Published in Fetal Pediatr Pathol on May 15, 2014
Epidemiology and causes of preterm birth. Lancet (2008) 18.96
Neonatal outcomes of extremely preterm infants from the NICHD Neonatal Research Network. Pediatrics (2010) 9.15
Prophylactic administration of progesterone by vaginal suppository to reduce the incidence of spontaneous preterm birth in women at increased risk: a randomized placebo-controlled double-blind study. Am J Obstet Gynecol (2003) 6.74
The enigma of spontaneous preterm birth. N Engl J Med (2010) 6.04
Long-term medical and social consequences of preterm birth. N Engl J Med (2008) 4.68
Global report on preterm birth and stillbirth (1 of 7): definitions, description of the burden and opportunities to improve data. BMC Pregnancy Childbirth (2010) 3.89
Born too soon: the global epidemiology of 15 million preterm births. Reprod Health (2013) 3.32
Gestational age at birth and mortality in young adulthood. JAMA (2011) 3.31
Cost of hospitalization for preterm and low birth weight infants in the United States. Pediatrics (2007) 3.22
Optimizing care and outcome for late-preterm (near-term) infants: a summary of the workshop sponsored by the National Institute of Child Health and Human Development. Pediatrics (2006) 3.16
Births: preliminary data for 2012. Natl Vital Stat Rep (2013) 2.65
Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study. BMJ (2006) 2.07
The preterm prediction study: effect of gestational age and cause of preterm birth on subsequent obstetric outcome. National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network. Am J Obstet Gynecol (1999) 2.01
Placental vascular pathology findings and pathways to preterm delivery. Am J Epidemiol (2009) 1.73
The preterm birth syndrome: issues to consider in creating a classification system. Am J Obstet Gynecol (2011) 1.66
Perinatal outcomes associated with preterm birth at 33 to 36 weeks' gestation: a population-based cohort study. Pediatrics (2009) 1.37
What causes racial disparities in very preterm birth? A biosocial perspective. Epidemiol Rev (2009) 1.30
The preterm birth syndrome: a prototype phenotypic classification. Am J Obstet Gynecol (2011) 1.30
The prevalence of vaginal microorganisms in pregnant women with preterm labor and preterm birth. Ann Lab Med (2012) 1.27
Maternal age and parity-associated risks of preterm birth: differences by race/ethnicity. Paediatr Perinat Epidemiol (2007) 1.21
The Alabama Preterm Birth Project: placental histology in recurrent spontaneous and indicated preterm birth. Am J Obstet Gynecol (2006) 1.14
The long-term renal and cardiovascular consequences of prematurity. Nat Rev Nephrol (2012) 1.03
The placenta in preterm birth. J Clin Pathol (2008) 0.99
Insights in public health: saving babies: reducing infant mortality in Hawai'i. Hawaii J Med Public Health (2013) 0.96
Association of bacterial vaginosis with adverse fetomaternal outcome in women with spontaneous preterm labor: a prospective cohort study. J Matern Fetal Neonatal Med (2011) 0.90
The joint association between F5 gene polymorphisms and maternal smoking during pregnancy on preterm delivery. Hum Genet (2008) 0.90
Outcome of pregnancies among Hispanics: revisiting the epidemiologic paradox. J Reprod Med (2006) 0.89
Determinants of continuous positive airway pressure adherence in a sleep clinic cohort of South Florida Hispanic veterans. Sleep Breath (2012) 0.88
Growing up after extremely preterm birth: lifespan mental health outcomes. Semin Fetal Neonatal Med (2013) 0.87
The interaction between the maternal BMI and angiogenic gene polymorphisms associates with the risk of spontaneous preterm birth. Mol Hum Reprod (2012) 0.87
Genetic basis of preterm birth. Front Biosci (2007) 0.87
The Florida Investigation of Primary Late Preterm and Cesarean Delivery: the accuracy of the birth certificate and hospital discharge records. Matern Child Health J (2013) 0.83
Positive C4d immunostaining of placental villous syncytiotrophoblasts supports host-versus-graft rejection in villitis of unknown etiology. Pediatr Dev Pathol (2012) 0.82
The relationship of socioeconomic status to preterm contractions and preterm delivery. Matern Child Health J (2012) 0.79
Genetics and preterm birth. J Obstet Gynecol Neonatal Nurs (2013) 0.78
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature (2011) 4.56
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy. Eur J Pediatr (2007) 3.40
From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proc Natl Acad Sci U S A (2008) 3.39
The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. Am Heart J (2008) 2.61
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Am J Hum Genet (2011) 2.38
Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish. Calcif Tissue Int (2009) 1.96
Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era. Circ Cardiovasc Genet (2012) 1.78
TCF7L2 variants associate with CKD progression and renal function in population-based cohorts. J Am Soc Nephrol (2008) 1.71
Development and evaluation of quality control dried blood spot materials in newborn screening for lysosomal storage disorders. Clin Chem (2008) 1.71
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. Arch Intern Med (2010) 1.64
Newborn screening for Pompe disease by measuring acid alpha-glucosidase activity using tandem mass spectrometry. Clin Chem (2008) 1.47
Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals. Genet Med (2011) 1.34
Exercise attenuates PCB-induced changes in the mouse gut microbiome. Environ Health Perspect (2013) 1.33
Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet (2013) 1.30
Genome-wide association of body fat distribution in African ancestry populations suggests new loci. PLoS Genet (2013) 1.24
Mucopolysaccharidosis type II in females: case report and review of literature. Pediatr Neurol (2005) 1.20
Pregnancy at or beyond age 40 years is associated with an increased risk of fetal death and other adverse outcomes. Am J Obstet Gynecol (2007) 1.08
Long-term stability of amino acids and acylcarnitines in dried blood spots. Clin Chem (2007) 1.07
Influence of hematocrit and localisation of punch in dried blood spots on levels of amino acids and acylcarnitines measured by tandem mass spectrometry. Clin Chim Acta (2006) 1.06
Excessive weight gain among obese women and pregnancy outcomes. Am J Perinatol (2009) 1.06
Lysosomal storage disorder 4+1 multiplex assay for newborn screening using tandem mass spectrometry: application to a small-scale population study for five lysosomal storage disorders. Clin Chim Acta (2012) 1.05
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis (2013) 1.04
Heparin cofactor II-thrombin complex: a biomarker of MPS disease. Mol Genet Metab (2008) 1.04
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Neurobiol Aging (2012) 1.02
Role of the Nav1.7 R1150W amino acid change in susceptibility to symptomatic knee osteoarthritis and multiple regional pain. Arthritis Care Res (Hoboken) (2010) 1.02
Severe colitis associated with docetaxel use: A report of four cases. World J Gastrointest Oncol (2010) 1.01
Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations. Pediatrics (2012) 0.95
Prenatal and postnatal treatment in cobalamin C defect. J Pediatr (2005) 0.95
Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Hum Genet (2012) 0.93
Prostate sampling by 12-core biopsy: comparison of the biopsy results with tumor location in prostatectomy specimens. Urology (2011) 0.92
Outcome of pregnancies among Hispanics: revisiting the epidemiologic paradox. J Reprod Med (2006) 0.89
Transcobalamin II deficiency at birth. Mol Genet Metab (2009) 0.89
Effects of covariates: a summary of Group 5 contributions. Genet Epidemiol (2003) 0.88
Practical management of combined methylmalonicaciduria and homocystinuria. J Child Neurol (2002) 0.87
Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure. Orphanet J Rare Dis (2012) 0.86
Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometry. Mol Genet Metab (2009) 0.86
Clinically significant Gleason sum upgrade: external validation and head-to-head comparison of the existing nomograms. Cancer (2011) 0.86
Extent and distribution of linkage disequilibrium in the Old Order Amish. Genet Epidemiol (2010) 0.86
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy. J Card Fail (2013) 0.86
Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria. Eur J Pediatr (2006) 0.85
Analysis of lyso-globotriaosylsphingosine in dried blood spots. Ann Lab Med (2013) 0.85
Analysis of glucocerebrosidase activity in dry blood spots using tandem mass spectrometry. Clin Chim Acta (2010) 0.85
Analysis of acid sphingomyelinase activity in dried blood spots using tandem mass spectrometry. Ann Lab Med (2012) 0.84
The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC). Mol Genet Metab (2010) 0.84
Low levels of asymmetric dimethylarginine in children with diabetes mellitus type I compared with healthy children. J Pediatr (2010) 0.83
Intestinal candidiasis: an uncommon cause of necrotizing enterocolitis (NEC) in neonates. Fetal Pediatr Pathol (2010) 0.83
Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndrome. Am J Med Genet A (2007) 0.82
Central nervous system malformations in oral-facial-digital syndrome, type 1. Am J Med Genet A (2005) 0.81
Effects of creatine supplementation in Rett syndrome: a randomized, placebo-controlled trial. J Dev Behav Pediatr (2011) 0.80
Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria. Mol Genet Metab (2008) 0.80
Lyso-globotriaosylsphingosine (lyso-Gb3) levels in neonates and adults with the Fabry disease later-onset GLA IVS4+919G>A mutation. J Inherit Metab Dis (2012) 0.80
Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III. Mol Genet Metab (2007) 0.79
Semi-quantitative method for determination of hematocrit in dried blood spots, using data collected in HPLC hemoglobin variant testing. Clin Chim Acta (2010) 0.78
B4GALT1-congenital disorders of glycosylation presents as a non-neurologic glycosylation disorder with hepatointestinal involvement. J Pediatr (2011) 0.78
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35. Birth Defects Res A Clin Mol Teratol (2006) 0.78
T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. Am J Med Genet (2002) 0.78
Autoimmune hepatitis and primary sclerosing cholangitis in children and adolescents. Fetal Pediatr Pathol (2014) 0.78
Tumor focality is not associated with biochemical outcome after radical prostatectomy. Prostate (2011) 0.78
Diagnosing lysosomal storage disorders: mucopolysaccharidosis type i. Curr Protoc Hum Genet (2015) 0.77
Family-based genetic association tests. Cold Spring Harb Protoc (2011) 0.77
Defining a molecular portrait of physical fitness. Anal Bioanal Chem (2013) 0.76
Prognostic implications of partial sampling of radical prostatectomy specimens: comparison of 3 methods. J Urol (2012) 0.76
Patients with type 1 Gaucher disease in South Florida, USA: demographics, genotypes, disease severity and treatment outcomes. Orphanet J Rare Dis (2014) 0.76
Lack of Association between COX-2 Staining Level and Biochemical Recurrence Following Salvage Radiation Therapy for Recurrent Prostate Cancer. J Radiat Oncol (2013) 0.75
Echogenic endometrial fluid collection in postmenopausal women is a significant risk factor for disease. J Ultrasound Med (2005) 0.75
Rapid analysis of total plasma homocysteine by tandem mass spectrometry. Clin Chim Acta (2005) 0.75
Fabry disease defined. Eur J Clin Invest (2004) 0.75
Possible Genetic Origin of Limb-Body Wall Complex. Fetal Pediatr Pathol (2015) 0.75
A unique presentation and rare pathological finding for urachal sinus. J Pediatr Surg (2013) 0.75
Intracaval liver with cardiac extension. A new developmental anomaly? Fetal Pediatr Pathol (2010) 0.75
Diagnosing lysosomal storage disorders: mucopolysaccharidosis type II. Curr Protoc Hum Genet (2013) 0.75
Pediatric rhabdomyosarcoma. Ear Nose Throat J (2014) 0.75
Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiency. Clin Chem (2002) 0.75
Thrombotic cutaneous gangrene with autoamputation of the penis: a rare extracolonic manifestation of ulcerative colitis in a child. J Pediatr Surg (2009) 0.75
Quantification of sickle cells in the peripheral smear as a marker of disease severity. Fetal Pediatr Pathol (2014) 0.75