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A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection

PloS one, 2016-01, Vol.11 (1), p.e0146997-e0146997

2016

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Noninvasive prediction of axillary lymph node status in breast cancer using promoter profiling of circulating cell-free DNA

Journal of translational medicine, 2022-12, Vol.20 (1), p.557-557, Article 557

2022

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Plasma-Derived Extracellular Vesicles Circular RNAs Serve as Biomarkers for Breast Cancer Diagnosis

Frontiers in oncology, 2021-11, Vol.11, p.752651-752651

2021

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Translated Long Non-Coding Ribonucleic Acid ZFAS1 Promotes Cancer Cell Migration by Elevating Reactive Oxygen Species Production in Hepatocellular Carcinoma

Frontiers in genetics, 2019-11, Vol.10, p.1111-1111

2019

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Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing

Molecular medicine reports, 2020-08, Vol.22 (2), p.1269-1276

2020

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Targeted Next-Generation Sequencing of Circulating Tumor DNA Mutations among Metastatic Breast Cancer Patients

Current oncology (Toronto), 2021-06, Vol.28 (4), p.2326-2336

2021

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Association between the nucleosome footprint of plasma DNA and neoadjuvant chemotherapy response for breast cancer

NPJ breast cancer, 2021-03, Vol.7 (1), p.35-35, Article 35

2021

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Simultaneous detection of target CNVs and SNVs of thalassemia by multiplex PCR and next‑generation sequencing

Molecular medicine reports, 2019-04, Vol.19 (4), p.2837-2848

2019

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Risk-association of DNA methyltransferases polymorphisms with gastric cancer in the Southern Chinese population

International journal of molecular sciences, 2012-07, Vol.13 (7), p.8364-8378

2012

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RBPTD: a database of cancer-related RNA-binding proteins in humans

Database : the journal of biological databases and curation, 2020, Vol.2020

2020

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Development of a high-throughput and sensitive assay of fusion genes in lung cancer by array-based MALDI-TOFMS

RSC advances, 2018-01, Vol.8 (49), p.27935-27945

2018

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Low-Coverage Sequencing of Urine Sediment DNA for Detection of Copy Number Aberrations in Bladder Cancer

Cancer management and research, 2021-01, Vol.13, p.1943-1953

2021

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Genetic polymorphisms in estrogen-related genes and the risk of breast cancer among Han Chinese women

International journal of molecular sciences, 2015-02, Vol.16 (2), p.4121-4135

2015

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Noninvasive prediction of response to cancer therapy using promoter profiling of circulating cell‐free DNA

Clinical and translational medicine, 2020-09, Vol.10 (5), p.e174-n/a

2020

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A Deep-Learning Pipeline for TSS Coverage Imputation From Shallow Cell-Free DNA Sequencing

Frontiers in medicine, 2021-12, Vol.8, p.684238-684238

2021

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Oncogene mutational analysis in Chinese gastrointestinal stromal tumor patients

OncoTargets and therapy, 2018-01, Vol.11, p.2279-2286

2018

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CHRNA3 polymorphism modifies lung adenocarcinoma risk in the Chinese Han population

International journal of molecular sciences, 2014-03, Vol.15 (4), p.5446-5457

2014

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A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response

Cancer medicine (Malden, MA), 2018-08, Vol.7 (8), p.3848-3861

2018

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Noninvasive inferring expressed genes and in vivo monitoring of the physiology and pathology of pregnancy using cell-free DNA

American journal of obstetrics and gynecology, 2021-03, Vol.224 (3), p.300.e1-300.e9

2021

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Aberrant methylation and downregulation of sall3 in human hepatocellular carcinoma

World journal of gastroenterology : WJG, 2012-06, Vol.18 (21), p.2719-2726

2012

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A functional variant of NEDD4L is associated with obesity and related phenotypes in a Han population of Southern China

International journal of molecular sciences, 2013-04, Vol.14 (4), p.7433-7444

2013

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Noninvasive discrimination of benign and malignant breast lesions using genome-wide nucleosome profiles of plasma cell-free DNA

Clinica chimica acta, 2021-09, Vol.520, p.95-100

2021

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Breast cancer association studies in a Han Chinese population using 10 European-ancestry-associated breast cancer susceptibility SNPs

Asian Pacific journal of cancer prevention : APJCP, 2014-01, Vol.15 (1), p.85-91

2014

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Neurogenic locus notch homolog protein 4 and brain-derived neurotrophic factor variants combined effect on schizophrenia susceptibility

Acta neuropsychiatrica, 2013-12, Vol.25 (6), p.356-360

2013

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A Genotype Signature for Predicting Pathologic Complete Response in Locally Advanced Rectal Cancer

International journal of radiation oncology, biology, physics, 2021-06, Vol.110 (2), p.482-491

2021

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A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection

Noninvasive prediction of axillary lymph node status in breast cancer using promoter profiling of circulating cell-free DNA

Plasma-Derived Extracellular Vesicles Circular RNAs Serve as Biomarkers for Breast Cancer Diagnosis

Translated Long Non-Coding Ribonucleic Acid ZFAS1 Promotes Cancer Cell Migration by Elevating Reactive Oxygen Species Production in Hepatocellular Carcinoma

Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing

Targeted Next-Generation Sequencing of Circulating Tumor DNA Mutations among Metastatic Breast Cancer Patients

Association between the nucleosome footprint of plasma DNA and neoadjuvant chemotherapy response for breast cancer

Simultaneous detection of target CNVs and SNVs of thalassemia by multiplex PCR and next‑generation sequencing

Risk-association of DNA methyltransferases polymorphisms with gastric cancer in the Southern Chinese population

RBPTD: a database of cancer-related RNA-binding proteins in humans

Development of a high-throughput and sensitive assay of fusion genes in lung cancer by array-based MALDI-TOFMS

Low-Coverage Sequencing of Urine Sediment DNA for Detection of Copy Number Aberrations in Bladder Cancer

Genetic polymorphisms in estrogen-related genes and the risk of breast cancer among Han Chinese women

Noninvasive prediction of response to cancer therapy using promoter profiling of circulating cell‐free DNA

A Deep-Learning Pipeline for TSS Coverage Imputation From Shallow Cell-Free DNA Sequencing

Oncogene mutational analysis in Chinese gastrointestinal stromal tumor patients

CHRNA3 polymorphism modifies lung adenocarcinoma risk in the Chinese Han population

A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response

Noninvasive inferring expressed genes and in vivo monitoring of the physiology and pathology of pregnancy using cell-free DNA

Aberrant methylation and downregulation of sall3 in human hepatocellular carcinoma

A functional variant of NEDD4L is associated with obesity and related phenotypes in a Han population of Southern China

Noninvasive discrimination of benign and malignant breast lesions using genome-wide nucleosome profiles of plasma cell-free DNA

Breast cancer association studies in a Han Chinese population using 10 European-ancestry-associated breast cancer susceptibility SNPs

Neurogenic locus notch homolog protein 4 and brain-derived neurotrophic factor variants combined effect on schizophrenia susceptibility

A Genotype Signature for Predicting Pathologic Complete Response in Locally Advanced Rectal Cancer

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