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Circulating microRNAs as specific biomarkers for breast cancer detection

PloS one, 2013-01, Vol.8 (1), p.e53141-e53141

2013

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Haematology and the Asian Patient: 51 Clinical Cases

1, 2024

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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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MicroRNA-143 is downregulated in breast cancer and regulates DNA methyltransferases 3A in breast cancer cells

Tumor biology, 2014-03, Vol.35 (3), p.2591-2598

2014

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Comparison of novel rapid diagnostic of blood culture identification and antimicrobial susceptibility testing by Accelerate Pheno system and BioFire FilmArray Blood Culture Identification and BioFire FilmArray Blood Culture Identification 2 panels

BMC microbiology, 2021-12, Vol.21 (1), p.350-350, Article 350

2021

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Application of droplet digital PCR in minimal residual disease monitoring of rare fusion transcripts and mutations in haematological malignancies

Scientific reports, 2024-03, Vol.14 (1), p.6400-6400, Article 6400

2024

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Acute promyelocytic leukaemia: population-based study of epidemiology and outcome with ATRA and oral-ATO from 1991 to 2021

BMC cancer, 2023-02, Vol.23 (1), p.141-141, Article 141

2023

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Recurrent Cytogenetic Abnormalities in Non-Hodgkin's Lymphoma and Chronic Lymphocytic Leukemia

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1541, p.279

Ma, Edmond S K

2017

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Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms

Diagnostic pathology, 2016-01, Vol.11 (12), p.11-11, Article 11

2016

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Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients

BMC cancer, 2020-11, Vol.20 (1), p.1053-10, Article 1053

2020

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Germline RECQL mutations in high risk Chinese breast cancer patients

Breast cancer research and treatment, 2016-06, Vol.157 (2), p.211-215

2016

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Quantitative analysis and diagnostic significance of methylated SLC19A3 DNA in the plasma of breast and gastric cancer patients

PloS one, 2011-07, Vol.6 (7), p.e22233-e22233

2011

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Sustained spontaneous remission in KMT2A-MLLT3 mutated myeloid sarcoma

Annals of hematology, 2023-05, Vol.102 (5), p.1271-1274

2023

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Distinct karyotypic and mutational landscape in trisomy AML

British journal of haematology, 2024-03, Vol.204 (3), p.939-944

2024

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BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing

Scientific reports, 2017-05, Vol.7 (1), p.1567-7, Article 1567

2017

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INDELseek: detection of complex insertions and deletions from next-generation sequencing data

BMC genomics, 2017-01, Vol.18 (1), p.16-16, Article 16

2017

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Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries

Journal of Medical Genetics, 2016-01, Vol.53 (1), p.15-23

2016

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Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel

The Journal of molecular diagnostics : JMD, 2016-07, Vol.18 (4), p.580-594

2016

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A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient

International journal of molecular sciences, 2021-01, Vol.22 (2), p.889

2021

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Effect on Germline Mutation Rate in a High-Risk Chinese Breast Cancer Cohort after Compliance with The National Comprehensive Cancer Network (NCCN) 2023 v.1 Testing Criteria

Cancers, 2023-05, Vol.15 (9), p.2635

2023

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Geographical prevalence of SARS-CoV-2 variants, August 2020 to July 2021

Scientific reports, 2022-03, Vol.12 (1), p.4704-4704, Article 4704

2022

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Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing

Cancer genetics, 2019-11, Vol.239, p.22-25

2019

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Double Heterozygosity for Germline Mutations in Chinese Breast Cancer Patients

Cancers, 2024-07, Vol.16 (14), p.2547

2024

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Combating antimicrobial resistance in Hong Kong: where are we and where should we go?

Hong Kong Medical Journal, 2022-12, Vol.28 (6), p.424-426

Ma, E S K

2022

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Circulating microRNAs as specific biomarkers for breast cancer detection

Haematology and the Asian Patient: 51 Clinical Cases

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

MicroRNA-143 is downregulated in breast cancer and regulates DNA methyltransferases 3A in breast cancer cells

Comparison of novel rapid diagnostic of blood culture identification and antimicrobial susceptibility testing by Accelerate Pheno system and BioFire FilmArray Blood Culture Identification and BioFire FilmArray Blood Culture Identification 2 panels

Application of droplet digital PCR in minimal residual disease monitoring of rare fusion transcripts and mutations in haematological malignancies

Acute promyelocytic leukaemia: population-based study of epidemiology and outcome with ATRA and oral-ATO from 1991 to 2021

Recurrent Cytogenetic Abnormalities in Non-Hodgkin's Lymphoma and Chronic Lymphocytic Leukemia

Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms

Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients

Germline RECQL mutations in high risk Chinese breast cancer patients

Establishment of the first World Health Organization International Genetic Reference Panel for quantitation of BCR-ABL mRNA

Quantitative analysis and diagnostic significance of methylated SLC19A3 DNA in the plasma of breast and gastric cancer patients

Sustained spontaneous remission in KMT2A-MLLT3 mutated myeloid sarcoma

Distinct karyotypic and mutational landscape in trisomy AML

BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing

INDELseek: detection of complex insertions and deletions from next-generation sequencing data

Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries

Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel

A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient

Effect on Germline Mutation Rate in a High-Risk Chinese Breast Cancer Cohort after Compliance with The National Comprehensive Cancer Network (NCCN) 2023 v.1 Testing Criteria

Geographical prevalence of SARS-CoV-2 variants, August 2020 to July 2021

Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing

Double Heterozygosity for Germline Mutations in Chinese Breast Cancer Patients

Combating antimicrobial resistance in Hong Kong: where are we and where should we go?

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