Mary L. Marazita
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American geneticist
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Why Is Mary L. Marazita Influential?
(Suggest an Edit or Addition)According to Wikipedia, Mary Louise Marazita is an American geneticist. She is a Distinguished Professor at the University of Pittsburgh School of Dental Medicine. Early life and education Marazita was born in Cheboygan, Michigan to parents Philip and Eleanor Marazita. She graduated with her bachelor's degree in animal husbandry from Michigan State University and her PhD in genetics from the University of North Carolina at Chapel Hill. She wrote her thesis under the guidance of Robert C. Elston. Following her PhD, Marazita completed her post-doctoral training in craniofacial biology at the University of Southern California from 1980 to 1982.
Mary L. Marazita's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Cleft lip and palate: understanding genetic and environmental influences (2011) (1397)
- Genome-wide Association Studies (2012) (1122)
- Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. (2004) (568)
- The PhenX Toolkit: Get the Most From Your Measures (2011) (520)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer (2012) (514)
- A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 (2010) (503)
- Genetic epidemiological studies of early-onset deafness in the U.S. school-age population. (1993) (472)
- Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b (2003) (363)
- Disruption of an AP-2α binding site in an IRF6 enhancer is strongly associated with cleft lip (2008) (355)
- Anthropometric Precision and Accuracy of Digital Three-Dimensional Photogrammetry: Comparing the Genex and 3dMD Imaging Systems with One Another and with Direct Anthropometry (2006) (324)
- Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci (2012) (316)
- Maternal serum 25-hydroxyvitamin D concentrations are associated with small-for-gestational age births in white women. (2010) (300)
- Impaired FGF signaling contributes to cleft lip and palate (2007) (275)
- Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate (2005) (250)
- Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis (2002) (241)
- Digital Three-Dimensional Photogrammetry: Evaluation of Anthropometric Precision and Accuracy Using a Genex 3D Camera System (2004) (227)
- Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. (2004) (218)
- Evidence for autosomal dominant inheritance and race-specific heterogeneity in early-onset periodontitis. (1994) (214)
- Genome‐wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early‐onset, major depression (2003) (201)
- Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. (2009) (189)
- A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. (2002) (189)
- Genetics of cleft lip and cleft palate (2013) (174)
- Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity (2017) (174)
- The evolution of human genetic studies of cleft lip and cleft palate. (2012) (174)
- The Pittsburgh Fistula Classification System: A Standardized Scheme for the Description of Palatal Fistulas (2007) (172)
- Asian Oral-Facial Cleft Birth Prevalence (2006) (169)
- The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions (2010) (161)
- Genome-wide mapping of global-to-local genetic effects on human facial shape (2018) (157)
- Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate (2011) (156)
- Enamel Formation Genes Are Associated with High Caries Experience in Turkish Children (2008) (155)
- 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. (2016) (154)
- Possible Association of Amelogenin to High Caries Experience in a Guatemalan-Mayan Population (2007) (144)
- FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. (2009) (143)
- A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling. (2004) (140)
- 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. (2015) (139)
- Genome-wide Scan Finds Suggestive Caries Loci (2008) (138)
- Taste Genes Associated with Dental Caries (2010) (137)
- Sudden Infant Death Syndrome: Review of implicated genetic factors (2007) (136)
- Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study (2013) (133)
- Genetic factors influencing risk to orofacial clefts: today’s challenges and tomorrow’s opportunities (2016) (132)
- Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene (2003) (132)
- Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology (2016) (132)
- 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 (2009) (129)
- Current concepts in the embryology and genetics of cleft lip and cleft palate. (2004) (127)
- A specific requirement for PDGF-C in palate formation and PDGFR-α signaling (2004) (126)
- Caries: Review of Human Genetics Research (2014) (126)
- Genes and Their Effects on Dental Caries May Differ between Primary and Permanent Dentitions (2010) (124)
- Tuftelin, Mutans Streptococci, and Dental Caries Susceptibility (2005) (124)
- MSX1 and TGFB3 Contribute to Clefting in South America (2003) (123)
- Descriptive epidemiology of nonsyndromic cleft lip with or without cleft palate in Shanghai, China, from 1980 to 1989. (2000) (123)
- Minor physical anomalies in schizophrenia: A meta-analysis (2007) (120)
- Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. (2013) (120)
- Intraobserver error associated with measurements of the hand (2005) (117)
- A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4 (2010) (115)
- Genome-wide Association Scan for Childhood Caries Implicates Novel Genes (2011) (115)
- Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression. (2002) (115)
- Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism. (1985) (114)
- Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation (2000) (113)
- 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 (2009) (113)
- Association of the serotonin transporter gene with sudden infant death syndrome: A haplotype analysis (2003) (112)
- 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 (2017) (111)
- Face shape of unaffected parents with cleft affected offspring: combining three-dimensional surface imaging and geometric morphometrics. (2009) (109)
- A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. (2016) (109)
- In a Vietnamese population, MSX1 variants contribute to cleft lip and palate (2004) (108)
- The Pittsburgh Oral-Facial Cleft Study: Expanding the Cleft Phenotype. Background and Justification (2006) (107)
- Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. (2002) (105)
- Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data (2019) (104)
- Evidence of Genetic Heterogeneity for Hereditary Gingival Fibromatosis (2000) (103)
- Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic Development (2004) (100)
- Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence (2017) (100)
- Gene‐environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop (2011) (99)
- A Qualitative Description of Receiving a Diagnosis of Clefting in the Prenatal or Postnatal Period (2008) (96)
- Sequence variations in CREB1 cosegregate with depressive disorders in women (2003) (94)
- Genetic and Environmental Factors Associated with Dental Caries in Children: The Iowa Fluoride Study (2012) (93)
- Enamel Formation Genes Influence Enamel Microhardness Before and After Cariogenic Challenge (2012) (92)
- Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts (2008) (91)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome. (2001) (89)
- Role of Polymorphic Variants as Genetic Modulators of Infection in Neonatal Sepsis (2010) (88)
- 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. (2012) (88)
- Study protocol of the Center for Oral Health Research in Appalachia (COHRA) etiology study (2008) (86)
- Gene mapping studies with the syndrome of autism (1985) (85)
- Congenital central hypoventilation syndrome: inheritance and relation to sudden infant death syndrome. (1993) (82)
- Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate (2007) (81)
- Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
- Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate (2015) (80)
- Genetic analysis of cleft lip with or without cleft palate in Chinese kindreds. (1984) (79)
- AXIS inhibition protein 2, orofacial clefts and a family history of cancer. (2009) (79)
- Genome-wide association Scan of dental caries in the permanent dentition (2012) (78)
- Candidate gene and locus analysis of myopia (2007) (76)
- Segregation Analysis of Mandibular Prognathism in Libya (2003) (76)
- GWAS of Dental Caries Patterns in the Permanent Dentition (2013) (75)
- Re-interpretation of the evidence for X-linked dominant inheritance of juvenile periodontitis. (1992) (75)
- The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. (2011) (75)
- Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus. (1992) (74)
- Genome‐wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early‐onset, major depression (2004) (74)
- Further evidence of a relationship between the retinoic acid receptor alpha locus and nonsyndromic cleft lip with or without cleft palate (CL +/- P) (1993) (72)
- Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery (2007) (71)
- The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community (2016) (71)
- Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2 (2017) (68)
- No female preponderance in juvenile periodontitis after correction for ascertainment bias. (1991) (68)
- Facial Phenotype in Children and Young Adults with PHOX2B–Determined Congenital Central Hypoventilation Syndrome: Quantitative Pattern of Dysmorphology (2006) (67)
- Whole Exome Sequencing of Distant Relatives in Multiplex Families Implicates Rare Variants in Candidate Genes for Oral Clefts (2014) (67)
- Parental evaluation of informing interviews for cleft lip and/or palate. (2003) (67)
- In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome (2005) (66)
- Determination of Genetic Predisposition to Patent Ductus Arteriosus in Preterm Infants (2009) (65)
- Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families (2004) (65)
- Contributions of PTCH Gene Variants to Isolated Cleft Lip and Palate (2006) (65)
- Genetic Contributions to the Development of Retinopathy of Prematurity (2009) (64)
- Evaluation of Fetal and Maternal Genetic Variation in the Progesterone Receptor Gene for Contributions to Preterm Birth (2007) (64)
- Genetic correlation between smoking behaviors and schizophrenia (2017) (64)
- Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adults (2016) (63)
- 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) (2013) (62)
- Segregation analysis of attention deficit hyperactivity disorder. (1999) (62)
- A genome wide linkage scan for cleft lip and palate and dental anomalies (2008) (62)
- Genetic analysis of candidate loci in non‐syndromic cleft lip families from Antioquia‐Colombia and Ohio (2004) (62)
- Vitamin D receptor (VDR) and group-specific component (GC, vitamin D-binding protein) polymorphisms in myopia. (2011) (61)
- Genetic Susceptibility to Dental Caries Differs between the Sexes: A Family-Based Study (2015) (60)
- Insights into the genetic architecture of the human face (2020) (58)
- Genome-wide Association Studies of Pit-and-Fissure- and Smooth-surface Caries in Permanent Dentition (2013) (57)
- 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. (2007) (57)
- Nonsyndromic cleft lip with or without cleft palate in west Bengal, India: evidence for an autosomal major locus. (1993) (57)
- Genome-Wide Association Study of Periodontal Health Measured by Probing Depth in Adults Ages 18−49 years (2013) (56)
- Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 (2010) (56)
- Social anxiety in Chinese adults with oral-facial clefts. (2001) (56)
- Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England (1986) (55)
- The FaceBase Consortium: a comprehensive resource for craniofacial researchers (2016) (55)
- Phenotype harmonization and cross‐study collaboration in GWAS consortia: the GENEVA experience (2011) (55)
- A genome‐wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11‐23 (2007) (54)
- Genetic Susceptibility to Dental Caries on Pit and Fissure and Smooth Surfaces (2012) (54)
- Genetic loci for pathological myopia are not associated with juvenile myopia. (2002) (54)
- Studies of reduced folate carrier 1 (RFC1) A80G and 5,10‐methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects (2005) (54)
- Three‐dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility (2008) (54)
- Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits (2020) (53)
- Vaginal and oral microbes, host genotype and preterm birth. (2009) (52)
- The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P (2009) (52)
- Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome. (2001) (50)
- Parental craniofacial morphology in cleft lip with or without cleft palate as determined by cephalometry: a meta-analysis. (2006) (50)
- Sonic hedgehog regulation of Foxf2 promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis (2017) (50)
- Major gene determination of liability to cleft lip with or without cleft palate: a multiracial view. (1986) (49)
- Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate (2012) (48)
- Novel genetic loci affecting facial shape variation in humans (2019) (46)
- The impact of molecular genetics on oral health paradigms. (2000) (46)
- Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia (2015) (45)
- Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting (2017) (45)
- Genetic analysis of cleft lip with or without cleft palate in Madras, India. (1992) (45)
- Spectrum of Dental Phenotypes in Nonsyndromic Orofacial Clefting (2015) (45)
- Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos (2017) (45)
- Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations (2016) (44)
- Genetic segregation analysis of early-onset recurrent unipolar depression. (1997) (44)
- Interferon regulatory factor 6 (IRF6) is associated with oral‐facial cleft in individuals that originate in South America (2007) (44)
- 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. (2015) (44)
- Rethinking isolated cleft palate: Evidence of occult lip defects in a subset of cases (2008) (44)
- IRF6 mutation screening in non‐syndromic orofacial clefting: analysis of 1521 families (2016) (43)
- Reevaluation of the chromosome 4q candidate region for early onset periodontitis (1993) (43)
- Genomic analyses in African populations identify novel risk loci for cleft palate (2018) (43)
- Heritability of Face Shape in Twins: A Preliminary Study using 3D Stereophotogrammetry and Geometric Morphometrics. (2013) (43)
- Genome‐scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey (2004) (42)
- Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study (2013) (42)
- Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population. (2002) (41)
- Hair keratin mutations in tooth enamel increase dental decay risk. (2014) (41)
- Epidemiological and genetic study of 121 cases of oral clefts in Kuwait. (2002) (40)
- Social Anxiety in Chinese Adults with Oral-Facial Clefts (2001) (40)
- Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 (2012) (40)
- Facial recognition from DNA using face-to-DNA classifiers (2019) (40)
- Genome wide study of maternal and parent‐of‐origin effects on the etiology of orofacial clefts (2012) (40)
- Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions. (2002) (40)
- Genetic analysis of cleft lip with or without cleft palate in Danish kindreds. (1984) (39)
- Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate (2009) (39)
- Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration (2018) (39)
- Exploratory genotype–phenotype correlations of facial form and asymmetry in unaffected relatives of children with non‐syndromic cleft lip and/or palate (2014) (39)
- Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth (2011) (38)
- Association of AXIN2 with Non-syndromic Oral Clefts in Multiple Populations (2012) (38)
- A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. I. Segregation analysis. (1987) (38)
- The autosomal dominant form of “pure” familial spastic paraplegia (1987) (37)
- Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challenges. (2012) (37)
- Genetic segregation analyses of serum IgG2 levels. (1996) (37)
- FOXE 1 association with both isolated cleft lip with or without cleft palate , and isolated cleft palate (2009) (37)
- Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India (2004) (36)
- Rapid Testing of SNPs and Gene–Environment Interactions in Case–Parent Trio Data Based on Exact Analytic Parameter Estimation (2012) (36)
- Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay (2014) (35)
- Fine-Mapping of 5q12.1–13.3 Unveils New Genetic Contributors to Caries (2013) (35)
- Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology (2018) (34)
- Follow‐up association studies of chromosome region 9q and nonsyndromic cleft lip/palate (2010) (34)
- Comparative microanatomy of the orbicularis oris muscle between chimpanzees and humans: evolutionary divergence of lip function (2009) (34)
- Aggressive periodontitis is likely influenced by a few small effect genes. (2009) (34)
- Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses (2012) (34)
- Edinburgh Research Explorer Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip (2018) (33)
- Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase‐activating polypeptide (PACAP) (2009) (33)
- Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking (2013) (33)
- Effects of enamel matrix genes on dental caries are moderated by fluoride exposures (2015) (33)
- Prenatal sex hormones, digit ratio, and face shape in adult males. (2015) (33)
- Oral Health in a Sample of Pregnant Women from Northern Appalachia (2011–2015) (2015) (32)
- Rare and Common Variants Conferring Risk of Tooth Agenesis (2018) (32)
- Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. (2020) (31)
- Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment (2017) (31)
- Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. (2012) (31)
- Genetic linkage studies in Alzheimer's disease (1986) (31)
- Evidence of Gene−Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate (2014) (31)
- CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip with or without Cleft Palate (2011) (30)
- Consortium-based genome-wide meta-analysis for childhood dental caries traits (2018) (30)
- Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses. (2013) (30)
- Innovative approach to genetic counseling services for the deaf population. (1992) (30)
- Genome-Wide Association Study of Primary Dentition Pit-and-Fissure and Smooth Surface Caries (2014) (30)
- Demographic and prenatal factors of patients with cleft lip and cleft palate. A pilot study. (2003) (30)
- Evidence for a major gene in familial anencephaly. (1990) (30)
- Genetic segregation analysis of recurrent, early-onset major depression: evidence for single major locus transmission. (2002) (30)
- Anatomical Basis for Apparent Subepithelial Cleft Lip: A Histological and Ultrasonographic Survey of the Orbicularis Oris Muscle (2008) (29)
- Use of 16S ribosomal RNA gene analyses to characterize the bacterial signature associated with poor oral health in West Virginia (2011) (29)
- Sudden infant death syndrome: Case‐control frequency differences in paired like homeobox (PHOX) 2B gene (2006) (29)
- Rare functional variants in genome–wide association identified candidate genes for nonsyndromic clefts in the African population (2014) (29)
- GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos (2017) (29)
- Candidate Genes for Oral-Facial Clefts in Guatemalan Families (2006) (29)
- Nonsyndromic Cleft Lip with or without Cleft Palate in China: Assessment of Candidate Regions (2002) (28)
- Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL). (2016) (28)
- Analysis of variability of clinical manifestations in Waardenburg syndrome. (1995) (28)
- Oral health disparities in Appalachia: orthodontic treatment need and demand. (2008) (28)
- Genetic Etiologies of Facial Clefting (2003) (28)
- Association studies of low‐frequency coding variants in nonsyndromic cleft lip with or without cleft palate (2017) (28)
- Segregation analysis of alcoholism in high density families: a replication. (1996) (28)
- Candidate gene linkage approach to Identify DNA variants that predispose to preterm birth (2012) (27)
- Association between non-right-handedness and cleft lip with or without cleft palate in a Chinese population. (1997) (27)
- Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between Asians and Europeans (2012) (27)
- Gene‐Gene Interaction Among WNT Genes for Oral Cleft in Trios (2015) (27)
- Effects of Specimen Collection Methodologies and Storage Conditions on the Short-Term Stability of Oral Microbiome Taxonomy (2016) (27)
- Replication of a genome-wide association study of birth weight in preterm neonates. (2012) (27)
- Transforming Growth Factor Alpha: A Modifying Locus for Nonsyndromic Cleft Lip with or without Cleft Palate? (1994) (26)
- Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans (2015) (26)
- Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives (2014) (26)
- Dermatoglyphic Pattern Types in Subjects with Nonsyndromic Cleft Lip with or without Cleft Palate (CL/P) and Their Unaffected Relatives in the Philippines (2005) (26)
- No Observed Association for Mitochondrial SNPs with Preterm Delivery and Related Outcomes (2012) (26)
- Depression and Rural Environment Are Associated With Poor Oral Health Among Pregnant Women in Northern Appalachia (2016) (25)
- Periodontal Status and Quality of Life: Impact of Fear of Pain and Dental Fear (2017) (25)
- Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome (2006) (25)
- Clustering Tooth Surfaces into Biologically Informative Caries Outcomes (2013) (25)
- Comparative whole-genome analysis of Streptococcus mutans isolates within and among individuals of different caries status. (2009) (25)
- Evidence for SNP‐SNP interaction identified through targeted sequencing of cleft case‐parent trios (2017) (24)
- Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population (2013) (24)
- Revisiting the recurrence risk of nonsyndromic cleft lip with or without cleft palate (2010) (24)
- Novel Cleft Susceptibility Genes in Chromosome 6q (2010) (24)
- Exploring the genomic basis of early childhood caries: a pilot study (2017) (24)
- Toward a genetic understanding of dental fear: evidence of heritability (2017) (24)
- Multi-Dimensional Prioritization of Dental Caries Candidate Genes and Its Enriched Dense Network Modules (2013) (24)
- 3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis (2006) (23)
- Women Are More Susceptible to Caries but Individuals Born with Clefts Are Not (2011) (23)
- Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. (2017) (23)
- Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries (2015) (23)
- Hair whorls and handedness: Informative phenotypic markers in nonsyndromic cleft lip with or without cleft palate (NS CL/P) cases and their unaffected relatives (2005) (23)
- Reduced folate carrier 1 (RFC1) is associated with cleft of the lip only. (2008) (23)
- A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals (2018) (23)
- SNPs Associated With Testosterone Levels Influence Human Facial Morphology (2018) (23)
- Genetic Association of MPPED2 and ACTN2 with Dental Caries (2014) (23)
- Human Telomere Length Correlates to the Size of the Associated Chromosome Arm (2009) (22)
- Search for genetic modifiers of IRF6 and genotype–phenotype correlations in Van der Woude and popliteal pterygium syndromes (2013) (22)
- TP63 mutation and clefting modifier genes in an EEC syndrome family (2004) (22)
- Improving Children’s Oral Health (2014) (22)
- The effects of family, dentition, and dental caries on the salivary microbiome. (2016) (22)
- Perceived social support of mothers of children with clefts. (2003) (21)
- Genetic linkage analysis of autosomal dominant congenital cataracts. (1986) (21)
- X‐chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate (2007) (21)
- A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk (2014) (20)
- Neural tube defects, methylenetetrahydrofolate reductase mutation, and north/south dietary differences in China. (1998) (20)
- Chromosome 17: gene mapping studies of cleft lip with or without cleft palate in Chinese families. (2003) (20)
- Role of TRAV locus in low caries experience (2013) (20)
- Genetic mapping of high caries experience on human chromosome 13 (2013) (20)
- Expanding the cleft phenotype: the dental characteristics of unaffected parents of Australian children with non-syndromic cleft lip and palate. (2014) (19)
- A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain (2017) (19)
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- Editorial: Genetic, Environmental and Synergistic Gene-Environment Contributions to Craniofacial Defects (2022) (0)
- The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only (2020) (0)
- DNA methylation differences in monozygotic twins with Van der Woude syndrome (2023) (0)
- Do Unaffected Parents of Children with Orofacial Clefts have Decreased Facial Integration Compared to Controls? (2019) (0)
- Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference? (2023) (0)
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