Search Results - "Allen Hogge, W"
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Altered Global Gene Expression in First Trimester Placentas of Women Destined to Develop Preeclampsia
Published in Placenta (Eastbourne) (01-01-2009)“…Abstract Background Preeclampsia is a pregnancy-specific disorder that remains a leading cause of maternal, fetal and neonatal morbidity and mortality, and is…”
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Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome
Published in The New England journal of medicine (10-11-2011)“…This proof-of-principle study shows that it is possible to detect a genetic microdeletion carried by a fetus through analysis of DNA in circulating maternal…”
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A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease
Published in Prenatal diagnosis (01-11-2009)“…Objectives We describe a novel microarray‐based approach for the high‐throughput discovery of epigenetic biomarkers for use in the noninvasive detection of…”
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First-Trimester Screening for Trisomies 21 and 18
Published in The New England journal of medicine (09-10-2003)“…In this multicenter study of first-trimester screening for trisomies 21 and 18, a combination of maternal age, maternal levels of free β human chorionic…”
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Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease
Published in Bioinformatics (15-05-2009)“…There is currently great interest in the development of methods for the minimally invasive diagnosis of fetal genetic disease using cell-free DNA from maternal…”
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Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing
Published in PloS one (17-03-2017)“…Minimally Invasive Karyotyping (MINK) was communicated in 2009 as a novel method for the non-invasive detection of fetal copy number anomalies in maternal…”
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Structural and regulatory characterization of the placental epigenome at its maternal interface
Published in PloS one (23-02-2011)“…Epigenetics can be loosely defined as the study of cellular "traits" that influence biological phenotype in a fashion that is not dependent on the underlying…”
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Recurrent spontaneous abortion and skewed X-inactivation: is there an association?
Published in American journal of obstetrics and gynecology (01-04-2007)“…Objective The purpose of this study was to determine whether there is an association between skewed X-inactivation and recurrent spontaneous abortion in a…”
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Sequential pathways of testing after first-trimester screening for trisomy 21
Published in Obstetrics and gynecology (New York. 1953) (01-10-2004)“…To evaluate the performance and use of second-trimester multiple-marker maternal serum screening for trisomy 21 by women who had previously undergone…”
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Accuracy of prenatal diagnosis of isolated aqueductal stenosis
Published in Prenatal diagnosis (01-04-2015)“…Objective The objective of this article is to determine the success rate of prenatally diagnosed isolated aqueductal stenosis (AS) as a first step in an…”
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High resolution non-invasive detection of a fetal microdeletion using the GCREM algorithm
Published in Prenatal diagnosis (01-05-2014)“…ABSTRACT Background/Objective The non‐invasive prenatal detection of fetal microdeletions becomes increasingly challenging as the size of the mutation…”
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Association of extreme first-trimester free human chorionic gonadotropin-β, pregnancy-associated plasma protein A, and nuchal translucency with intrauterine growth restriction and other adverse pregnancy outcomes
Published in American journal of obstetrics and gynecology (01-10-2004)“…The purpose of this study was to determine the association between first-trimester trisomy 21 screening markers (free human chorionic gonadotropin-β [hCG],…”
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Journal Article Conference Proceeding -
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Comprehensive analysis of HLA-G: implications for recurrent spontaneous abortion
Published in Reproductive sciences (Thousand Oaks, Calif.) (01-04-2010)“…Miscarriage is one of the most common pregnancy complications. Recurrent spontaneous abortion is defined as 2 or more pregnancy losses and may be associated…”
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A novel approach toward the challenge of accurately quantifying fetal DNA in maternal plasma
Published in Prenatal diagnosis (01-12-2010)Get full text
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Statistical considerations for digital approaches to non-invasive fetal genotyping
Published in Bioinformatics (15-11-2010)“…Motivation: A growing body of literature has demonstrated the potential for non-invasive diagnosis of a variety of human genetic diseases using cell-free DNA…”
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Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype
Published in Prenatal diagnosis (01-12-2012)“…ABSTRACT Objective To summarize the pregnancy outcomes of cases with mosaicism for chromosome 10q11.2 deletion detected by chorionic villus sampling (CVS) and…”
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Association of undetectable unconjugated estriol on multiple marker screening with steroid sulfatase deficiency
Published in Fetal diagnosis and therapy (01-01-2004)“…To determine whether all patients with undetectable unconjugated estriol (uE3) on multiple marker screening (MMS) are carriers for steroid sulfatase (STS)…”
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Mannose binding lectin genotypes are not associated with increased risk of unexplained recurrent pregnancy loss
Published in Journal of assisted reproduction and genetics (01-06-2013)“…Purpose Immune response to infections has been associated with recurrent pregnancy loss (RPL). Low plasma mannose binding lectin (MBL) levels, an innate…”
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Elevated first-trimester nuchal translucency increases the risk of congenital heart defects
Published in American journal of obstetrics and gynecology (01-05-2005)“…We sought to evaluate the association between first trimester nuchal translucency measurement and the risk for major congenital heart defect in chromosomally…”
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