeshttps://doi.org/10.1002/ajmg.a.38210openalex-snapshot
Association studies of low‐frequency coding variants in nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.38471openalex-snapshot
Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting
inferred← citeshttps://doi.org/10.1002/ajmg.a.38634openalex-snapshot
ICD‐10 impact on ascertainment and accuracy of oral cleft cases as recorded by the Brazilian national live birth information system
inferred← citeshttps://doi.org/10.1002/ajmg.a.38688openalex-snapshot
Soft tissue nasal asymmetry as an indicator of orofacial cleft predisposition
inferred← citeshttps://doi.org/10.1002/ajmg.a.61183openalex-snapshot
Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/ajmg.a.61834openalex-snapshot
Prevalence rates study of selected isolated non‐Mendelian congenital anomalies in the Hutterite population of Alberta, 1980–2016
inferred← citeshttps://doi.org/10.1002/ajmg.a.62689openalex-snapshot
Co‐occurring anomalies in congenital oral clefts
inferred← citeshttps://doi.org/10.1002/ajmg.a.63015openalex-snapshot
Identification of a new familial case of 3q29 deletion syndrome associated with cleft lip and palate via whole‐exome sequencing
inferred← citeshttps://doi.org/10.1002/ajmg.a.63101openalex-snapshot
Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10
inferred← citeshttps://doi.org/10.1002/ajmg.a.63336openalex-snapshot
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
inferred← citeshttps://doi.org/10.1002/ajmg.c.31379openalex-snapshot
Genomic approaches for studying craniofacial disorders
inferred← citeshttps://doi.org/10.1002/ajmg.c.31381openalex-snapshot
Genetics of cleft lip and cleft palate
inferred← citeshttps://doi.org/10.1002/ar.24076openalex-snapshot
In Vitro Analysis of Palatal Shelf Elevation During Secondary Palate Formation
inferred← citeshttps://doi.org/10.1002/ar.24111openalex-snapshot
Breaking Symmetry: A Quantitative Analysis of Facial Skeleton Disharmony in Children Born with Bilateral Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/ar.24547openalex-snapshot
Cellular and molecular mechanisms in the development of a cleft lip and/or cleft palate; insights from zebrafish ( Danio rerio )
inferred← citeshttps://doi.org/10.1002/bdr2.1054openalex-snapshot
Chromosome copy number variants in fetuses with syndromic malformations
inferred← citeshttps://doi.org/10.1002/bdr2.1063openalex-snapshot
Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population
inferred← citeshttps://doi.org/10.1002/bdr2.1123openalex-snapshot
CranFlow: An Application for Record‐Taking and Management Through the Brazilian Database on Craniofacial Anomalies
inferred← citeshttps://doi.org/10.1002/bdr2.1188openalex-snapshot
Plasma zinc levels in Ecuadorian mothers of infants with nonsyndromic cleft lip with or without cleft palate: A case series
inferred← citeshttps://doi.org/10.1002/bdr2.1208openalex-snapshot
Potential genetic markers for nonsyndromic oral clefts in the Brazilian population: A systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1002/bdr2.1346openalex-snapshot
BRCA1 and BRCA2 gene variants and nonsyndromic cleft lip/palate
inferred← citeshttps://doi.org/10.1002/bdr2.1405openalex-snapshot
Understanding the participation of GREM1 polymorphisms in nonsyndromic cleft lip with or without cleft palate in the Brazilian population
inferred← citeshttps://doi.org/10.1002/bdr2.1467openalex-snapshot
Birth prevalence of orofacial clefts among perinatal infants: A register‐based study in Bao'an district, Shenzhen, China
inferred← citeshttps://doi.org/10.1002/bdr2.1473openalex-snapshot
Understanding chondrodysplasia (cho): A comprehensive review of cho as an animal model of birth defects, disorders, and molecular mechanisms
inferred← citeshttps://doi.org/10.1002/bdr2.1504openalex-snapshot
Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/bdr2.1564openalex-snapshot
Nucleic acid methylation and orofacial morphogenesis
inferred← citeshttps://doi.org/10.1002/bdr2.1581openalex-snapshot
Characterizing cleft palate toxicants using ToxCast data, chemical structure, and the biomedical literature
inferred← citeshttps://doi.org/10.1002/bdr2.1630openalex-snapshot
PBX‐WNT‐P63‐IRF6pathway in nonsyndromic cleft lip and palate
inferred← citeshttps://doi.org/10.1002/bdr2.1802openalex-snapshot
Role of epigenetics and miRNAs in orofacial clefts
inferred← citeshttps://doi.org/10.1002/bdr2.1959openalex-snapshot
MTHFR promoter methylation might mitigate the effect of smoking at the level of LINE ‐1 in cleft lip tissues: A preliminary study
inferred← citeshttps://doi.org/10.1002/bdr2.2102openalex-snapshot
DNA methylation profile of lip tissue from congenital nonsyndromic cleft lip and palate patients by whole‐genome bisulfite sequencing
inferred← citeshttps://doi.org/10.1002/bdr2.2216openalex-snapshot
Ezh2‐dependent methylation in oral epithelia promotes secondary palatogenesis
inferred← citeshttps://doi.org/10.1002/bdr2.2226openalex-snapshot
Epigenetic implications in maternal diabetes and metabolic syndrome‐associated risk of orofacial clefts
inferred← citeshttps://doi.org/10.1002/bdr2.2229openalex-snapshot
An improved multicellular human organoid model for the study of chemical effects on palatal fusion
inferred← citeshttps://doi.org/10.1002/bdr2.2244openalex-snapshot
Retinoic acid delays murine palatal shelf elevation by inhibiting Wnt5a‐mediated noncanonical Wnt signaling and downstream Cdc‐42/F‐actin remodeling in mesenchymal cells
inferred← citeshttps://doi.org/10.1002/bdr2.2288openalex-snapshot
Genetic variants in BCL ‐2 family genes influence the risk of non‐syndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/bdr2.2295openalex-snapshot
Publicly funded healthcare costs associated with orofacial clefts for children born in Alberta, Canada between 2002 and 2018
inferred← citeshttps://doi.org/10.1002/bdr2.23605openalex-snapshot
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing
inferred← citeshttps://doi.org/10.1002/bdr2.2387openalex-snapshot
Orofacial clefts in Costa Rica, 1996–2021: Analysis of surveillance data
inferred← citeshttps://doi.org/10.1002/bdr2.2403openalex-snapshot
Genetic Variants in METTL16 Affect the Risk of Non‐Syndromic Orofacial Clefts
inferred← citeshttps://doi.org/10.1002/bdr2.2467openalex-snapshot
Integrated Transcriptomic and Metabolomic Profiling of the Placenta in a Dexamethasone‐Induced Cleft Palate Rabbit Model
inferred← citeshttps://doi.org/10.1002/bdr2.2499openalex-snapshot
Functional Annotation of De Novo Variants Found Near GWAS Loci Associated With Cleft Lip With or Without Cleft Palate
inferred← citeshttps://doi.org/10.1002/bdr2.2528openalex-snapshot
Cancer Risk and Genetic Associations in Individuals With Cleft Lip and Palate and Their Families: A Narrative Review
inferred← citeshttps://doi.org/10.1002/bdr2.70079openalex-snapshot
Prevalence, Temporal Trends, Diversity, and Associated Risk Factors of Isolated Cleft Lip With or Without Cleft Palate: A 20‐Year Retrospective Hospital‐Based Study in Iran (2003–2023)
inferred← citeshttps://doi.org/10.1002/bdra.20843openalex-snapshot
Polymorphisms of stress‐related genes and the risk of nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/bdra.22862openalex-snapshot
Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non‐syndromic cleft lip and palate in the polish population
inferred← citeshttps://doi.org/10.1002/bdra.22879openalex-snapshot
Nine new twin pairs with esophageal atresia: A review of the literature and performance of a twin study of the disorder
inferred← citeshttps://doi.org/10.1002/bdra.23011openalex-snapshot
Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil
inferred← citeshttps://doi.org/10.1002/bdra.23026openalex-snapshot
Association of MMP3 and TIMP2 promoter polymorphisms with nonsyndromic oral clefts
inferred← citeshttps://doi.org/10.1002/bdra.23056openalex-snapshot
Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a polish population
inferred← citeshttps://doi.org/10.1002/bdra.23076openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/bdra.23114openalex-snapshot
Thymidylate synthase polymorphisms and risks of human orofacial clefts
inferred← citeshttps://doi.org/10.1002/bdra.23133openalex-snapshot
Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled‐analysis
inferred← citeshttps://doi.org/10.1002/bdra.23173openalex-snapshot
Factors associated with distance and time traveled to cleft and craniofacial care
inferred← citeshttps://doi.org/10.1002/bdra.23199openalex-snapshot
MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the Brazilian population
inferred← citeshttps://doi.org/10.1002/bdra.23204openalex-snapshot
Analysis of susceptibility polymorphisms for nonsyndromic cleft lip with or without cleft palate in the Brazilian population
inferred← citeshttps://doi.org/10.1002/bdra.23214openalex-snapshot
Oral cleft recurrence risk and subsequent maternal fertility preferences and behavior in Brazil
inferred← citeshttps://doi.org/10.1002/bdra.23248openalex-snapshot
Corticosteroid use and risk of orofacial clefts
inferred← citeshttps://doi.org/10.1002/bdra.23286openalex-snapshot
Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate
inferred← citeshttps://doi.org/10.1002/bdra.23320openalex-snapshot
Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain
inferred← citeshttps://doi.org/10.1002/bdra.23362openalex-snapshot
A genome‐wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts
inferred← citeshttps://doi.org/10.1002/bdra.23365openalex-snapshot
rs1801133C>T polymorphism in MTHFR is a risk factor for nonsyndromic cleft lip with or without cleft palate in the Brazilian population
inferred← citeshttps://doi.org/10.1002/bdra.23391openalex-snapshot
Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population
inferred← citeshttps://doi.org/10.1002/bdra.23413openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/bdra.23417openalex-snapshot
Parental risk factors for oral clefts among Central Africans, Southeast Asians, and Central Americans
inferred← citeshttps://doi.org/10.1002/bdra.23454openalex-snapshot
Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population
inferred← citeshttps://doi.org/10.1002/bdra.23540openalex-snapshot
Association between IRF6 and 8q24 polymorphisms and nonsyndromic cleft lip with or without cleft palate: Systematic review and meta‐analysis
inferred← citeshttps://doi.org/10.1002/bdra.23546openalex-snapshot
Inhibition of the 3‐hydroxy‐3‐methyl‐glutaryl‐CoA reductase induces orofacial defects in zebrafish
inferred← citeshttps://doi.org/10.1002/bdra.23596openalex-snapshot
Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate
inferred← citeshttps://doi.org/10.1002/bdra.23605openalex-snapshot
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing
inferred← citeshttps://doi.org/10.1002/bdra.23612openalex-snapshot
Associations between the NOGGIN rs227731 polymorphism and NSCL/P risk may be associated with ethnicities: A meta‐analysis
inferred← citeshttps://doi.org/10.1002/cga.70036openalex-snapshot
The Suggestive Association Between the NOG rs227731 Polymorphism and Non‐Syndromic Cleft Lip With or Without Palate Subtypes in a Japanese Cohort
inferred← citeshttps://doi.org/10.1002/cga.70069openalex-snapshot
Folic Acid Alleviates X‐Ray Irradiation‐Induced Jaw Malformation in Zebrafish
inferred← citeshttps://doi.org/10.1002/cga.70071openalex-snapshot
Evaluating the Role of VAX1 , MAFB , and NOG in Non‐Syndromic Cleft Palate Only Among Japanese Individuals
inferred← citeshttps://doi.org/10.1002/cga.70072openalex-snapshot
The Near‐Absence of Isolated Cleft Palate in a Surgical Mission Cohort in Ethiopia: Implications for Infant Mortality and Disease Recognition
inferred← citeshttps://doi.org/10.1002/cga.70081openalex-snapshot
Epidemiological Investigation of Sex Differences by Cleft Phenotype and Extent in Cleft Lip and/or Palate: The Cohort Study of 4548 Japanese Patients
inferred← citeshttps://doi.org/10.1002/dvdy.179openalex-snapshot
Chemical‐induced craniofacial anomalies caused by disruption of neural crest cell development in a zebrafish model
inferred← citeshttps://doi.org/10.1002/dvdy.22713openalex-snapshot
Examination of a palatogenic gene program in zebrafish
inferred← citeshttps://doi.org/10.1002/dvdy.23862openalex-snapshot
The regulation of endogenous retinoic acid level through CYP26B1 is required for elevation of palatal shelves
inferred← citeshttps://doi.org/10.1002/dvdy.23867openalex-snapshot
Cleft palate defect of Dlx1/2 −/− mutant mice is caused by lack of vertical outgrowth in the posterior palate
inferred← citeshttps://doi.org/10.1002/dvdy.23969openalex-snapshot
A morpholino‐based screen to identify novel genes involved in craniofacial morphogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.24095openalex-snapshot
Embryonic craniofacial bone volume and bone mineral density in Fgfr2+/P253R and nonmutant mice
inferred← citeshttps://doi.org/10.1002/dvdy.24319openalex-snapshot
Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation
inferred← citeshttps://doi.org/10.1002/dvdy.24320openalex-snapshot
Sox10ERT2CreERT2 mice enable tracing of distinct neural crest cell populations
inferred← citeshttps://doi.org/10.1002/dvdy.24338openalex-snapshot
Recent insights into the morphological diversity in the amniote primary and secondary palates
inferred← citeshttps://doi.org/10.1002/dvdy.24403openalex-snapshot
Pdgfra and Pdgfrb genetically interact during craniofacial development
inferred← citeshttps://doi.org/10.1002/dvdy.24566openalex-snapshot
Zebrafish models of orofacial clefts
inferred← citeshttps://doi.org/10.1002/dvdy.327openalex-snapshot
The Mafb cleft‐associated variant H131Q is not required for palatogenesis in the mouse
inferred← citeshttps://doi.org/10.1002/dvdy.4openalex-snapshot
Craniofacial skeleton of MEXICAN tetra (Astyanax mexicanus): As a bone disease model
inferred← citeshttps://doi.org/10.1002/dvdy.573openalex-snapshot
Single cell sequencing of the mouse anterior palate reveals mesenchymal heterogeneity
inferred← citeshttps://doi.org/10.1002/dvdy.745openalex-snapshot
foxe1 mutant zebrafish show indications of a hypothyroid phenotype and increased sensitivity to ethanol for craniofacial malformations
inferred← citeshttps://doi.org/10.1002/dvg.23441openalex-snapshot
Sox9CreER ‐mediated deletion of β‐catenin in palatal mesenchyme results in delayed palatal elevation accompanied with repressed canonical Wnt signaling and reduced actin polymerization
inferred← citeshttps://doi.org/10.1002/em.22239openalex-snapshot
Interactions between superoxide dismutase and paraoxonase polymorphic variants in nonsyndromic cleft lip with or without cleft palate in the Brazilian population
inferred← citeshttps://doi.org/10.1002/em.22286openalex-snapshot
Exploring the interaction between FGF Genes and T‐box genes among chinese nonsyndromic cleft lip with or without cleft palate case‐parent trios
inferred← citeshttps://doi.org/10.1002/emmm.201200202openalex-snapshot
p63 and FGFR: when development meets proliferation
inferred← citeshttps://doi.org/10.1002/gepi.21972openalex-snapshot
Using Whole Exome Sequencing to Identify Candidate Genes With Rare Variants In Nonsyndromic Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/gepi.21987openalex-snapshot
A Clustered Multiclass Likelihood‐Ratio Ensemble Method for Family‐Based Association Analysis Accounting for Phenotypic Heterogeneity
inferred← citeshttps://doi.org/10.1002/gepi.22023openalex-snapshot
Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios
inferred← citeshttps://doi.org/10.1002/gepi.22090openalex-snapshot
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
inferred← citeshttps://doi.org/10.1002/gepi.22158openalex-snapshot
Genome‐wide interaction studies identify sex‐specific risk alleles for nonsyndromic orofacial clefts
inferred← citeshttps://doi.org/10.1002/gepi.22214openalex-snapshot
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals
inferred← citeshttps://doi.org/10.1002/gepi.22343openalex-snapshot
Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms
inferred← citeshttps://doi.org/10.1002/gepi.22447openalex-snapshot
Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
inferred← citeshttps://doi.org/10.1002/gepi.22453openalex-snapshot
Benchmarking statistical methods for analyzing parent–child dyads in genetic association studies
inferred← citeshttps://doi.org/10.1002/hec.2901openalex-snapshot
FETAL HEALTH SHOCKS AND EARLY INEQUALITIES IN HEALTH CAPITAL ACCUMULATION
inferred← citeshttps://doi.org/10.1002/humu.23415openalex-snapshot
A functional polymorphism in the pre-miR-146a gene is associated with the risk of nonsyndromic orofacial cleft
inferred← citeshttps://doi.org/10.1002/humu.23793openalex-snapshot
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans
inferred← citeshttps://doi.org/10.1002/humu.24473openalex-snapshot
Mutations in the TBX15‐ADAMTS2 pathway associate with a novel soft palate dysplasia
inferred← citeshttps://doi.org/10.1002/jbm.a.34062openalex-snapshot
Indirect coating of RGD peptides using a poly‐ L ‐lysine spacer enhances jaw periosteal cell adhesion, proliferation, and differentiation into osteogenic tissue
inferred← citeshttps://doi.org/10.1002/jbm.a.36430openalex-snapshot
A caninein vitromodel for evaluation of marrow‐derived mesenchymal stromal cell‐based bone scaffolds
inferred← citeshttps://doi.org/10.1002/jcb.24417openalex-snapshot
Identification of candidate downstream targets of TGFβ signaling during palate development by genome‐wide transcript profiling
inferred← citeshttps://doi.org/10.1002/jcb.27320openalex-snapshot
Correlation between HDAC4 enhancer DNA methylation and mRNA expression during palatal fusion induced by all‐trans retinoic acid
inferred← citeshttps://doi.org/10.1002/jcb.28888openalex-snapshot
Identification of circular RNA‐associated competing endogenous RNA network in the development of cleft palate
inferred← citeshttps://doi.org/10.1002/jcla.22428openalex-snapshot
Application of high‐resolution array platform for genome‐wide copy number variation analysis in patients with nonsyndromic cleft lip and palate
inferred← citeshttps://doi.org/10.1002/jgm.3531openalex-snapshot
High throughput miRNA sequencing and bioinformatics analysis identify the mesenchymal cell proliferation and apoptosis related miRNAs during fetal mice palate development
inferred← citeshttps://doi.org/10.1002/jmor.70032openalex-snapshot
On the Maxillofacial Development of Mice, Mus musculus
inferred← citeshttps://doi.org/10.1002/jum.70432openalex-snapshot
Prenatal Ultrasonic Detection of Fetal Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/lary.23394openalex-snapshot
Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations
inferred← citeshttps://doi.org/10.1002/lary.25022openalex-snapshot
Cholesteatoma risk in 8,593 orofacial cleft cases and 6,989 siblings: A nationwide study
inferred← citeshttps://doi.org/10.1002/lary.26637openalex-snapshot
ACSS2 gene variant associated with cleft lip and palate in two independent Hispanic populations
inferred← citeshttps://doi.org/10.1002/lary.29209openalex-snapshot
Malnutrition as a Risk Factor in Cleft Lip and Palate Surgery
inferred← citeshttps://doi.org/10.1002/lary.29899openalex-snapshot
Demographic Risk Factors for Malnutrition in Patients With Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1002/lary.31267openalex-snapshot
Children's Visual Perception of Facial Scarring and Cleft Lip Deformity Using Eye Tracking Data
inferred← citeshttps://doi.org/10.1002/med.21594openalex-snapshot
Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
inferred← citeshttps://doi.org/10.1002/mgg3.1196openalex-snapshot
Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome
inferred← citeshttps://doi.org/10.1002/mgg3.155openalex-snapshot
Regulatory variant in FZD 6gene contributes to nonsyndromic cleft lip and palate in an African‐American family
inferred← citeshttps://doi.org/10.1002/mgg3.1655openalex-snapshot
Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes
inferred← citeshttps://doi.org/10.1002/mgg3.2226openalex-snapshot
Genome‐wide meta‐analyses identify five new risk loci for nonsyndromic orofacial clefts in the Chinese Han population
inferred← citeshttps://doi.org/10.1002/mgg3.273openalex-snapshot
The prevalence, penetrance, and expressivity of etiologic IRF 6variants in orofacial clefts patients from sub‐Saharan Africa
inferred← citeshttps://doi.org/10.1002/mgg3.459openalex-snapshot
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts
inferred← citeshttps://doi.org/10.1002/mgg3.497openalex-snapshot
Associations of genetic variants in endocytic trafficking of epidermal growth factor receptor super pathway with risk of nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/mgg3.53openalex-snapshot
Analysis of PRICKLE 1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations
inferred← citeshttps://doi.org/10.1002/mgg3.714openalex-snapshot
Three GLI2 mutations combined potentially underlie non‐syndromic cleft lip with or without cleft palate in a Chinese pedigree
inferred← citeshttps://doi.org/10.1002/mgg3.918openalex-snapshot
Interleukin 10 gene polymorphisms and frailty syndrome in elderly Mexican people: (Sadem study)
inferred← citeshttps://doi.org/10.1002/osi2.1072openalex-snapshot
Gene–environment interplay and MicroRNAs in cleft lip and cleft palate
inferred← citeshttps://doi.org/10.1002/osi2.1132openalex-snapshot
Clinical and socioenvironmental characterizations associated with the genealogical analysis of a group of Dominican patients with nonsyndromic cleft lip with or without cleft palate
inferred← citeshttps://doi.org/10.1002/pd.5499openalex-snapshot
Accurate diagnosis of fetal cleft lip/palate by typical signs of magnetic resonance imaging
inferred← citeshttps://doi.org/10.1002/pdi3.70037openalex-snapshot
A Comprehensive Review of the Genetic Etiology and Management of Orofacial Clefts
inferred← citeshttps://doi.org/10.1002/tkm2.1422openalex-snapshot
Sasa veitchii extract alleviates phenobarbital‐induced cell proliferation inhibition by upregulating transforming growth factor‐beta 1
inferred← citeshttps://doi.org/10.1002/wdev.336openalex-snapshot
Choanal atresia and stenosis: Development and diseases of the nasal cavity
inferred← citeshttps://doi.org/10.1002/wsbm.1265openalex-snapshot
Signaling networks in palate development
inferred← citeshttps://doi.org/10.1007/978-1-0716-1847-9_5openalex-snapshot
Methodology for Free-Floating Organ Culture of Mid-gestation Maxillary Primordial Tissue
inferred← citeshttps://doi.org/10.1007/978-1-0716-1847-9_6openalex-snapshot
Methods of Palate Culture in Later Palatogenesis: Elevation, Horizontal Outgrowth, and Fusion
inferred← citeshttps://doi.org/10.1007/978-1-0716-2613-9_3openalex-snapshot
Teleost Fish as Model Animals to Understand Alcohol Teratology
inferred← citeshttps://doi.org/10.1007/978-1-4614-1683-8_6openalex-snapshot
Regulatory Mutations Leading to Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1007/978-3-030-25905-1_17openalex-snapshot
Genetic Causes of Female Infertility
inferred← citeshttps://doi.org/10.1007/978-3-030-50123-5_9openalex-snapshot
Epidemiology of Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1007/978-3-030-59105-2_2openalex-snapshot
Burden of Cleft Disease and Opportunity for Impact
inferred← citeshttps://doi.org/10.1007/978-3-031-21317-5_22openalex-snapshot
Malformations and Malformative Syndromes Associated with CDH1
inferred← citeshttps://doi.org/10.1007/978-3-031-24636-4_2openalex-snapshot
Clinical and Diagnostic Anatomy
inferred← citeshttps://doi.org/10.1007/978-3-031-26098-8_5openalex-snapshot
The Neural Crest and Craniofacial Malformations
inferred← citeshttps://doi.org/10.1007/978-3-031-28069-6_7openalex-snapshot
Treatment Principles in Orofacial Clefts
inferred← citeshttps://doi.org/10.1007/978-3-031-28069-6_8openalex-snapshot
Diagnosis and Classification of Branchial Arch Diseases
inferred← citeshttps://doi.org/10.1007/978-3-031-36593-5_28openalex-snapshot
Excision of Palatal Neoplasms
inferred← citeshttps://doi.org/10.1007/978-3-031-36962-9_210-2openalex-snapshot
Introduction to Cleft Lip and Palate
inferred← citeshttps://doi.org/10.1007/978-3-031-84663-2_31openalex-snapshot
Interdisciplinary Team Care
inferred← citeshttps://doi.org/10.1007/978-3-031-96947-8_10openalex-snapshot
Fetal Surgery for Cleft Lip and Palate: Rationale and Evidence
inferred← citeshttps://doi.org/10.1007/978-3-031-96947-8_21openalex-snapshot
Atypical Facial Cleft Detected by Prenatal Scan and Confirmed by Postmortem Reconstructive Computed Tomography (CT REC)
inferred← citeshttps://doi.org/10.1007/978-3-319-08599-9_43openalex-snapshot
Results from Using Automatic Speech Recognition in Cleft Speech Therapy with Children
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