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Kwong Wai Choy

Professor

The Chinese University of Hong Kong (CUHK)

Hong Kong

Research Interests

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Professors in Cell Biology

Articles (20)

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2026

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2025

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2023

Collaborators (5)

Silvia Paracchini

Professor

University of St. Andrews

UNITED KINGDOM

View details

Paula Jorge

Auxiliary Professor

University of Porto

PORTUGAL

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Mar Gil

Professor

Baylor College of Medicine

UNITED STATES

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Zirui Dong

Assistant Lab Director (Bioinformatics)

The Chinese University of Hong Kong (CUHK)

HONG KONG

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Matthew Hoi Kin Chau

Research Assistant Professor

The Chinese University of Hong Kong (CUHK)

CHINA

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Kwong Wai Choy

Research Interests

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Articles (20)

Global recommendations for the use of diagnostic genomic sequencing in the prenatal setting on behalf of the ESHG and ISPD

Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype–Phenotype Correlations, and Outcomes

Advances in Prenatal Cell‐Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical Implementation

A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children

Genetic Etiology in Pelvic Organ Prolapse: Role of Connective Tissue Homeostasis, Hormone Metabolism, and Oxidative Stress

Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi‐Center Cohort Study

Cell‐free DNA test for fetal chromosomal abnormalities in multiple pregnancies

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 genomic variants by genome sequencing in foetuses with central nervous system abnormalities

Functional study of a rare L1CAM gene c.1759G>C variant prove its pathogenicity

Genome sequencing in the prenatal diagnosis of structural malformations in the fetus

Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results

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

Prenatal Diagnosis and Pregnancy Outcomes of Fetuses With Orofacial Cleft: A Retrospective Cohort Study in Two Centres in Hong Kong

Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene

Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene

Thalassemia screening by third-generation sequencing: Pilot study in a Thai population

Treatment Outcomes of Cesarean Scar Pregnancy Under a Novel Classification System: A Retrospective Cohort Study

A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages

Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations

Collaborators (5)

Silvia Paracchini

Paula Jorge

Mar Gil

Zirui Dong

Matthew Hoi Kin Chau

Make your next move.

Kwong Wai Choy

Research Interests

Make your next move.

Explore related searches

Articles (20)

Global recommendations for the use of diagnostic genomic sequencing in the prenatal setting on behalf of the ESHG and ISPD

Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype–Phenotype Correlations, and Outcomes

Advances in Prenatal Cell‐Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical Implementation

A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children

Genetic Etiology in Pelvic Organ Prolapse: Role of Connective Tissue Homeostasis, Hormone Metabolism, and Oxidative Stress

Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi‐Center Cohort Study

Cell‐free DNA test for fetal chromosomal abnormalities in multiple pregnancies

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 genomic variants by genome sequencing in foetuses with central nervous system abnormalities

Functional study of a rare L1CAM gene c.1759G&gt;C variant prove its pathogenicity

Genome sequencing in the prenatal diagnosis of structural malformations in the fetus

Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results

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

Prenatal Diagnosis and Pregnancy Outcomes of Fetuses With Orofacial Cleft: A Retrospective Cohort Study in Two Centres in Hong Kong

Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene

Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene

Thalassemia screening by third-generation sequencing: Pilot study in a Thai population

Treatment Outcomes of Cesarean Scar Pregnancy Under a Novel Classification System: A Retrospective Cohort Study

A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages

Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations

Collaborators (5)

Silvia Paracchini

Paula Jorge

Mar Gil

Zirui Dong

Matthew Hoi Kin Chau

Make your next move.

Functional study of a rare L1CAM gene c.1759G>C variant prove its pathogenicity