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Lista de obras de Mary L. Marazita

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis

artículo científico publicado en 2006

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.

artículo científico publicado en 2017

A genome wide linkage scan for cleft lip and palate and dental anomalies

article published in 2008

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

artículo científico publicado en 2014

A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts

artículo científico publicado en 2015

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1

artículo científico publicado en 2002

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

artículo científico publicado en 2019

Aggressive periodontitis is likely influenced by a few small effect genes

artículo científico publicado en 2009

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

scientific article published on 09 December 2011

An ordered subset approach to including covariates in the transmission disequilibrium test

artículo científico publicado en 2007

Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.

artículo científico publicado en 2013

Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families.

artículo científico publicado en 2017

Anatomical basis for apparent subepithelial cleft lip: a histological and ultrasonographic survey of the orbicularis oris muscle

scientific article published on 14 December 2007

Anthropometric precision and accuracy of digital three-dimensional photogrammetry: comparing the Genex and 3dMD imaging systems with one another and with direct anthropometry

artículo científico publicado en 2006

Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries

artículo científico publicado en 2015

Asian oral-facial cleft birth prevalence

artículo científico publicado en 2006

Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts

artículo científico publicado en 2018

Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight.

artículo científico publicado en 2013

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis

artículo científico publicado en 2003

Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies

artículo científico publicado en 2013

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2017

Bilateral Asymmetry in Chinese Families with Cleft Lip with or without Cleft Palate

artículo científico publicado en 2005

CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2010

Candidate gene linkage approach to identify DNA variants that predispose to preterm birth

artículo científico publicado en 2012

Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts

artículo científico publicado en 2008

Candidate genes for oral-facial clefts in Guatemalan families.

artículo científico publicado en 2006

Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia

artículo científico publicado en 2015

Caries: review of human genetics research

artículo científico publicado en 2014

Characterization of dermatoglyphics in PHOX2B-confirmed congenital central hypoventilation syndrome.

artículo científico publicado en 2006

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Chromosome 17: gene mapping studies of cleft lip with or without cleft palate in Chinese families

artículo científico publicado en 2003

Cleft Palate-Craniofacial Journal 50th anniversary editorial board commentary: anatomy, basic sciences, and genetics--then and now.

artículo científico publicado en 2014

Cleft lip and palate: understanding genetic and environmental influences ⬇️

artículo científico publicado el 1 de marzo de 2011

Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian-randomization study

scientific article published on 06 May 2020

Co-occurrence of yeast, streptococci, dental decay, and gingivitis in the post-partum period: results of a longitudinal study

artículo científico publicado en 2020

Collecting psychosocial self-report data in oral health research: impact of literacy level and computerised administration.

artículo científico publicado en 2013

Comparative microanatomy of the orbicularis oris muscle between chimpanzees and humans: evolutionary divergence of lip function

artículo científico publicado en 2009

Congenital Central Hypoventilation Syndrome

artículo científico publicado en 2014

Consortium genome-wide meta-analysis for childhood dental caries traits

Consortium-based genome-wide meta-analysis for childhood dental caries traits

scholarly article by Simon Haworth published in September 2018

Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay

scientific article published on 24 June 2019

Cryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization

artículo científico publicado en 2009

Current concepts in the embryology and genetics of cleft lip and cleft palate

artículo científico publicado en 2004

Demographic and prenatal factors of patients with cleft lip and cleft palate. A pilot study

artículo científico publicado en 2003

Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses

artículo científico publicado en 2012

Depression and Rural Environment are Associated With Poor Oral Health Among Pregnant Women in Northern Appalachia.

artículo científico publicado en 2015

Dermatoglyphic Pattern Types in Subjects with Nonsyndromic Cleft Lip with or without Cleft Palate (CL/P) and Their Unaffected Relatives in the Philippines

scholarly article by Nicole M. Scott et al published July 2005 in Cleft Palate: Craniofacial Journal

Dermatoglyphic fingerprint heterogeneity among individuals with nonsyndromic cleft lip with or without cleft palate and their unaffected relatives in China and the Philippines

scientific article published on 01 April 2005

Detectable clonal mosaicism from birth to old age and its relationship to cancer

artículo científico publicado en 2012

Detection of Streptococcus mutans Genomic DNA in Human DNA Samples Extracted from Saliva and Blood

artículo científico publicado en 2011

Detection of de novo copy number deletions from targeted sequencing of trios

artículo científico publicado en 2019

Determination of genetic predisposition to patent ductus arteriosus in preterm infants

artículo científico publicado en 2009

Diagnosing subtle palatal anomalies: Validation of video-analysis and assessment protocol for diagnosing occult submucous cleft palate.

artículo científico publicado en 2017

Digital three-dimensional photogrammetry: evaluation of anthropometric precision and accuracy using a Genex 3D camera system.

artículo científico publicado en 2004

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

artículo científico publicado en 2008

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis

artículo científico publicado en 2002

Ear Infection in Isolated Cleft Lip: Etiological Implications.

artículo científico publicado en 2015

Effects of Specimen Collection Methodologies and Storage Conditions on the Short-Term Stability of Oral Microbiome Taxonomy

artículo científico publicado en 2016

Effects of enamel matrix genes on dental caries are moderated by fluoride exposures

artículo científico publicado en 2014

Effects of smoking and genotype on the PSR index of periodontal disease in adults aged 18-49.

artículo científico publicado en 2012

Enamel formation genes influence enamel microhardness before and after cariogenic challenge.

artículo científico publicado en 2012

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

artículo científico publicado en 2010

Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth

artículo científico publicado en 2007

Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.

artículo científico publicado en 2016

Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate

artículo científico publicado en 2011

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate

artículo científico publicado en 2012

Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate

artículo científico publicado en 2014

Evidence of olfactory deficits as part of the phenotypic spectrum of nonsyndromic orofacial clefting

artículo científico publicado en 2015

Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans

artículo científico publicado en 2012

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

artículo científico publicado en 2020

Exploration of genetic factors determining cleft side in a pair of monozygotic twins with mirror-image cleft lip and palate using whole-genome sequencing and comparison of craniofacial morphology

scientific article published on 19 August 2018

Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.

artículo científico publicado en 2014

Exploring Subclinical Phenotypic Features in Twin Pairs Discordant for Cleft Lip and Palate

scientific article published on 16 February 2016

Exploring the effect of dentition, dental decay and familiality on oral health using metabolomics.

artículo científico publicado en 2013

Exploring the genomic basis of early childhood caries: a pilot study

artículo científico publicado en 2017

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.

artículo científico publicado en 2012

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

artículo científico publicado en 2009

FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research

scientific article published on 21 September 2020

Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology

artículo científico publicado en 2005

Facial recognition from DNA using face-to-DNA classifiers

scientific article published on 11 June 2019

Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate.

artículo científico publicado en 2010

GWAS reveals loci associated with velopharyngeal dysfunction.

artículo científico publicado en 2018

Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios

artículo científico publicado en 2015

Gene-environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop

artículo científico publicado en 2011

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.

artículo científico publicado en 2017

Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits

artículo científico publicado en 2016

Genetic Modifiers of Patent Ductus Arteriosus in Term Infants

artículo científico publicado en 2016

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

article

Genetic association and differential expression of PITX2 with acute appendicitis

artículo científico publicado en 2018

Genetic contributions to the development of retinopathy of prematurity

artículo científico publicado en 2009

Genetic correlation between smoking behaviors and schizophrenia

artículo científico publicado en 2017

Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities

artículo científico publicado en 2016

Genetic mapping of high caries experience on human chromosome 13.

artículo científico publicado en 2013

Genetic susceptibility to dental caries differs between the sexes: a family-based study.

artículo científico publicado en 2015

Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.

artículo científico publicado en 2018

Genetics of cleft lip and cleft palate.

artículo científico publicado en 2013

Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families

artículo científico publicado en 2002

Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India

scientific article published on 01 October 2004

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

scientific article published on 11 June 2009

Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations

artículo científico publicado en 2021

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

artículo científico publicado en 2012

Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study

scientific article published on 27 September 2019

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

artículo científico publicado en 2016

Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey

artículo científico publicado en 2004

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

artículo científico publicado en 2020

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity

artículo científico publicado en 2017

Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course

artículo científico publicado en 2013

Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.

artículo científico publicado en 2019

Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios.

artículo científico publicado en 2017

Genome-wide association scan of dental caries in the permanent dentition

artículo científico publicado en 2012

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate

artículo científico publicado en 2015

Genome-wide association study identifies four loci associated with eruption of permanent teeth

artículo científico publicado en 2011

Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL)

artículo científico publicado en 2015

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

artículo científico publicado en 2017

Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years

artículo científico publicado en 2014

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

artículo científico publicado en 2018

Genome-wide mapping of global-to-local genetic effects on human facial shape.

artículo científico publicado en 2018

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

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

artículo científico publicado en 2017

Genomic analyses in African populations identify novel risk loci for cleft palate

scientific article published on 01 March 2019

Hair whorls and handedness: informative phenotypic markers in nonsyndromic cleft lip with or without cleft palate (NS CL/P) cases and their unaffected relatives

artículo científico publicado en 2005

Heritability of Face Shape in Twins: A Preliminary Study using 3D Stereophotogrammetry and Geometric Morphometrics.

artículo científico publicado en 2013

Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses

artículo científico publicado en 2012

Human telomere length correlates to the size of the associated chromosome arm.

artículo científico publicado en 2009

Hypertelorism and Orofacial Clefting Revisited: An Anthropometric Investigation

scientific article published on 09 August 2016

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

artículo científico publicado en 2017

Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts

artículo científico publicado en 2018

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

artículo científico publicado en 2017

Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations

artículo científico publicado en 2005

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b ⬇️

artículo científico publicado el 15 de diciembre de 2003

Impaired FGF signaling contributes to cleft lip and palate

artículo científico publicado en 2007

In a Vietnamese population, MSX1 variants contribute to cleft lip and palate

artículo científico publicado en 2004

In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome

artículo científico publicado en 2005

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

article

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants

article

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives

artículo científico publicado en 2014

Insights into the genetic architecture of the human face

artículo científico publicado en 2020

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

artículo científico publicado en 2012

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

artículo científico publicado en 2004

Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America

scientific article published on 01 September 2007

Intraobserver error associated with measurements of the hand.

artículo científico publicado en 2005

Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology

artículo científico publicado en 2018

Is the Fagerström test for nicotine dependence invariant across secular trends in smoking? A question for cross-birth cohort analysis of nicotine dependence.

artículo científico publicado en 2018

Low levels of salivary metals, oral microbiome composition and dental decay

scientific article published on 04 September 2020

Mapping genetic variants for cranial vault shape in humans.

artículo científico publicado en 2018

Maternal serum 25-hydroxyvitamin D concentrations are associated with small-for-gestational age births in white women

artículo científico publicado en 2010

Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challenges

artículo científico publicado en 2012

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

artículo científico publicado en 2005

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

artículo científico publicado en 2004

Methods for detecting gene x gene interaction in multiplex extended pedigrees

artículo científico publicado en 2005

Minor physical anomalies in schizophrenia: a meta-analysis

scientific article published on 31 October 2006

Multi-dimensional prioritization of dental caries candidate genes and its enriched dense network modules

artículo científico publicado en 2013

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment

artículo científico publicado en 2017

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

artículo científico publicado en 2009

Nasolabial fold discontinuity during speech as a possible extended cleft phenotype

artículo científico publicado en 2012

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome

artículo científico publicado en 2006

No observed association for mitochondrial SNPs with preterm delivery and related outcomes

artículo científico publicado en 2012

Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome

scientific article published on 17 June 2020

Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions

artículo científico publicado en 2002

Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.

artículo científico publicado en 2018

Novel caries loci in children and adults implicated by genome-wide analysis of families.

artículo científico publicado en 2018

Novel genetic loci affecting facial shape variation in humans

artículo científico publicado en 2019

Oral Health in a Sample of Pregnant Women from Northern Appalachia (2011-2015)

artículo científico publicado en 2015

Oral health and related risk indicators in north-central Appalachia differ by rurality

artículo científico publicado en 2020

Oral health disparities in Appalachia: orthodontic treatment need and demand

artículo científico publicado en 2008

Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate

scientific article published on 01 June 2007

Parental evaluation of informing interviews for cleft lip and/or palate

artículo científico publicado en 2003

Parents of Children With Nonsyndromic Orofacial Clefting Show Altered Palate Shape

artículo científico publicado en 2020

Perceived social support of mothers of children with clefts

artículo científico publicado en 2003

Periodontal Status and Quality of Life: Impact of Fear of Pain and Dental Fear.

artículo científico publicado en 2017

Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience

artículo científico publicado en 2011

Pittsburgh Registry of Infant Multiplets (PRIM).

artículo científico publicado en 2002

Pittsburgh Registry of Infant Multiplets (PRIM): an update

artículo científico publicado en 2006

Predictors of dental care utilization in north-central Appalachia in the USA

artículo científico publicado en 2019

Prevalence 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 syndrome

artículo científico publicado en 2009

Prevalence of Torus Palatinus and association with dental arch shape in a multi-ethnic cohort

artículo científico publicado en 2020

Primary teeth microhardness and lead (Pb) levels

Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation

artículo científico publicado en 2011

Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.

artículo científico publicado en 2014

Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.

artículo científico publicado en 2015

Replication of a genome-wide association study of birth weight in preterm neonates

artículo científico publicado en 2011

Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).

artículo científico publicado en 2013

Reply to Hook

Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases

artículo científico publicado en 2008

Role of TRAV locus in low caries experience

artículo científico publicado en 2013

Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay

artículo científico publicado en 2014

Role of polymorphic variants as genetic modulators of infection in neonatal sepsis

artículo científico publicado en 2010

SNPs Associated With Testosterone Levels Influence Human Facial Morphology

scholarly article by Jasmien Roosenboom et al published 2018 in Frontiers in Genetics

Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.

artículo científico publicado en 2013

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

artículo científico publicado en 2013

Single-Nucleotide Polymorphisms in the KCNN3 Gene Associate With Preterm Birth ⬇️

artículo científico publicado el 25 de enero de 2011

Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation

scientific article published on 25 October 2018

Soft tissue nasal asymmetry as an indicator of orofacial cleft predisposition

artículo científico publicado en 2018

Sonic hedgehog regulation of Foxf2 promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis.

artículo científico publicado en 2017

Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects

artículo científico publicado en 2005

Study protocol of the Center for Oral Health Research in Appalachia (COHRA) etiology study

artículo científico publicado en 2008

Sudden Infant Death Syndrome: review of implicated genetic factors

artículo científico publicado en 2007

Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).

artículo científico publicado en 2008

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

scientific article published on 01 August 2006

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene

scientific article published on 01 March 2003

Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development

artículo científico publicado en 2004

Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting

scientific article published on 08 September 2017

The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community

artículo científico publicado en 2015

The FaceBase Consortium: a comprehensive program to facilitate craniofacial research

artículo científico publicado en 2011

The FaceBase Consortium: a comprehensive resource for craniofacial researchers

artículo científico publicado en 2016

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

artículo científico publicado en 2010

The Human Phenotype Ontology in 2024: phenotypes around the world

artículo científico publicado en 2023

The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P

artículo científico publicado en 2009

The PhenX Toolkit: get the most from your measures

artículo científico publicado en 2011

The Pittsburgh Fistula Classification System: a standardized scheme for the description of palatal fistulas

artículo científico publicado en 2007

The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification.

artículo científico publicado en 2006

The effects of family, dentition, and dental caries on the salivary microbiome.

artículo científico publicado en 2016

The use of ultrasound to visualize the upper lips of noncleft and repaired-cleft individuals

artículo científico publicado en 2007

Third molar agenesis as a potential marker for craniofacial deformities.

artículo científico publicado en 2018

Three-dimensional assessment of the pharyngeal airway in Japanese preschoolers with orofacial clefts

artículo científico publicado en 2019

Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: a possible marker for genetic susceptibility

artículo científico publicado en 2008

Toward a genetic understanding of dental fear: evidence of heritability

artículo científico publicado en 2016

Transmission analysis of candidate genes for nonsyndromic oral clefts in Brazilian parent-child triads with recurrence

article

Transmission of dental fear from parent to adolescent in an Appalachian sample in the USA

scientific article published on 12 September 2019

Use of 16S ribosomal RNA gene analyses to characterize the bacterial signature associated with poor oral health in West Virginia

artículo científico publicado en 2011

Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies

artículo científico publicado en 2012

Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium

artículo científico publicado en 2015

Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adults

artículo científico publicado en 2016

Using the PhenX Toolkit to Add Standard Measures to a Study

article

Vaginal and oral microbes, host genotype and preterm birth

artículo científico publicado en 2009

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

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Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries

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Vitamin D metabolic loci and preeclampsia risk in multi-ethnic pregnant women

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Vitamin D metabolic loci and vitamin D status in Black and White pregnant women

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Whole exome association of rare deletions in multiplex oral cleft families

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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

artículo científico publicado en 2014

Whole-genome sequencing in a pair of monozygotic twins with discordant cleft lip and palate subtypes

artículo científico publicado en 2018

Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Women are more susceptible to caries but individuals born with clefts are not.

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X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.

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X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts

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