Published in Am J Med Genet on March 08, 2002
Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. Am J Hum Genet (2004) 1.32
Replacement of homologous mouse DNA sequence with pathogenic 6-base human CREB1 promoter sequence creates murine model of major depressive disorder. Am J Med Genet B Neuropsychiatr Genet (2011) 0.95
Effects of the A(-115)G variant on CREB1 promoter activity in two brain cell lines: Interactions with gonadal steroids. Am J Med Genet B Neuropsychiatr Genet (2010) 0.93
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease. Mov Disord (2011) 0.87
Effects of the G(-656)A variant on CREB1 promoter activity in a neuronal cell line: interactions with gonadal steroids and stress. Mol Psychiatry (2008) 0.84
Familiality of major depressive disorder and patterns of lifetime comorbidity. The NEMESIS and GenMood studies. A comparison of three samples. Eur Arch Psychiatry Clin Neurosci (2008) 0.79
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med (2004) 7.91
Cleft lip and palate: understanding genetic and environmental influences. Nat Rev Genet (2011) 5.41
The PhenX Toolkit: get the most from your measures. Am J Epidemiol (2011) 4.19
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip. Nat Genet (2008) 4.04
Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet (2010) 3.63
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol (2010) 3.48
Comparative meta-analysis of pharmacotherapy and behavior therapy for persistent insomnia. Am J Psychiatry (2002) 3.13
Impaired FGF signaling contributes to cleft lip and palate. Proc Natl Acad Sci U S A (2007) 2.94
Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS Genet (2005) 2.52
Anthropometric precision and accuracy of digital three-dimensional photogrammetry: comparing the Genex and 3dMD imaging systems with one another and with direct anthropometry. J Craniofac Surg (2006) 2.25
The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. Dev Biol (2011) 2.16
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet (2012) 2.15
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. Am J Hum Genet (2009) 2.07
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1. Am J Hum Genet (2002) 2.04
A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling. Nat Genet (2004) 1.87
Study protocol of the Center for Oral Health Research in Appalachia (COHRA) etiology study. BMC Oral Health (2008) 1.85
A collaborative study of the emergence and clinical features of the major depressive syndrome of Alzheimer's disease. Am J Psychiatry (2003) 1.83
MicroRNA-338 regulates local cytochrome c oxidase IV mRNA levels and oxidative phosphorylation in the axons of sympathetic neurons. J Neurosci (2008) 1.78
Genetics of recurrent early-onset major depression (GenRED): final genome scan report. Am J Psychiatry (2007) 1.76
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b. Am J Med Genet A (2003) 1.74
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatr Res (2004) 1.64
Maternal serum 25-hydroxyvitamin D concentrations are associated with small-for-gestational age births in white women. J Nutr (2010) 1.64
Elderly patients with dementia-related symptoms of severe agitation and aggression: consensus statement on treatment options, clinical trials methodology, and policy. J Clin Psychiatry (2008) 1.62
Neuroimaging of NREM sleep in primary insomnia: a Tc-99-HMPAO single photon emission computed tomography study. Sleep (2002) 1.61
Genome survey for susceptibility loci for recurrent, early-onset major depression: results at 10cM resolution. Am J Med Genet (2002) 1.59
Identification and quantitative analyses of microRNAs located in the distal axons of sympathetic neurons. RNA (2010) 1.58
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Hum Mol Genet (2009) 1.55
The Pittsburgh Fistula Classification System: a standardized scheme for the description of palatal fistulas. Cleft Palate Craniofac J (2007) 1.54
The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification. Cleft Palate Craniofac J (2006) 1.54
Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth. Pediatr Res (2007) 1.53
Revisiting the recurrence risk of nonsyndromic cleft lip with or without cleft palate. Am J Med Genet A (2010) 1.48
Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate. Am J Med Genet A (2007) 1.48
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genet Epidemiol (2011) 1.47
Replication of a genome-wide association study of birth weight in preterm neonates. J Pediatr (2011) 1.45
Effects of previous major depressive illness on cognition in Alzheimer disease patients. Am J Geriatr Psychiatry (2005) 1.44
In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genet Med (2004) 1.39
Genetics of cleft lip and cleft palate. Am J Med Genet C Semin Med Genet (2013) 1.38
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. Genet Med (2009) 1.38
Axonal and presynaptic protein synthesis: new insights into the biology of the neuron. Trends Neurosci (2002) 1.35
Gene-environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop. Genet Epidemiol (2011) 1.33
Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. Am J Hum Genet (2004) 1.32
Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis. Psychiatr Genet (2002) 1.32
Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience. Genet Epidemiol (2011) 1.29
Asian oral-facial cleft birth prevalence. Cleft Palate Craniofac J (2006) 1.28
Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression. Am J Med Genet B Neuropsychiatr Genet (2003) 1.28
Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate. Am J Med Genet A (2009) 1.26
Genetics of recurrent early-onset depression (GenRED): design and preliminary clinical characteristics of a repository sample for genetic linkage studies. Am J Med Genet B Neuropsychiatr Genet (2003) 1.26
Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America. Am J Med Genet A (2007) 1.25
Axon viability and mitochondrial function are dependent on local protein synthesis in sympathetic neurons. Cell Mol Neurobiol (2007) 1.24
Enamel formation genes influence enamel microhardness before and after cariogenic challenge. PLoS One (2012) 1.24
Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts. Genet Med (2008) 1.23
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Hum Mol Genet (2013) 1.23
Digital three-dimensional photogrammetry: evaluation of anthropometric precision and accuracy using a Genex 3D camera system. Cleft Palate Craniofac J (2004) 1.22
Role of polymorphic variants as genetic modulators of infection in neonatal sepsis. Pediatr Res (2010) 1.19
Sudden Infant Death Syndrome: review of implicated genetic factors. Am J Med Genet A (2007) 1.19
Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation. Biometrics (2011) 1.18
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. Birth Defects Res A Clin Mol Teratol (2012) 1.16
Anatomical basis for apparent subepithelial cleft lip: a histological and ultrasonographic survey of the orbicularis oris muscle. Cleft Palate Craniofac J (2007) 1.16
Neuropsychological changes and treatment compliance in older adults with sleep apnea. J Psychosom Res (2003) 1.16
Psychosocial stress and anxiety in musculoskeletal pain patients with and without depression. Gen Hosp Psychiatry (2008) 1.15
Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases. Am J Med Genet A (2008) 1.13
Regulation of axonal trafficking of cytochrome c oxidase IV mRNA. Mol Cell Neurosci (2010) 1.09
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry (2012) 1.08
Minor physical anomalies in schizophrenia: a meta-analysis. Schizophr Res (2006) 1.08
Candidate gene and locus analysis of myopia. Mol Vis (2007) 1.08
Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses. BMC Oral Health (2012) 1.07
Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: a possible marker for genetic susceptibility. Am J Med Genet A (2008) 1.06
Genome-wide association scan of dental caries in the permanent dentition. BMC Oral Health (2012) 1.06
Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India. Am J Med Genet A (2004) 1.06
Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression. Am J Med Genet (2002) 1.05
Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio. Am J Med Genet A (2004) 1.05
Use of 16S ribosomal RNA gene analyses to characterize the bacterial signature associated with poor oral health in West Virginia. BMC Oral Health (2011) 1.03
Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene. Am J Med Genet A (2003) 1.02
Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate. Am J Med Genet A (2010) 1.01
Genetic contributions to the development of retinopathy of prematurity. Pediatr Res (2009) 1.01
Local translation of ATP synthase subunit 9 mRNA alters ATP levels and the production of ROS in the axon. Mol Cell Neurosci (2011) 1.01
Nerve terminals of squid photoreceptor neurons contain a heterogeneous population of mRNAs and translate a transfected reporter mRNA. Eur J Neurosci (2004) 1.00
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P. Eur J Hum Genet (2008) 0.99
Determination of genetic predisposition to patent ductus arteriosus in preterm infants. Pediatrics (2009) 0.99
Demographic and prenatal factors of patients with cleft lip and cleft palate. A pilot study. J Am Dent Assoc (2003) 0.99
A genome wide linkage scan for cleft lip and palate and dental anomalies. Am J Med Genet A (2008) 0.99
Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genet Epidemiol (2012) 0.98
Vaginal and oral microbes, host genotype and preterm birth. Med Hypotheses (2009) 0.97
Intraobserver error associated with measurements of the hand. Am J Hum Biol (2005) 0.96
Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis. Am J Med Genet A (2003) 0.95
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). Am J Med Genet A (2013) 0.95
Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression. Am J Med Genet B Neuropsychiatr Genet (2004) 0.95
Oral health disparities in Appalachia: orthodontic treatment need and demand. J Am Dent Assoc (2008) 0.95
MicroRNA-338 regulates the axonal expression of multiple nuclear-encoded mitochondrial mRNAs encoding subunits of the oxidative phosphorylation machinery. Cell Mol Life Sci (2012) 0.94
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects. Am J Med Genet A (2005) 0.94
X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. Am J Med Genet A (2007) 0.94