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Sequencing-based counting and size profiling of plasma Epstein–Barr virus DNA enhance population screening of nasopharyngeal carcinoma

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (22), p.E5115-E5124

2018

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Noninvasive Prenatal Diagnosis of Monogenic Diseases by Digital Size Selection and Relative Mutation Dosage on DNA in Maternal Plasma

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (50), p.19920-19925

2008

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Topologic Analysis of Plasma Mitochondrial DNA Reveals the Coexistence of Both Linear and Circular Molecules

Clinical chemistry (Baltimore, Md.), 2019-09, Vol.65 (9), p.1161-1170

2019

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Methylation analysis of plasma DNA informs etiologies of Epstein-Barr virus-associated diseases

Nature communications, 2019-07, Vol.10 (1), p.3256-11, Article 3256

2019

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Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers

Blood, 2017-07, Vol.130 (3), p.340-347

2017

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Plasma Epstein–Barr viral DNA load at midpoint of radiotherapy course predicts outcome in advanced-stage nasopharyngeal carcinoma

Annals of oncology, 2014-06, Vol.25 (6), p.1204-1208

2014

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Early detection of nasopharyngeal carcinoma by plasma Epstein‐Barr virus DNA analysis in a surveillance program

Cancer, 2013-05, Vol.119 (10), p.1838-1844

2013

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Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA

Blood, 2011-03, Vol.117 (13), p.3684-3691

2011

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Rapid Clearance of Fetal DNA from Maternal Plasma

American journal of human genetics, 1999, Vol.64 (1), p.218-224

1999

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Presence of fetal DNA in maternal plasma and serum

The Lancet (British edition), 1997-08, Vol.350 (9076), p.485-487

1997

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Predominant Hematopoietic Origin of Cell-free DNA in Plasma and Serum after Sex-mismatched Bone Marrow Transplantation

Clinical chemistry (Baltimore, Md.), 2002-03, Vol.48 (3), p.421-427

2002

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High resolution size analysis of fetal DNA in the urine of pregnant women by paired-end massively parallel sequencing

PloS one, 2012-10, Vol.7 (10), p.e48319-e48319

2012

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Nonhematopoietically Derived DNA Is Shorter than Hematopoietically Derived DNA in Plasma: A Transplantation Model

Clinical chemistry (Baltimore, Md.), 2012-03, Vol.58 (3), p.549-558

2012

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Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

American journal of human genetics, 1998-04, Vol.62 (4), p.768-775

1998

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Quantitative Analysis of Circulating Methylated DNA as a Biomarker for Hepatocellular Carcinoma

Clinical chemistry (Baltimore, Md.), 2008-09, Vol.54 (9), p.1528-1536

2008

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The Biology of Cell-free DNA Fragmentation and the Roles of DNASE1, DNASE1L3, and DFFB

American journal of human genetics, 2020-02, Vol.106 (2), p.202-214

2020

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Epigenetic-genetic chromosome dosage approach for fetal trisomy 21 detection using an autosomal genetic reference marker

PloS one, 2010-12, Vol.5 (12), p.e15244-e15244

2010

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Prenatal exclusion of β thalassaemia major by examination of maternal plasma

The Lancet (British edition), 2002-09, Vol.360 (9338), p.998-1000

2002

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Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

Blood, 2002-10, Vol.100 (8), p.2845-2851

2002

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Noninvasive fetal RHD genotyping by microfluidics digital PCR using maternal plasma from two alloimmunized women with the variant RHD(IVS3+1G>A) allele

Prenatal diagnosis, 2013-12, Vol.33 (12), p.1214-1216

2013

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Size Distributions of Maternal and Fetal DNA in Maternal Plasma

Clinical chemistry (Baltimore, Md.), 2004-01, Vol.50 (1), p.88-92

2004

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MS Analysis of Single-Nucleotide Differences in Circulating Nucleic Acids: Application to Noninvasive Prenatal Diagnosis

Proceedings of the National Academy of Sciences - PNAS, 2004-07, Vol.101 (29), p.10762-10767

2004

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Quantitative Abnormalities of Fetal DNA in Maternal Serum in Preeclampsia

Clinical chemistry (Baltimore, Md.), 1999-02, Vol.45 (2), p.184-188

1999

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Plasma Epstein-Barr Virus DNA and Residual Disease After Radiotherapy for Undifferentiated Nasopharyngeal Carcinoma

JNCI : Journal of the National Cancer Institute, 2002-11, Vol.94 (21), p.1614-1619

2002

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Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases

Clinical chemistry (Baltimore, Md.), 2017-02, Vol.63 (2), p.513-524

2017

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1 – 25 von 19.759

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Sequencing-based counting and size profiling of plasma Epstein–Barr virus DNA enhance population screening of nasopharyngeal carcinoma

Noninvasive Prenatal Diagnosis of Monogenic Diseases by Digital Size Selection and Relative Mutation Dosage on DNA in Maternal Plasma

Topologic Analysis of Plasma Mitochondrial DNA Reveals the Coexistence of Both Linear and Circular Molecules

Methylation analysis of plasma DNA informs etiologies of Epstein-Barr virus-associated diseases

Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers

Plasma Epstein–Barr viral DNA load at midpoint of radiotherapy course predicts outcome in advanced-stage nasopharyngeal carcinoma

Early detection of nasopharyngeal carcinoma by plasma Epstein‐Barr virus DNA analysis in a surveillance program

Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA

Rapid Clearance of Fetal DNA from Maternal Plasma

Presence of fetal DNA in maternal plasma and serum

Predominant Hematopoietic Origin of Cell-free DNA in Plasma and Serum after Sex-mismatched Bone Marrow Transplantation

High resolution size analysis of fetal DNA in the urine of pregnant women by paired-end massively parallel sequencing

Nonhematopoietically Derived DNA Is Shorter than Hematopoietically Derived DNA in Plasma: A Transplantation Model

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

Quantitative Analysis of Circulating Methylated DNA as a Biomarker for Hepatocellular Carcinoma

The Biology of Cell-free DNA Fragmentation and the Roles of DNASE1, DNASE1L3, and DFFB

Epigenetic-genetic chromosome dosage approach for fetal trisomy 21 detection using an autosomal genetic reference marker

Prenatal exclusion of β thalassaemia major by examination of maternal plasma

Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

Noninvasive fetal RHD genotyping by microfluidics digital PCR using maternal plasma from two alloimmunized women with the variant RHD(IVS3+1G>A) allele

Size Distributions of Maternal and Fetal DNA in Maternal Plasma

MS Analysis of Single-Nucleotide Differences in Circulating Nucleic Acids: Application to Noninvasive Prenatal Diagnosis

Quantitative Abnormalities of Fetal DNA in Maternal Serum in Preeclampsia

Plasma Epstein-Barr Virus DNA and Residual Disease After Radiotherapy for Undifferentiated Nasopharyngeal Carcinoma

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases

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