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Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature

American journal of medical genetics. Part A, 2021-02, Vol.185 (2), p.384-389

2021

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A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies

Angewandte Chemie International Edition, 2020-06, Vol.59 (26), p.10327-10331

International ed. in English, 2020

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Polyomavirus enhancer activator 3 protein promotes breast cancer metastatic progression through Snail-induced epithelial-mesenchymal transition

The Journal of pathology, 2011-05, Vol.224 (1), p.78-89

2011

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Expanded Carrier Screening in Chinese Population - A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women

Frontiers in genetics, 2020-11, Vol.11, p.594091-594091

2020

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Hypermethylation of RAS effector related genes and DNA methyltransferase 1 expression in endometrial carcinogenesis

International journal of cancer, 2008-07, Vol.123 (2), p.296-302

2008

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Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy

Epilepsia open, 2019-03, Vol.4 (1), p.63-72

2019

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Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results

The journal of maternal-fetal & neonatal medicine, 2019-01, Vol.32 (2), p.348-350

2019

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The Role of Pea3 Group Transcription Factors in Esophageal Squamous Cell Carcinoma

The American journal of pathology, 2011-08, Vol.179 (2), p.992-1003

2011

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Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection

PloS one, 2011-12, Vol.6 (12), p.e28798-e28798

2011

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Performance of Streck cfDNA Blood Collection Tubes for Liquid Biopsy Testing

PloS one, 2016-11, Vol.11 (11), p.e0166354-e0166354

2016

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Pregnancy-associated plasma protein A (PAPP-A) to predict adverse fetal outcomes in Chinese: What is the optimal cutoff value?

Journal of obstetrics and gynaecology, 2016-10, Vol.36 (7), p.902-903

2016

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Decision outcomes of women choosing extended non-invasive prenatal testing

Journal of obstetrics and gynaecology, 2019-07, Vol.39 (5), p.733-734

2019

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Measuring Digital PCR Quality: Performance Parameters and Their Optimization

PloS one, 2016-05, Vol.11 (5), p.e0153317-e0153317

2016

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Prognostic value of circulating tumor DNA in patients with colon cancer: Systematic review

PloS one, 2017-02, Vol.12 (2), p.e0171991-e0171991

2017

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Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

PloS one, 2020-08, Vol.15 (8), p.e0238245-e0238245

2020

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The limits of personalization in precision medicine: Polygenic risk scores and racial categorization in a precision breast cancer screening trial

PloS one, 2021-10, Vol.16 (10), p.e0258571

2021

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Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening

Prenatal diagnosis, 2017-03, Vol.37 (3), p.299-302

2017

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Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing

PloS one, 2020-09, Vol.15 (9), p.e0238467

2020

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Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples

PloS one, 2018-02, Vol.13 (2), p.e0193476-e0193476

2018

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Evolution and taxonomic classification of human papillomavirus 16 (HPV16)-related variant genomes: HPV31, HPV33, HPV35, HPV52, HPV58 and HPV67

PloS one, 2011-05, Vol.6 (5), p.e20183-e20183

2011

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Non-invasive prenatal paternity testing by analysis of Y-chromosome mini-STR haplotype using next-generation sequencing

PloS one, 2022-04, Vol.17 (4), p.e0266332-e0266332

2022

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Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell® technology

PloS one, 2022-07, Vol.17 (7), p.e0271226-e0271226

2022

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Echocardiographic findings in infants with presumed congenital Zika syndrome: Retrospective case series study

PloS one, 2017-04, Vol.12 (4), p.e0175065-e0175065

2017

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Study of the extent of information desired by women undergoing non‐invasive prenatal testing following positive prenatal Down‐syndrome screening test results

International journal of gynecology and obstetrics, 2017-06, Vol.137 (3), p.338-339

2017

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Significance of the Myxovirus Resistance A (MxA) Gene — 123C>A Single-Nucleotide Polymorphism in Suppressed Interferon β Induction of Severe Acute Respiratory Syndrome Coronavirus Infection

The Journal of infectious diseases, 2010-06, Vol.201 (12), p.1899-1908

2010

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Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature

A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies

Polyomavirus enhancer activator 3 protein promotes breast cancer metastatic progression through Snail-induced epithelial-mesenchymal transition

Expanded Carrier Screening in Chinese Population - A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women

Hypermethylation of RAS effector related genes and DNA methyltransferase 1 expression in endometrial carcinogenesis

Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy

Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results

The Role of Pea3 Group Transcription Factors in Esophageal Squamous Cell Carcinoma

Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection

Performance of Streck cfDNA Blood Collection Tubes for Liquid Biopsy Testing

Pregnancy-associated plasma protein A (PAPP-A) to predict adverse fetal outcomes in Chinese: What is the optimal cutoff value?

Decision outcomes of women choosing extended non-invasive prenatal testing

Measuring Digital PCR Quality: Performance Parameters and Their Optimization

Prognostic value of circulating tumor DNA in patients with colon cancer: Systematic review

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

The limits of personalization in precision medicine: Polygenic risk scores and racial categorization in a precision breast cancer screening trial

Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening

Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing

Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples

Evolution and taxonomic classification of human papillomavirus 16 (HPV16)-related variant genomes: HPV31, HPV33, HPV35, HPV52, HPV58 and HPV67

Non-invasive prenatal paternity testing by analysis of Y-chromosome mini-STR haplotype using next-generation sequencing

Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell® technology

Echocardiographic findings in infants with presumed congenital Zika syndrome: Retrospective case series study

Study of the extent of information desired by women undergoing non‐invasive prenatal testing following positive prenatal Down‐syndrome screening test results

Significance of the Myxovirus Resistance A (MxA) Gene — 123C>A Single-Nucleotide Polymorphism in Suppressed Interferon β Induction of Severe Acute Respiratory Syndrome Coronavirus Infection

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