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Cell-free urinary microRNA-99a and microRNA-125b are diagnostic markers for the non-invasive screening of bladder cancer

PloS one, 2014-07, Vol.9 (7), p.e100793-e100793

2014

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Non‐invasive prenatal testing for fetal chromosomal abnormalities by low‐coverage whole‐genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

Ultrasound in obstetrics & gynecology, 2014-03, Vol.43 (3), p.254-264

2014

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The effect of solution pH and peroxide in the TiO2-induced photocatalysis of chlorinated aniline

Journal of hazardous materials, 2007-03, Vol.141 (1), p.86-91

2007

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Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

Ultrasound in obstetrics & gynecology, 2011-09, Vol.38 (3), p.314-319

2011

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The impact of human copy number variation on a new era of genetic testing

BJOG : an international journal of obstetrics and gynaecology, 2010-03, Vol.117 (4), p.391-398

2010

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MicroRNA from a 12-h versus 20-h acetylcysteine infusion for paracetamol overdose

Human & experimental toxicology, 2019-06, Vol.38 (6), p.646-654

2019

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Prevalence of levator ani muscle injury in Chinese women after first delivery

Ultrasound in obstetrics & gynecology, 2012-06, Vol.39 (6), p.704-709

2012

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Debates on fetal fraction measurement and DNA‐based noninvasive prenatal screening: time for standardisation?

BJOG : an international journal of obstetrics and gynaecology, 2016-09, Vol.123 (S3), p.31-35

2016

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Chromosomal abnormalities and neurological outcomes in fetal cerebral ventriculomegaly: a retrospective cohort analysis

Hong Kong Medical Journal, 2021-12, Vol.27 (6), p.428-436

2021

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Women's preference for non‐invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study

BJOG : an international journal of obstetrics and gynaecology, 2018-03, Vol.125 (4), p.451-459

2018

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Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range

Hong Kong Medical Journal, 2024-06, Vol.30 (3), p.218

2024

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Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

Journal of medical genetics, 2009-02, Vol.46 (2), p.123-131

2009

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Intermediate- to long-term outcomes of transvaginal mesh for treatment of Asian women with pelvic organ prolapse

Hong Kong Medical Journal, 2021-12, Vol.27 (6), p.413-421

2021

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The use of oxyhalogen in photocatalytic reaction to remove o-chloroaniline in TiO2 dispersion

Chemosphere (Oxford), 2007-02, Vol.66 (11), p.2106-2113

2007

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Expanded carrier screening using next-generation sequencing of 123 Hong Kong Chinese families: a pilot study

Hong Kong Medical Journal, 2021-06, Vol.27 (3), p.177-183

2021

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Incremental yield of whole‐genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta‐analysis

Ultrasound in obstetrics & gynecology, 2024-01, Vol.63 (1), p.15-23

2024

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Diagnostic accuracy of the BACs‐on‐Beads™ assay versus karyotyping for prenatal detection of chromosomal abnormalities: a retrospective consecutive case series

BJOG : an international journal of obstetrics and gynaecology, 2014-09, Vol.121 (10), p.1245-1252

2014

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Uptake and distribution of catechins in fetal organs following in utero exposure in rats

Human reproduction (Oxford), 2007-01, Vol.22 (1), p.280-287

2007

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RUVBL1/2 Complex Regulates Pro-Inflammatory Responses in Macrophages via Regulating Histone H3K4 Trimethylation

Frontiers in immunology, 2021-06, Vol.12, p.679184-679184

2021

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Selection of Supported Cobalt Substrates in the Presence of Oxone for the Oxidation of Monuron

Journal of agricultural and food chemistry, 2007-07, Vol.55 (14), p.5708-5713

2007

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Interactome and reciprocal activation of pathways in topical mesenchymal stem cells and the recipient cerebral cortex following traumatic brain injury

Scientific reports, 2017-07, Vol.7 (1), p.5017-13, Article 5017

2017

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SNaPshot reveals high mutation and carrier frequencies of 15 common hearing loss mutants in a Chinese newborn cohort

Clinical genetics, 2015-05, Vol.87 (5), p.467-472

2015

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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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Women with advanced pelvic organ prolapse and levator ani muscle avulsion would significantly benefit from mesh repair surgery

Ultrasound in obstetrics & gynecology, 2021-04, Vol.57 (4), p.631-638

2021

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Clinical utility of expanded non‐invasive prenatal screening and chromosomal microarray analysis in high‐risk pregnancy

Ultrasound in obstetrics & gynecology, 2021-03, Vol.57 (3), p.459-465

2021

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Cell-free urinary microRNA-99a and microRNA-125b are diagnostic markers for the non-invasive screening of bladder cancer

Non‐invasive prenatal testing for fetal chromosomal abnormalities by low‐coverage whole‐genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

The effect of solution pH and peroxide in the TiO2-induced photocatalysis of chlorinated aniline

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

The impact of human copy number variation on a new era of genetic testing

MicroRNA from a 12-h versus 20-h acetylcysteine infusion for paracetamol overdose

Prevalence of levator ani muscle injury in Chinese women after first delivery

Debates on fetal fraction measurement and DNA‐based noninvasive prenatal screening: time for standardisation?

Chromosomal abnormalities and neurological outcomes in fetal cerebral ventriculomegaly: a retrospective cohort analysis

Women's preference for non‐invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study

Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

Intermediate- to long-term outcomes of transvaginal mesh for treatment of Asian women with pelvic organ prolapse

The use of oxyhalogen in photocatalytic reaction to remove o-chloroaniline in TiO2 dispersion

Expanded carrier screening using next-generation sequencing of 123 Hong Kong Chinese families: a pilot study

Incremental yield of whole‐genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta‐analysis

Diagnostic accuracy of the BACs‐on‐Beads™ assay versus karyotyping for prenatal detection of chromosomal abnormalities: a retrospective consecutive case series

Uptake and distribution of catechins in fetal organs following in utero exposure in rats

RUVBL1/2 Complex Regulates Pro-Inflammatory Responses in Macrophages via Regulating Histone H3K4 Trimethylation

Selection of Supported Cobalt Substrates in the Presence of Oxone for the Oxidation of Monuron

Interactome and reciprocal activation of pathways in topical mesenchymal stem cells and the recipient cerebral cortex following traumatic brain injury

SNaPshot reveals high mutation and carrier frequencies of 15 common hearing loss mutants in a Chinese newborn cohort

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

Women with advanced pelvic organ prolapse and levator ani muscle avulsion would significantly benefit from mesh repair surgery

Clinical utility of expanded non‐invasive prenatal screening and chromosomal microarray analysis in high‐risk pregnancy

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