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Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments

Proceedings of the National Academy of Sciences - PNAS, 2015-10, Vol.112 (40), p.E5503-E5512

2015

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Noninvasive twin zygosity assessment and aneuploidy detection by maternal plasma DNA sequencing

Prenatal diagnosis, 2013-07, Vol.33 (7), p.675-681

2013

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Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics

Proceedings of the National Academy of Sciences - PNAS, 2017-09, Vol.114 (37), p.E7786-E7795

2017

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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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Use of birth weight threshold for macrosomia to identify fetuses at risk of shoulder dystocia among Chinese populations

International journal of gynecology and obstetrics, 2013-03, Vol.120 (3), p.249-253

2013

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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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Systematic Selection of Reference Genes for the Normalization of Circulating RNA Transcripts in Pregnant Women Based on RNA-Seq Data

International journal of molecular sciences, 2017-08, Vol.18 (8), p.1709

2017

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Age-specific prevalence of hepatitis B virus infection in young pregnant women, Hong Kong Special Administrative Region of China

Bulletin of the World Health Organization, 2014-11, Vol.92 (11), p.782-789

2014

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Noninvasive prenatal determination of twin zygosity by maternal plasma DNA analysis

Clinical chemistry (Baltimore, Md.), 2013-02, Vol.59 (2), p.427-435

2013

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Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (50), p.E8159-E8168

2016

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Prenatal diagnosis of maternally inherited X-linked Opitz G/BBB syndrome by chromosomal microarray in a fetus with complex congenital heart disease

Clinica chimica acta, 2014-09, Vol.436, p.140-142

2014

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Cell-free DNA in maternal plasma and serum: A comparison of quantity, quality and tissue origin using genomic and epigenomic approaches

Clinical biochemistry, 2016-12, Vol.49 (18), p.1379-1386

2016

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Noninvasive prenatal testing by nanopore sequencing of maternal plasma DNA: feasibility assessment

Clinical chemistry (Baltimore, Md.), 2015-10, Vol.61 (10), p.1305-1306

2015

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Nonremoval of an abnormally invasive placenta at cesarean section with postoperative uterine artery embolization

Acta obstetricia et gynecologica Scandinavica, 2013-11, Vol.92 (11), p.1250-1255

2013

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Investigation of biological factors influencing the placental mRNA profile in maternal plasma

Prenatal diagnosis, 2014-03, Vol.34 (3), p.251-258

2014

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The detection of mosaicism by prenatal BoBs

Prenatal diagnosis, 2013-01, Vol.33 (1), p.42-49

2013

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Advanced maternal age and postpartum hemorrhage - risk factor or red herring?

The journal of maternal-fetal & neonatal medicine, 2014-02, Vol.27 (3), p.243-246

2014

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Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis

Hong Kong medical journal = Xianggang yi xue za zhi, 2017-04, Vol.23 (2), p.110-116

2017

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Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population

Hong Kong medical journal = Xianggang yi xue za zhi, 2019-02, Vol.25 (1), p.6-12

2019

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Mortality and morbidity of extremely low birth weight infants in Hong Kong, 2010-2017: a single-centre review

Hong Kong medical journal = Xianggang yi xue za zhi, 2018-10, Vol.24 (5), p.460-465

2018

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First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family

Hemoglobin, 2017-05, Vol.41 (3), p.175-179

2017

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Triplet pregnancy with fetal reduction: experience in Hong Kong

Hong Kong medical journal = Xianggang yi xue za zhi, 2017-08, Vol.23 (4), p.326-332

2017

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Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1

Hong Kong medical journal = Xianggang yi xue za zhi, 2017-04, Vol.23 (2), p.110

2017

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Efficacy and Adverse Effects of Monarc Versus Tension-free Vaginal Tape Obturator: a Retrospective One-year Follow-up Study

Hong Kong journal of gynaecology, obstetrics, and midwifery = Xianggang fu chan zhu chan ke za zhi, 2012-01, Vol.12 (1), p.50

2012

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Immunogenicity of a Third Dose of BNT162b2 to Ancestral Severe Acute Respiratory Syndrome Coronavirus 2 and the Omicron Variant in Adults Who Received 2 Doses of Inactivated Vaccine

Clinical infectious diseases, 2023-02, Vol.76 (3), p.e299-e307

2023

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Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments

Noninvasive twin zygosity assessment and aneuploidy detection by maternal plasma DNA sequencing

Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics

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

Use of birth weight threshold for macrosomia to identify fetuses at risk of shoulder dystocia among Chinese populations

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases

Systematic Selection of Reference Genes for the Normalization of Circulating RNA Transcripts in Pregnant Women Based on RNA-Seq Data

Age-specific prevalence of hepatitis B virus infection in young pregnant women, Hong Kong Special Administrative Region of China

Noninvasive prenatal determination of twin zygosity by maternal plasma DNA analysis

Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends

Prenatal diagnosis of maternally inherited X-linked Opitz G/BBB syndrome by chromosomal microarray in a fetus with complex congenital heart disease

Cell-free DNA in maternal plasma and serum: A comparison of quantity, quality and tissue origin using genomic and epigenomic approaches

Noninvasive prenatal testing by nanopore sequencing of maternal plasma DNA: feasibility assessment

Nonremoval of an abnormally invasive placenta at cesarean section with postoperative uterine artery embolization

Investigation of biological factors influencing the placental mRNA profile in maternal plasma

The detection of mosaicism by prenatal BoBs

Advanced maternal age and postpartum hemorrhage - risk factor or red herring?

Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis

Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population

Mortality and morbidity of extremely low birth weight infants in Hong Kong, 2010-2017: a single-centre review

First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family

Triplet pregnancy with fetal reduction: experience in Hong Kong

Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1

Efficacy and Adverse Effects of Monarc Versus Tension-free Vaginal Tape Obturator: a Retrospective One-year Follow-up Study

Immunogenicity of a Third Dose of BNT162b2 to Ancestral Severe Acute Respiratory Syndrome Coronavirus 2 and the Omicron Variant in Adults Who Received 2 Doses of Inactivated Vaccine

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