Published in Obstet Gynecol on October 01, 2004
Comparison of different strategies in prenatal screening for Down's syndrome: cost effectiveness analysis of computer simulation. BMJ (2009) 1.12
Noninvasive prenatal testing: the future is now. Rev Obstet Gynecol (2013) 1.10
First trimester diagnosis and screening for fetal aneuploidy. Genet Med (2008) 1.06
Screening for fetal aneuploidy and neural tube defects. Genet Med (2009) 0.98
Prenatal screening methods for aneuploidies. N Am J Med Sci (2013) 0.82
Sequential pathways of testing after first-trimester screening for trisomy 21. Obstet Gynecol (2005) 0.75
National growth charts for United Arab Emirates children with Down syndrome from birth to 15 years of age. J Epidemiol (2014) 0.75
A Cost-Effectiveness Analysis of First Trimester Non-Invasive Prenatal Screening for Fetal Trisomies in the United States. PLoS One (2015) 0.75
A multicenter, randomized trial of treatment for mild gestational diabetes. N Engl J Med (2009) 14.40
Prevention of recurrent preterm delivery by 17 alpha-hydroxyprogesterone caproate. N Engl J Med (2003) 9.57
Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index. Lancet (2012) 6.33
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Res (2013) 5.66
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B. Nat Genet (2004) 5.19
A randomized, controlled trial of magnesium sulfate for the prevention of cerebral palsy. N Engl J Med (2008) 5.11
Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med (2012) 4.97
First-trimester screening for trisomies 21 and 18. N Engl J Med (2003) 4.47
Fetal pulse oximetry and cesarean delivery. N Engl J Med (2006) 4.45
The FMR1 premutation and reproduction. Fertil Steril (2006) 3.85
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle. Nature (2012) 3.08
Transcriptional dysregulation in NIPBL and cohesin mutant human cells. PLoS Biol (2009) 2.89
A Randomized Trial of Intrapartum Fetal ECG ST-Segment Analysis. N Engl J Med (2015) 2.86
A prospective, randomized, multicenter trial of amnioreduction vs selective fetoscopic laser photocoagulation for the treatment of severe twin-twin transfusion syndrome. Am J Obstet Gynecol (2007) 2.73
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations. Am J Hum Genet (2004) 2.67
Fetal injury associated with cesarean delivery. Obstet Gynecol (2006) 2.61
Procedural risks versus theology: chorionic villus sampling for Orthodox Jews at less than 8 weeks' gestation. Am J Obstet Gynecol (2002) 2.56
Inhaled glucocorticoids during pregnancy and offspring pediatric diseases: a national cohort study. Am J Respir Crit Care Med (2011) 2.27
Research agenda for preterm birth: recommendations from the March of Dimes. Am J Obstet Gynecol (2005) 2.21
Intact fetal cells in maternal plasma: are they really there? Lancet (2003) 2.09
Nearly a third of abnormalities found after first-trimester screening are different than expected: 10-year experience from a single center. Prenat Diagn (2013) 2.06
Germline mosaicism in Cornelia de Lange syndrome. Am J Med Genet A (2012) 2.05
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance. Am J Med Genet A (2007) 2.01
Suicide risk among perinatal women who report thoughts of self-harm on depression screens. Obstet Gynecol (2015) 2.01
Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease. Bioinformatics (2009) 1.92
Noninvasive prenatal diagnosis of a fetal microdeletion syndrome. N Engl J Med (2011) 1.85
Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. Fertil Steril (2005) 1.83
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn (2009) 1.78
Over a decade of experience with preimplantation genetic diagnosis: a multicenter report. Fertil Steril (2004) 1.77
Altered global gene expression in first trimester placentas of women destined to develop preeclampsia. Placenta (2008) 1.76
Prevention of Rh alloimmunization. J Obstet Gynaecol Can (2003) 1.68
Antenatal depressive symptoms increase the likelihood of preterm birth. Am J Obstet Gynecol (2012) 1.67
Stress during pregnancy and offspring pediatric disease: A National Cohort Study. Environ Health Perspect (2011) 1.65
Risk of uterine rupture with a trial of labor in women with multiple and single prior cesarean delivery. Obstet Gynecol (2006) 1.65
Use of the Learning Curve-Cumulative Summation test for quantitative and individualized assessment of competency of a surgical procedure in obstetrics and gynecology: fetoscopic laser ablation as a model. Am J Obstet Gynecol (2010) 1.63
Trauma in pregnancy. Crit Care Med (2005) 1.62
Genetic testing of embryos: a critical need for data. Reprod Biomed Online (2005) 1.58
Association between use of antenatal magnesium sulfate in preterm labor and adverse health outcomes in infants. Am J Obstet Gynecol (2003) 1.54
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome. Am J Med Genet A (2005) 1.53
A randomized trial of amnioreduction versus septostomy in the treatment of twin-twin transfusion syndrome. Am J Obstet Gynecol (2005) 1.48
Cell-free fetal DNA in maternal blood: kinetics, source and structure. Hum Reprod Update (2004) 1.43
Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and infertility. Fertil Steril (2007) 1.42
Fetal soft markers in obstetric ultrasound. J Obstet Gynaecol Can (2005) 1.41
Estimation of time of fetal death in the second trimester by placental histopathological examination. Pediatr Dev Pathol (2003) 1.40
Antenatal corticosteroids: we continue to learn. Am J Obstet Gynecol (2004) 1.39
Management of intermittent exotropia. J Pediatr Ophthalmol Strabismus (2002) 1.38
NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet (2007) 1.37
The use of folic acid for the prevention of neural tube defects and other congenital anomalies. J Obstet Gynaecol Can (2003) 1.34
Diagnosis and characterization of fetal sacrococcygeal teratoma with prenatal MRI. AJR Am J Roentgenol (2006) 1.34
The relationship of the factor V Leiden mutation and pregnancy outcomes for mother and fetus. Obstet Gynecol (2005) 1.33
Omega-3 fatty acid supplementation to prevent recurrent preterm birth: a randomized controlled trial. Obstet Gynecol (2010) 1.31
Sacrococcygeal teratoma: prenatal assessment, fetal intervention, and outcome. J Pediatr Surg (2004) 1.31
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Hum Mol Genet (2014) 1.25
Fetal myelomeningocele repair: short-term clinical outcomes. Am J Obstet Gynecol (2003) 1.24
Digital PCR: a powerful new tool for noninvasive prenatal diagnosis? Prenat Diagn (2008) 1.24
Interlaboratory comparison of fetal male DNA detection from common maternal plasma samples by real-time PCR. Clin Chem (2004) 1.23
Follow-up of children exposed in utero to 17 alpha-hydroxyprogesterone caproate compared with placebo. Obstet Gynecol (2007) 1.21
Projected mesothelioma incidence in men in New South Wales. Occup Environ Med (2007) 1.20
Transcription factor FIGLA is mutated in patients with premature ovarian failure. Am J Hum Genet (2008) 1.20
Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancy-associated plasma protein A, and nuchal translucency with intrauterine growth restriction and other adverse pregnancy outcomes. Am J Obstet Gynecol (2004) 1.19
Long-term outcomes in children treated by prenatal vesicoamniotic shunting for lower urinary tract obstruction. Obstet Gynecol (2005) 1.19
Randomized clinical trial of metronidazole plus erythromycin to prevent spontaneous preterm delivery in fetal fibronectin-positive women. Obstet Gynecol (2003) 1.17
Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements. Am J Med Genet A (2005) 1.14
In utero limb salvage: fetoscopic release of amniotic bands for threatened limb amputation. J Pediatr Surg (2003) 1.13
Congenital high airway obstruction syndrome: MR/US findings, effect on management, and outcome. Pediatr Radiol (2008) 1.12
Over a decade of experience with preimplantation genetic diagnosis. Fertil Steril (2004) 1.12
Pre-eclampsia and expression of heparin-binding EGF-like growth factor. Lancet (2002) 1.11
Liver position and lung-to-head ratio for prediction of extracorporeal membrane oxygenation and survival in isolated left congenital diaphragmatic hernia. Am J Obstet Gynecol (2007) 1.10
4-1BB co-stimulation enhances human CD8(+) T cell priming by augmenting the proliferation and survival of effector CD8(+) T cells. Int Immunol (2002) 1.10
Neuraxial Anesthesia in Parturients with Thrombocytopenia: A Multisite Retrospective Cohort Study. Anesth Analg (2015) 1.09
Lower extremity neuromotor function and short-term ambulatory potential following in utero myelomeningocele surgery. Fetal Diagn Ther (2009) 1.09