Search Results - "Allen Hogge, W"

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    Altered Global Gene Expression in First Trimester Placentas of Women Destined to Develop Preeclampsia by Founds, S.A, Conley, Y.P, Lyons-Weiler, J.F, Jeyabalan, A, Allen Hogge, W, Conrad, K.P

    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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    Journal Article
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    Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome by Peters, David, Chu, Tianjiao, Yatsenko, Svetlana A, Hendrix, Nancy, Hogge, W. Allen, Surti, Urvashi, Bunce, Kimberly, Dunkel, Mary, Shaw, Patricia, Rajkovic, Aleksandar

    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 by Chu, Tianjiao, Burke, Brian, Bunce, Kimberly, Surti, Urvashi, Allen Hogge, W., Peters, David G.

    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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    Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease by Chu, Tianjiao, Bunce, Kimberly, Hogge, W. Allen, Peters, David G.

    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 by Chu, Tianjiao, Shaw, Patricia A, Yeniterzi, Suveyda, Dunkel, Mary, Rajkovic, Aleksander, Hogge, W Allen, Bunce, Kimberly D, Peters, David G

    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 by Chu, Tianjiao, Handley, Daniel, Bunce, Kimberly, Surti, Urvashi, Hogge, W Allen, Peters, David G

    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? by Hogge, W. Allen, MD, Prosen, Tracy L., MD, Lanasa, Mark C., MD, PhD, Huber, Heather A., BS, Reeves, Matthew F., MD, MPH

    “…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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    Accuracy of prenatal diagnosis of isolated aqueductal stenosis by Emery, Stephen P., Hogge, W. Allen, Hill, Lyndon M.

    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 by Chu, Tianjiao, Yeniterzi, Suveyda, Rajkovic, Aleksandar, Hogge, W. Allen, Dunkel, Mary, Shaw, Patricia, Bunce, Kimberly, Peters, David G.

    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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    Comprehensive analysis of HLA-G: implications for recurrent spontaneous abortion by Berger, Dara S, Hogge, W Allen, Barmada, M Michael, Ferrell, Robert E

    “…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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    Statistical considerations for digital approaches to non-invasive fetal genotyping by Chu, Tianjiao, Bunce, Kimberly, Hogge, W. Allen, Peters, David G.

    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 by Liao, Jun, Sathanoori, Malini, Yatsenko, Svetlana A., Hu, Jie, Kochmar, Sally J., Hoffner, Lori, Hogge, W. Allen, Surti, Urvashi

    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 by Jari, Shama D, Fraer, Luanne M, Hogge, W Allen

    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 by Berger, Dara S., Merhi, Zaher, Hogge, W. Allen, Ferrell, Robert E.

    “…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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