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Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants

American journal of obstetrics and gynecology, 2016-08, Vol.215 (2), p.227.e1-227.e16

2016

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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA

American journal of obstetrics and gynecology, 2014-10, Vol.211 (4), p.365.e1-365.e12

2014

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Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

American journal of obstetrics and gynecology, 2011-03, Vol.204 (3), p.205.e1-205.e11

2011

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DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study

Genetics in medicine, 2011-11, Vol.13 (11), p.913-920

2011

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Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma

Clinical chemistry (Baltimore, Md.), 2015-04, Vol.61 (4), p.608-616

2015

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Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts

Prenatal diagnosis, 2015-08, Vol.35 (8), p.810-815

2015

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DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

Genetics in medicine, 2012-03, Vol.14 (3), p.296-305

2012

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Oct4-Induced Pluripotency in Adult Neural Stem Cells

Cell, 2009-02, Vol.136 (3), p.411-419

2009

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Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing

Clinical biochemistry, 2013-08, Vol.46 (12), p.1099-1104

2013

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Detection of Microdeletion 22q11.2 in a Fetus by Next-Generation Sequencing of Maternal Plasma

Clinical chemistry (Baltimore, Md.), 2012-07, Vol.58 (7), p.1148-1151

2012

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Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal Testing

Clinical chemistry (Baltimore, Md.), 2018-02, Vol.64 (2), p.329-335

2018

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Quantitative High-Throughput Analysis of DNA Methylation Patterns by Base-Specific Cleavage and Mass Spectrometry

Proceedings of the National Academy of Sciences - PNAS, 2005-11, Vol.102 (44), p.15785-15790

2005

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Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma

Prenatal diagnosis, 2013-06, Vol.33 (6), p.591-597

2013

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DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

Prenatal diagnosis, 2012-08, Vol.32 (8), p.730-734

2012

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Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing

Genes & development, 2007-12, Vol.21 (23), p.3110-3122

2007

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Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice

The Journal of clinical investigation, 2009-04, Vol.119 (4), p.837-851

2009

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Quantitative DNA methylation predicts survival in adult acute myeloid leukemia

Blood, 2010-01, Vol.115 (3), p.636-642

2010

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Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination

Clinical chemistry (Baltimore, Md.), 2010-10, Vol.56 (10), p.1627-1635

2010

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Cytosine methylation profiling of cancer cell lines

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (12), p.4844-4849

2008

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High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma

PloS one, 2013-03, Vol.8 (3), p.e57381-e57381

2013

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Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing

American journal of obstetrics and gynecology, 2011-03, Vol.204 (3), p.251.e1-251.e6

2011

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Hypermethylation of Genes for Diagnosis and Risk Stratification of Prostate Cancer

Cancer investigation, 2009-01, Vol.27 (5), p.549-560

2009

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Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins

Journal of clinical medicine, 2014-06, Vol.3 (3), p.679-692

2014

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Stemness of the organ of Corti relates to the epigenetic status of Sox2 enhancers

PloS one, 2012-05, Vol.7 (5), p.e36066-e36066

2012

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Epithelial Progeny of Estrogen-Exposed Breast Progenitor Cells Display a Cancer-like Methylome

Cancer research (Chicago, Ill.), 2008-03, Vol.68 (6), p.1786-1796

2008

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Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study

Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

Oct4-Induced Pluripotency in Adult Neural Stem Cells

Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing

Detection of Microdeletion 22q11.2 in a Fetus by Next-Generation Sequencing of Maternal Plasma

Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal Testing

Quantitative High-Throughput Analysis of DNA Methylation Patterns by Base-Specific Cleavage and Mass Spectrometry

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma

DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing

Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice

Quantitative DNA methylation predicts survival in adult acute myeloid leukemia

Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination

Cytosine methylation profiling of cancer cell lines

High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma

Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing

Hypermethylation of Genes for Diagnosis and Risk Stratification of Prostate Cancer

Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins

Stemness of the organ of Corti relates to the epigenetic status of Sox2 enhancers

Epithelial Progeny of Estrogen-Exposed Breast Progenitor Cells Display a Cancer-like Methylome

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