Published in Am J Obstet Gynecol on June 01, 2006
Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes. Am J Obstet Gynecol (2010) 1.75
Mother's genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth. Hum Hered (2009) 1.11
All Our Babies Cohort Study: recruitment of a cohort to predict women at risk of preterm birth through the examination of gene expression profiles and the environment. BMC Pregnancy Childbirth (2010) 1.08
Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants. Am J Obstet Gynecol (2008) 1.05
Vaginal and oral microbes, host genotype and preterm birth. Med Hypotheses (2009) 0.97
The genomics of preterm birth: from animal models to human studies. Genome Med (2013) 0.95
Association of combined maternal-fetal TNF-alpha gene G308A genotypes with preterm delivery: a gene-gene interaction study. J Biomed Biotechnol (2010) 0.91
Amniotic fluid eicosanoids in preterm and term births: effects of risk factors for spontaneous preterm labor. Obstet Gynecol (2011) 0.88
No observed association for mitochondrial SNPs with preterm delivery and related outcomes. Pediatr Res (2012) 0.84
Telomere Fragment Induced Amnion Cell Senescence: A Contributor to Parturition? PLoS One (2015) 0.82
Association between interleukin-6 receptor gene variations and atherosclerotic lipid profiles among young adolescents in Taiwan. Lipids Health Dis (2011) 0.81
A population-based study of race-specific risk for placental abruption. BMC Pregnancy Childbirth (2008) 0.81
Effect of interleukin-6 polymorphism on risk of preterm birth within population strata: a meta-analysis. BMC Genet (2013) 0.81
Association of polymorphisms in natural killer cell-related genes with preterm birth. Am J Epidemiol (2013) 0.80
California Very Preterm Birth Study: design and characteristics of the population- and biospecimen bank-based nested case-control study. Paediatr Perinat Epidemiol (2012) 0.80
Ancestry informative markers and selected single nucleotide polymorphisms in immunoregulatory genes on preterm labor and preterm premature rupture of membranes: a case control study. BMC Pregnancy Childbirth (2016) 0.75
A high-density admixture map for disease gene discovery in african americans. Am J Hum Genet (2004) 10.87
The genetic structure and history of Africans and African Americans. Science (2009) 10.65
A report: the definition and classification of cerebral palsy April 2006. Dev Med Child Neurol Suppl (2007) 9.30
Proposed definition and classification of cerebral palsy, April 2005. Dev Med Child Neurol (2005) 9.19
The worldwide incidence of preterm birth: a systematic review of maternal mortality and morbidity. Bull World Health Organ (2009) 8.17
A population-based study of measles, mumps, and rubella vaccination and autism. N Engl J Med (2002) 7.14
Cell-free DNA analysis for noninvasive examination of trisomy. N Engl J Med (2015) 6.12
Rates of caesarean section: analysis of global, regional and national estimates. Paediatr Perinat Epidemiol (2007) 5.87
Moving beyond essential interventions for reduction of maternal mortality (the WHO Multicountry Survey on Maternal and Newborn Health): a cross-sectional study. Lancet (2013) 5.85
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (2013) 4.71
Bioinformatics challenges for genome-wide association studies. Bioinformatics (2010) 4.45
Genetic analysis of African populations: human evolution and complex disease. Nat Rev Genet (2002) 4.23
New strategies for identifying gene-gene interactions in hypertension. Ann Med (2002) 4.19
A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction. Genet Epidemiol (2007) 4.15
Rapid growth of a hepatocellular carcinoma and the driving mutations revealed by cell-population genetic analysis of whole-genome data. Proc Natl Acad Sci U S A (2011) 3.80
Epistasis and its implications for personal genetics. Am J Hum Genet (2009) 3.52
Traversing the conceptual divide between biological and statistical epistasis: systems biology and a more modern synthesis. Bioessays (2005) 3.47
Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status. Am J Epidemiol (2005) 3.36
The way forward. Lancet (2007) 3.28
Prediction of adverse maternal outcomes in pre-eclampsia: development and validation of the fullPIERS model. Lancet (2010) 3.15
A global reference for fetal-weight and birthweight percentiles. Lancet (2011) 3.05
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. Am J Obstet Gynecol (2012) 2.92
Failure to replicate a genetic association may provide important clues about genetic architecture. PLoS One (2009) 2.72
Complete resequencing of 40 genomes reveals domestication events and genes in silkworm (Bombyx). Science (2009) 2.68
Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. J Autism Dev Disord (2010) 2.59
Genetic epidemiologic studies of preterm birth: guidelines for research. Am J Obstet Gynecol (2007) 2.56
Causes of stillbirths and early neonatal deaths: data from 7993 pregnancies in six developing countries. Bull World Health Organ (2006) 2.50
Data simulation software for whole-genome association and other studies in human genetics. Pac Symp Biocomput (2006) 2.49
Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet (2011) 2.48
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. Am J Hum Genet (2005) 2.44
Classifications for cesarean section: a systematic review. PLoS One (2011) 2.24
Association between intake of artificially sweetened and sugar-sweetened beverages and preterm delivery: a large prospective cohort study. Am J Clin Nutr (2012) 2.24
Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study. BMC Med (2013) 2.20
Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology. Clin Chem (2005) 2.12
Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study. BMJ (2006) 2.07
Are intravenous injections of contrast media really less nephrotoxic than intra-arterial injections? Eur Radiol (2012) 2.06
Defining normal and abnormal fetal growth: promises and challenges. Am J Obstet Gynecol (2010) 2.05
Setting research priorities to reduce almost one million deaths from birth asphyxia by 2015. PLoS Med (2011) 2.01
Learning in a virtual world: experience with using second life for medical education. J Med Internet Res (2010) 2.01
Cytokines associated with bronchopulmonary dysplasia or death in extremely low birth weight infants. Pediatrics (2009) 1.98
Elevated male European and female African contributions to the genomes of African American individuals. Hum Genet (2006) 1.97
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biol (2014) 1.95
MMR vaccination and febrile seizures: evaluation of susceptible subgroups and long-term prognosis. JAMA (2004) 1.90
Cigarette smoking cessation services in outpatient substance abuse treatment programs in the United States. J Subst Abuse Treat (2007) 1.90
G protein-coupled receptor kinase 4 gene variants in human essential hypertension. Proc Natl Acad Sci U S A (2002) 1.87
Proteomic analysis using protein chips to detect biomarkers in cervical and amniotic fluid in women with intra-amniotic inflammation. J Proteome Res (2005) 1.84
Amniotic fluid chemokines and autism spectrum disorders: an exploratory study utilizing a Danish Historic Birth Cohort. Brain Behav Immun (2011) 1.83
Shadows of complexity: what biological networks reveal about epistasis and pleiotropy. Bioessays (2009) 1.82
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nat Genet (2013) 1.82
Recurrent tissue-specific mtDNA mutations are common in humans. PLoS Genet (2013) 1.77
Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes. Am J Obstet Gynecol (2010) 1.75
Association of family history of autoimmune diseases and autism spectrum disorders. Pediatrics (2009) 1.75
Sedation with midazolam for voiding cystourethrography in children: a randomised double-blind study. Pediatr Radiol (2003) 1.71
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly. Am J Hum Genet (2008) 1.70
Time trends in reported diagnoses of childhood neuropsychiatric disorders: a Danish cohort study. Arch Pediatr Adolesc Med (2007) 1.69
Accuracy of diagnostic tests to detect asymptomatic bacteriuria during pregnancy. Obstet Gynecol (2009) 1.66
World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women. Am J Obstet Gynecol (2006) 1.65
Inequities in the use of cesarean section deliveries in the world. Am J Obstet Gynecol (2012) 1.61
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Nat Genet (2011) 1.60
Nutritional interventions during pregnancy for the prevention or treatment of maternal morbidity and preterm delivery: an overview of randomized controlled trials. J Nutr (2003) 1.58
Ecogeographic genetic epidemiology. Genet Epidemiol (2009) 1.57
Genetic studies of African populations: an overview on disease susceptibility and response to vaccines and therapeutics. Hum Genet (2008) 1.57
Outdoor air pollution, preterm birth, and low birth weight: analysis of the world health organization global survey on maternal and perinatal health. Environ Health Perspect (2014) 1.57
Validity of childhood autism in the Danish Psychiatric Central Register: findings from a cohort sample born 1990-1999. J Autism Dev Disord (2009) 1.55
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet (2013) 1.55
Improving quality of care for maternal and newborn health: prospective pilot study of the WHO safe childbirth checklist program. PLoS One (2012) 1.55
Maternal dietary patterns and preterm delivery: results from large prospective cohort study. BMJ (2014) 1.54
Making stillbirths count, making numbers talk - issues in data collection for stillbirths. BMC Pregnancy Childbirth (2009) 1.54
Intake of probiotic food and risk of preeclampsia in primiparous women: the Norwegian Mother and Child Cohort Study. Am J Epidemiol (2011) 1.51
Single-nucleotide polymorphisms for diagnosis of salt-sensitive hypertension. Clin Chem (2006) 1.51
DNA extraction procedures meaningfully influence qPCR-based mtDNA copy number determination. Mitochondrion (2009) 1.50
Retracted Folic acid supplementation, dietary folate intake during pregnancy and risk for spontaneous preterm delivery: a prospective observational cohort study. BMC Pregnancy Childbirth (2013) 1.50
Human and Helicobacter pylori coevolution shapes the risk of gastric disease. Proc Natl Acad Sci U S A (2014) 1.48
Effects of blood sample handling procedures on measurable inflammatory markers in plasma, serum and dried blood spot samples. J Immunol Methods (2008) 1.47
Origin and molecular characteristics of a novel 2013 avian influenza A(H6N1) virus causing human infection in Taiwan. Clin Infect Dis (2013) 1.45
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arterioscler Thromb Vasc Biol (2014) 1.45
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet (2005) 1.44
Maternal BMI and preterm birth: a systematic review of the literature with meta-analysis. J Matern Fetal Neonatal Med (2009) 1.43
beta(2)-adrenergic receptor promoter haplotype influences spirometric response during an acute asthma exacerbation. Clin Transl Sci (2008) 1.41
Prevalence and predictors of ocular complications associated with cataract surgery in United States veterans. Ophthalmology (2010) 1.40
[In Process Citation]. Tidsskr Nor Laegeforen (2016) 1.39
Problems with genome-wide association studies. Science (2007) 1.39
Real-time PCR-assay in the delivery suite for determination of group B streptococcal colonization in a setting with risk-based antibiotic prophylaxis. J Matern Fetal Neonatal Med (2013) 1.39
Accelerating science-driven solutions to challenges in global reproductive health: a new framework for moving forward. Obstet Gynecol (2011) 1.39
Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease. Hum Mol Genet (2005) 1.38
Pre-eclampsia in low and middle income countries. Best Pract Res Clin Obstet Gynaecol (2011) 1.38
Gene profiling of keloid fibroblasts shows altered expression in multiple fibrosis-associated pathways. J Invest Dermatol (2007) 1.38
Preterm birth in Sweden 1973-2001: rate, subgroups, and effect of changing patterns in multiple births, maternal age, and smoking. Acta Obstet Gynecol Scand (2005) 1.35
Reduction in neonatal mortality in Chile between 1990 and 2000. Pediatrics (2006) 1.33
Enabling personal genomics with an explicit test of epistasis. Pac Symp Biocomput (2010) 1.33
The effects of myostatin on adipogenic differentiation of human bone marrow-derived mesenchymal stem cells are mediated through cross-communication between Smad3 and Wnt/beta-catenin signaling pathways. J Biol Chem (2008) 1.32
Role of cytokines in preterm labour and brain injury. BJOG (2005) 1.32
Applying the chronic care model to homeless veterans: effect of a population approach to primary care on utilization and clinical outcomes. Am J Public Health (2010) 1.32
Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption. Hum Hered (2007) 1.30