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Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (22), p.E5106-E5114

2018

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Identification and characterization of extrachromosomal circular DNA in maternal plasma

Proceedings of the National Academy of Sciences - PNAS, 2020-01, Vol.117 (3), p.1658-1665

2020

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Detection and Characterization of Placental MicroRNAs in Maternal Plasma

Clinical chemistry (Baltimore, Md.), 2008-03, Vol.54 (3), p.482-490

2008

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Microfluidics Digital PCR Reveals a Higher than Expected Fraction of Fetal DNA in Maternal Plasma

Clinical chemistry (Baltimore, Md.), 2008-10, Vol.54 (10), p.1664-1672

2008

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High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing

Clinical chemistry (Baltimore, Md.), 2013-08, Vol.59 (8), p.1228-1237

2013

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Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing

Proceedings of the National Academy of Sciences - PNAS, 2014-12, Vol.111 (49), p.E5302-E5311

2014

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Epigenetics, fragmentomics, and topology of cell-free DNA in liquid biopsies

Science (American Association for the Advancement of Science), 2021-04, Vol.372 (6538), p.144

2021

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Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA

Clinical chemistry (Baltimore, Md.), 2013-11, Vol.59 (11), p.1583-1594

2013

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Methy-Pipe: an integrated bioinformatics pipeline for whole genome bisulfite sequencing data analysis

PloS one, 2014-06, Vol.9 (6), p.e100360-e100360

2014

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Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients

Proceedings of the National Academy of Sciences - PNAS, 2015-03, Vol.112 (11), p.E1317-E1325

2015

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Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA

Proceedings of the National Academy of Sciences - PNAS, 2019-01, Vol.116 (2), p.641-649

2019

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Noninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNA

PloS one, 2012-05, Vol.7 (5), p.e38154-e38154

2012

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Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (51), p.20458-20463

2008

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Genome-wide detection of cytosine methylation by single molecule real-time sequencing

Proceedings of the National Academy of Sciences - PNAS, 2021-02, Vol.118 (5)

2021

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Noninvasive Prenatal Diagnosis of Fetal Chromosomal Aneuploidies by Maternal Plasma Nucleic Acid Analysis

Clinical chemistry (Baltimore, Md.), 2008-03, Vol.54 (3), p.461-466

2008

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Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia Using Cell-Free Fetal DNA in Maternal Plasma

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1022-E1030

2014

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Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus

Science translational medicine, 2010-12, Vol.2 (61), p.61ra91

2010

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Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing

Proceedings of the National Academy of Sciences - PNAS, 2014-06, Vol.111 (23), p.8583-8588

2014

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Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (47), p.18761-18768

2013

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Screening of Fetal Chromosomal Aneuploidy by Noninvasive Prenatal Testing: From Innovation to Setting Public Health Agendas to Potential Impact on Other Fields

Clinical chemistry (Baltimore, Md.), 2020-01, Vol.66 (1), p.25-28

Lo, Y.M. Dennis

2020

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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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Single-Molecule Sequencing Enables Long Cell-Free DNA Detection and Direct Methylation Analysis for Cancer Patients

Clinical chemistry (Baltimore, Md.), 2022-09, Vol.68 (9), p.1151-1163

2022

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Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma

Annual review of medicine, 2016-01, Vol.67 (1), p.419-432

2016

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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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Comparison of Single Molecule, Real-Time Sequencing and Nanopore Sequencing for Analysis of the Size, End-Motif, and Tissue-of-Origin of Long Cell-Free DNA in Plasma

Clinical chemistry (Baltimore, Md.), 2023-02, Vol.69 (2), p.168-179

2023

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Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing

Identification and characterization of extrachromosomal circular DNA in maternal plasma

Detection and Characterization of Placental MicroRNAs in Maternal Plasma

Microfluidics Digital PCR Reveals a Higher than Expected Fraction of Fetal DNA in Maternal Plasma

High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing

Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing

Epigenetics, fragmentomics, and topology of cell-free DNA in liquid biopsies

Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA

Methy-Pipe: an integrated bioinformatics pipeline for whole genome bisulfite sequencing data analysis

Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients

Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA

Noninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNA

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

Genome-wide detection of cytosine methylation by single molecule real-time sequencing

Noninvasive Prenatal Diagnosis of Fetal Chromosomal Aneuploidies by Maternal Plasma Nucleic Acid Analysis

Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia Using Cell-Free Fetal DNA in Maternal Plasma

Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus

Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing

Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing

Screening of Fetal Chromosomal Aneuploidy by Noninvasive Prenatal Testing: From Innovation to Setting Public Health Agendas to Potential Impact on Other Fields

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

Single-Molecule Sequencing Enables Long Cell-Free DNA Detection and Direct Methylation Analysis for Cancer Patients

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma

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

Comparison of Single Molecule, Real-Time Sequencing and Nanopore Sequencing for Analysis of the Size, End-Motif, and Tissue-of-Origin of Long Cell-Free DNA in Plasma

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