Published in PLoS One on May 30, 2013
A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Pediatrics (2013) 1.15
Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia. Am J Respir Crit Care Med (2015) 0.89
Copy number variation in bronchopulmonary dysplasia. Am J Med Genet A (2014) 0.79
Eliciting parental support for the use of newborn blood spots for pediatric research. BMC Med Res Methodol (2016) 0.76
Genome-wide DNA methylation profiling with MeDIP-seq using archived dried blood spots. Clin Epigenetics (2016) 0.75
Superparamagnetic-bead Based Method: An Effective DNA Extraction from Dried Blood Spots (DBS) for Diagnostic PCR. J Clin Diagn Res (2014) 0.75
Hi-Plex targeted sequencing is effective using DNA derived from archival dried blood spots. Anal Biochem (2014) 0.75
Robustness of comprehensive DNA- and RNA-based assays at diagnosis of acute myeloid leukemia using blood and bone marrow stored on filter cards. Leukemia (2016) 0.75
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Whole-genome genotyping with the single-base extension assay. Nat Methods (2006) 6.66
BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques (2002) 5.98
Use of filter paper for the collection and analysis of human whole blood specimens. J Nutr (2001) 3.85
Utility of PCR for DNA analysis from dried blood spots on filter paper blotters. PCR Methods Appl (1991) 1.68
Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources. Cancer Epidemiol Biomarkers Prev (2006) 1.45
Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards. Pediatr Res (2001) 1.40
Phenylketonuria screening registry as a resource for population genetic studies. J Med Genet (2005) 1.38
The role of regional collaboratives: the California Perinatal Quality Care Collaborative model. Clin Perinatol (2010) 1.38
Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems. Genet Test (2007) 1.30
Assessing quality and functionality of DNA from fresh and archival dried blood spots and recommendations for quality control guidelines. Clin Chem (2007) 1.26
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source. BMC Genet (2011) 1.25
The CBC: reference ranges for neonates. Semin Perinatol (2009) 1.22
Genome-wide scans using archived neonatal dried blood spot samples. BMC Genomics (2009) 1.20
High-throughput genotyping on archived dried blood spot samples. Genet Test Mol Biomarkers (2009) 1.18
Stability of genomic DNA in dried blood spots stored on filter paper. Southeast Asian J Trop Med Public Health (2005) 1.16
Analysis of multiple single nucleotide polymorphisms (SNP) on DNA traces from plasma and dried blood samples. J Immunol Methods (2007) 1.06
Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA. Electrophoresis (2009) 1.04
Whole genome amplification and genetic analysis after extraction of proteins from dried blood spots. Clin Chem (2007) 0.93
Rapid, efficient method for multiplex amplification from filter paper. Hum Mutat (1998) 0.91
A simple method for extraction and purification of genomic DNA from dried blood spots on filter paper. Southeast Asian J Trop Med Public Health (2003) 0.82
Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy. N Engl J Med (2005) 13.96
Gene expression during the life cycle of Drosophila melanogaster. Science (2002) 11.36
Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics (2002) 9.87
Trends in neonatal morbidity and mortality for very low birthweight infants. Am J Obstet Gynecol (2007) 6.68
The branching programme of mouse lung development. Nature (2008) 4.73
Changes in pathogens causing early-onset sepsis in very-low-birth-weight infants. N Engl J Med (2002) 4.62
Tube morphogenesis: making and shaping biological tubes. Cell (2003) 4.54
Coronary arteries form by developmental reprogramming of venous cells. Nature (2010) 3.95
Ambient air pollution and risk of birth defects in Southern California. Am J Epidemiol (2002) 3.43
Genome-wide identification of mRNAs associated with the translational regulator PUMILIO in Drosophila melanogaster. Proc Natl Acad Sci U S A (2006) 3.27
Developmental control of blood cell migration by the Drosophila VEGF pathway. Cell (2002) 3.12
Targeting Robo4-dependent Slit signaling to survive the cytokine storm in sepsis and influenza. Sci Transl Med (2010) 3.02
Inhaled nitric oxide for premature infants with severe respiratory failure. N Engl J Med (2005) 2.81
A Randomized Trial of Phototherapy with Filtered Sunlight in African Neonates. N Engl J Med (2015) 2.73
Branching morphogenesis of the Drosophila tracheal system. Annu Rev Cell Dev Biol (2003) 2.50
Prepregnancy obesity as a risk factor for structural birth defects. Arch Pediatr Adolesc Med (2007) 2.43
Cellular and genetic analysis of wound healing in Drosophila larvae. PLoS Biol (2004) 2.39
Neural tube defects and folate: case far from closed. Nat Rev Neurosci (2006) 2.30
Panhematin provides a therapeutic benefit in experimental pancreatitis. Gut (2010) 2.23
Social interactions among epithelial cells during tracheal branching morphogenesis. Nature (2006) 2.15
serpentine and vermiform encode matrix proteins with chitin binding and deacetylation domains that limit tracheal tube length in Drosophila. Curr Biol (2006) 1.97
Prevalence of spina bifida and anencephaly during the transition to mandatory folic acid fortification in the United States. Teratology (2002) 1.94
Control selection and participation in an ongoing, population-based, case-control study of birth defects: the National Birth Defects Prevention Study. Am J Epidemiol (2009) 1.93
Dual origin of tissue-specific progenitor cells in Drosophila tracheal remodeling. Science (2008) 1.88
The continuing challenge of understanding, preventing, and treating neural tube defects. Science (2013) 1.86
Interobserver reliability and accuracy of cranial ultrasound scanning interpretation in premature infants. J Pediatr (2007) 1.79
Selection of potential therapeutics based on in vivo spatiotemporal transcription patterns of heme oxygenase-1. J Mol Med (Berl) (2002) 1.70
Heme oxygenase-1 deficiency leads to disrupted response to acute stress in stem cells and progenitors. Blood (2008) 1.70
Neural tube defects and maternal folate intake among pregnancies conceived after folic acid fortification in the United States. Am J Epidemiol (2008) 1.69
Laparotomy versus peritoneal drainage for necrotizing enterocolitis or isolated intestinal perforation in extremely low birth weight infants: outcomes through 18 months adjusted age. Pediatrics (2006) 1.69
Whole-body hypothermia for neonatal encephalopathy: animal observations as a basis for a randomized, controlled pilot study in term infants. Pediatrics (2002) 1.66
Circulating blood cells function as a surveillance system for damaged tissue in Drosophila larvae. Proc Natl Acad Sci U S A (2008) 1.65
Maternal smoking and the risk of orofacial clefts: Susceptibility with NAT1 and NAT2 polymorphisms. Epidemiology (2004) 1.63
Reduction in red blood cell transfusions among preterm infants: results of a randomized trial with an in-line blood gas and chemistry monitor. Pediatrics (2005) 1.61
Phototherapy: current methods and future directions. Semin Perinatol (2004) 1.58
To tap or not to tap: high likelihood of meningitis without sepsis among very low birth weight infants. Pediatrics (2004) 1.56
Requirement for chitin biosynthesis in epithelial tube morphogenesis. Proc Natl Acad Sci U S A (2005) 1.56
Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. Am J Med Genet A (2009) 1.55
Schizencephaly: heterogeneous etiologies in a population of 4 million California births. Am J Med Genet A (2005) 1.55
Aggressive vs. conservative phototherapy for infants with extremely low birth weight. N Engl J Med (2008) 1.49
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism. Hepatology (2002) 1.49
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects. Am J Med Genet A (2013) 1.48
Prevalence of spina bifida among children and adolescents in 10 regions in the United States. Pediatrics (2010) 1.43
Diacylglycerol kinase K variants impact hypospadias in a California study population. J Urol (2012) 1.43
Progenitor outgrowth from the niche in Drosophila trachea is guided by FGF from decaying branches. Science (2014) 1.43
Epidemiologic characteristics of congenital diaphragmatic hernia among 2.5 million California births, 1989-1997. Birth Defects Res A Clin Mol Teratol (2006) 1.43
Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. Am J Med Genet A (2010) 1.40
Hypospadias in California: trends and descriptive epidemiology. Epidemiology (2003) 1.39
Functions of the nonsense-mediated mRNA decay pathway in Drosophila development. PLoS Genet (2006) 1.36
Predischarge screening for severe neonatal hyperbilirubinemia identifies infants who need phototherapy. J Pediatr (2012) 1.34
Maternal corticosteroid use and orofacial clefts. Am J Obstet Gynecol (2007) 1.34
Continuous, noninvasive, and localized microvascular tissue oximetry using visible light spectroscopy. Anesthesiology (2004) 1.32
Neural tube defects and maternal residential proximity to agricultural pesticide applications. Am J Epidemiol (2006) 1.31
Anencephaly and spina bifida among Hispanics: maternal, sociodemographic, and acculturation factors in the National Birth Defects Prevention Study. Birth Defects Res A Clin Mol Teratol (2009) 1.31
Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2. Eur J Hum Genet (2006) 1.29
Parenteral glutamine supplementation does not reduce the risk of mortality or late-onset sepsis in extremely low birth weight infants. Pediatrics (2004) 1.27
Monitoring age-related susceptibility of young mice to oral Salmonella enterica serovar Typhimurium infection using an in vivo murine model. Pediatr Res (2005) 1.26
Agenesis of the corpus callosum in California 1983-2003: a population-based study. Am J Med Genet A (2008) 1.25
Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis. Birth Defects Res A Clin Mol Teratol (2006) 1.25
Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab (2003) 1.25
Comprehensive EMX2 genotyping of a large schizencephaly case series. Am J Med Genet A (2007) 1.22
Integration of DNA sample collection into a multi-site birth defects case-control study. Teratology (2002) 1.22
Determination of carbon monoxide (CO) in rodent tissue: effect of heme administration and environmental CO exposure. Anal Biochem (2005) 1.22
The association of ambient air pollution and traffic exposures with selected congenital anomalies in the San Joaquin Valley of California. Am J Epidemiol (2013) 1.21
Increasing prevalence of gastroschisis: population-based study in California. J Pediatr (2008) 1.21
Predictive value of an early amplitude integrated electroencephalogram and neurologic examination. Pediatrics (2011) 1.21
Neonatal microstructural development of the internal capsule on diffusion tensor imaging correlates with severity of gait and motor deficits. Dev Med Child Neurol (2007) 1.21
Heme oxygenase-2 protects against lipid peroxidation-mediated cell loss and impaired motor recovery after traumatic brain injury. J Neurosci (2003) 1.20
Bayesian methods for correcting misclassification: an example from birth defects epidemiology. Epidemiology (2009) 1.19
Myb promotes centriole amplification and later steps of the multiciliogenesis program. Development (2013) 1.17
Environmental and genetic contributors to hypospadias: a review of the epidemiologic evidence. Birth Defects Res A Clin Mol Teratol (2012) 1.17
Folic acid in early pregnancy: a public health success story. FASEB J (2010) 1.16
Risk factors for early death among extremely low-birth-weight infants. Am J Obstet Gynecol (2002) 1.16
Characterization of coelenterazine analogs for measurements of Renilla luciferase activity in live cells and living animals. Mol Imaging (2004) 1.16
Cytokines and neurodevelopmental outcomes in extremely low birth weight infants. J Pediatr (2011) 1.16
Maternal occupational exposure to polycyclic aromatic hydrocarbons: effects on gastroschisis among offspring in the National Birth Defects Prevention Study. Environ Health Perspect (2012) 1.16
Radial construction of an arterial wall. Dev Cell (2012) 1.16
Drosophila talin and integrin genes are required for maintenance of tracheal terminal branches and luminal organization. Development (2006) 1.15
A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Pediatrics (2013) 1.15
Maternal periconceptional smoking and alcohol consumption and risk for select congenital anomalies. Birth Defects Res A Clin Mol Teratol (2008) 1.15
Neural tube defects: an analysis of neighbourhood- and individual-level socio-economic characteristics. Paediatr Perinat Epidemiol (2009) 1.14
Readmission for neonatal jaundice in California, 1991-2000: trends and implications. Pediatrics (2008) 1.14
Maternal reproductive and demographic characteristics as risk factors for hypospadias. Paediatr Perinat Epidemiol (2007) 1.13
Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-N-transferase 1 (NAT1), and risk for orofacial clefts. Birth Defects Res A Clin Mol Teratol (2004) 1.13
Promoting antenatal steroid use for fetal maturation: results from the California Perinatal Quality Care Collaborative. J Pediatr (2006) 1.07
Imbalance between production and conjugation of bilirubin: a fundamental concept in the mechanism of neonatal jaundice. Pediatrics (2002) 1.06
Cesarean delivery rates and neonatal morbidity in a low-risk population. Obstet Gynecol (2004) 1.06
Neonatal brain structure on MRI and diffusion tensor imaging, sex, and neurodevelopment in very-low-birthweight preterm children. Dev Med Child Neurol (2009) 1.06
Maternal stressful life events and risks of birth defects. Epidemiology (2007) 1.06
A systematic screen for tube morphogenesis and branching genes in the Drosophila tracheal system. PLoS Genet (2011) 1.06
Socio-economic status and risk of conotruncal heart defects and orofacial clefts. Paediatr Perinat Epidemiol (2003) 1.05
Heptavalent pneumococcal conjugate vaccine immunogenicity in very-low-birth-weight, premature infants. Pediatr Infect Dis J (2010) 1.05
Whole genome microarray analysis, from neonatal blood cards. BMC Genet (2009) 1.05
Population-based analysis of left- and right-sided diaphragmatic hernias demonstrates different frequencies of selected additional anomalies. Am J Med Genet A (2007) 1.05
Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts? Am J Med Genet A (2005) 1.04
Maternal prepregnancy body mass index and risk of spontaneous preterm birth. Paediatr Perinat Epidemiol (2014) 1.04