Kwong-Wai Choy (Kwong Wai Choy, Kwong Wai Choy, K W Choy)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 33

Top Venues

Prenatal diagnosis

Genes

Acta obstetricia et gynecologica Scandinavica

Genetics in medicine : official journal of the American College of Medical Genetics

Chinese University of Hong Kong

Chinese University of Hong Kong (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Chinese University of Hong Kong Sep 01 1999

Hong Kong

Associate Professor :: Obstetrics & Gynaecology

Education History

Chinese University of Hong Kong

Hong Kong

PHD :: Obstetrics & Gynaecology

Publications

Angel Hoi Wan Kwan, María Del Mar Gil, Shuwen Xue, Yvonne K Y Kwok, Doris Lau, Joanna Fung, Andrea Chan, Kwong-Wai Choy, Tak Yeung Leung, Liona C Poon
Cell-free DNA test for fetal chromosomal abnormalities in multiple pregnancies. Acta obstetricia et gynecologica Scandinavica 103 (9) (2024)
Angel Hoi Wan Kwan, María Del Mar Gil, Shuwen Xue, Yvonne K Y Kwok, Doris Lau, Joanna Fung, Andrea Chan, Kwong-Wai Choy, Tak Yeung Leung, Liona C Poon
Cell-free DNA test for fetal chromosomal abnormalities in multiple pregnancies. Acta obstetricia et gynecologica Scandinavica 103 (9) (2024)
Angel Hoi Wan Kwan, María Del Mar Gil, Shuwen Xue, Yvonne K Y Kwok, Doris Lau, Joanna Fung, Andrea Chan, Kwong-Wai Choy, Tak Yeung Leung, Liona C Poon
Cell-free DNA test for fetal chromosomal abnormalities in multiple pregnancies. Acta obstetricia et gynecologica Scandinavica 103 (9) (2024)
Angel Hoi Wan Kwan, María Del Mar Gil, Shuwen Xue, Yvonne K Y Kwok, Doris Lau, Joanna Fung, Andrea Chan, Kwong-Wai Choy, Tak Yeung Leung, Liona C Poon
Cell-free DNA test for fetal chromosomal abnormalities in multiple pregnancies. Acta obstetricia et gynecologica Scandinavica (2024)
Cheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, Wenxuan Jiang, Hon-Cheong So, Catherine McBride, Urs Maurer, Mo Zheng, Kwong-Wai Choy
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twins. Human genetics (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis (2023)
Kai Yeung Tse, Ilham Utama Surya, Rima Irwinda, Kwok-Yin Leung, Yuen Ha Ting, Ye Cao, Kwong-Wai Choy
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review. Genes 14 (6) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Kai Yeung Tse, Ilham Utama Surya, Rima Irwinda, Kwok-Yin Leung, Yuen Ha Ting, Ye Cao, Kwong-Wai Choy
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review. Genes 14 (6) (2023)
Kai Yeung Tse, Ilham Utama Surya, Rima Irwinda, Kwok-Yin Leung, Yuen Ha Ting, Ye Cao, Kwong-Wai Choy
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review. Genes 14 (6) (2023)
Ying Li, Matthew Hoi Kin Chau, Ying Xin Zhang, Yilin Zhao, Shuwen Xue, Tin-Chiu Li, Ye Cao, Zirui Dong, Kwong-Wai Choy, Jacqueline Pui Wah Chung
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. Human reproduction (Oxford, England) (2023)
Kai Yeung Tse, Ilham Utama Surya, Rima Irwinda, Kwok-Yin Leung, Yuen Ha Ting, Ye Cao, Kwong-Wai Choy
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review. Genes 14 (6) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Wing Ting Tse, Ye Cao, Pensi Ping Hei Lam, Kwok Ming Law, Kwong-Wai Choy, Yuen Ha Ting
Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene. Prenatal diagnosis 44 (2) (2023)
Yu Zheng, Lo Wong, Angel Hoi Wan Kwan, Zirui Dong, Ka Yin Kwok, Kwong-Wai Choy, Hongzheng Dai, Ye Cao
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene. Prenatal diagnosis (2023)
Keying Li, Yilin Zhao, Matthew Hoi Kin Chau, Ye Cao, Tak Yeung Leung, Yvonne K Kwok, Kwong-Wai Choy, Zirui Dong
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics. Genes 14 (7) (2023)
Yang Zeng, Lin Li, Qingchun Li, Jijun Hu, Nana Zhang, Ling Wu, Zheng Yan, Ronggui Qu, Jie Dong, Ruyi Liu, Kwong-Wai Choy, Lei Wang, Qing Sang, Yichun Guan, Biaobang Chen
Genetic screening in patients with ovarian dysfunction. Clinical genetics (2022)
Po Lam So, Shuk Yi Annie Hui, Teresa Wei Ling Ma, Wendy Shu, Amelia Pui Wah Hui, Choi Wah Kong, Tsz Kin Lo, Amanda Nim Chi Kan, Elaine Yee Ling Kan, Josephine Shuk Ching Chong, Brian Hon Yin Chung, Ho-Ming Luk, Kwong-Wai Choy, Anita Sik Yau Kan, Wing Cheong Leung
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies. Genes 13 (11) (2022)
Calli O Mitchell, Greysha Rivera-Cruz, Matthew Hoi Kin Chau, Zirui Dong, Kwong-Wai Choy, Jun Shen, Sami Amr, Anne B S Giersch, Cynthia C Morton
The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing. International journal of neonatal screening 8 (2) (2022)
Ziheng Zhou, Cong Tan, Matthew Hoi Kin Chau, Xiaosen Jiang, Ziyuan Ke, Tin-Chiu Li, Ye Cao, Yvonne K Kwok, Matthew Bellgard, Tak Yeung Leung, Kwong-Wai Choy, Zirui Dong
TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms. Nucleic acids research (2022)
Ye Cao, Matthew Hoi Kin Chau, Y Zheng, Y Zhao, Angel Hoi Wan Kwan, Shuk Yi Annie Hui, Y H Lam, T Y T Tan, Ada W T Tse, Lo Wong, Tak Yeung Leung, Z Dong, Kwong-Wai Choy
Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects. Prenatal diagnosis 42 (7) (2022)
Angel Hoi Wan Kwan, Xiaofan Zhu, María Del Mar Gil, Yvonne K Y Kwok, Yi Man Isabella Wah, Shuk Yi Annie Hui, Yuen-Ha Ting, Kwok-Ming Law, Doris Lau, Shuwen Xue, Kwong-Wai Choy, Daljit Sahota, Tak-Yeung Leung, Liona Chiu Yee Poon
Genome-Wide Cell-Free DNA Test for Fetal Chromosomal Abnormalities and Variants: Unrestricted Versus Restricted Reporting. Diagnostics (Basel, Switzerland) 12 (10) (2022)
Zirui Dong, Matthew Hoi Kin Chau, Yanyan Zhang, Zhenjun Yang, Mengmeng Shi, Yi Man Wah, Yvonne K Kwok, Tak Yeung Leung, Cynthia C Morton, Kwong-Wai Choy
Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics. Genetics in medicine : official journal of the American College of Medical Genetics 23 (7) (2021)
Natalie K L Wong, R Y K Cheung, L L Lee, Osanna Y K Wan, Kwong-Wai Choy, Symphorosa Shing Chee Chan
Women with advanced pelvic organ prolapse and levator ani muscle avulsion would significantly benefit from the use of mesh repair surgery. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2020)
Shuk Yi Annie Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong-Wai Choy, Tak Yeung Leung
The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings. Acta obstetricia et gynecologica Scandinavica 100 (2) (2020)
Xiaofan Zhu, Min Chen, Huilin Wang, Yilin Guo, Matthew Hoi Kin Chau, Huanchen Yan, Ye Cao, Yvonne Ka Yin Kwok, Jingsi Chen, Annie Shuk Yi Hui, Rui Zhang, Zhuo Meng, Yuanfang Zhu, Tak Yeung Leung, Likuan Xiong, Xiangdong Kong, Kwong-Wai Choy
Clinical utility of expanded noninvasive prenatal screening and chromosomal microarray analysis in high risk pregnancies. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2020)
Zirui Dong, Matthew Hoi Kin Chau, Yanyan Zhang, Peng Dai, Xiaofan Zhu, Tak Yeung Leung, Xiangdong Kong, Yvonne K Kwok, Paweł Stankiewicz, Sau Wai Cheung, Kwong-Wai Choy
Deciphering the complexity of simple chromosomal insertions by genome sequencing. Human genetics 140 (2) (2020)
Huanchen Yan, Xiaofan Zhu, Jingsi Chen, Ye Cao, Yvonne Ka Yin Kwok, Zihan Chen, Tak Yeung Leung, Min Chen, Kwong-Wai Choy
Noninvasive prenatal sequencing for multiple Mendelian monogenic disorders among fetuses with skeletal dysplasia or increased nuchal translucency. Prenatal diagnosis 40 (11) (2020)
Matthew Hoi Kin Chau, Huilin Wang, Yunli Lai, Yanyan Zhang, Fuben Xu, Yanqing Tang, Yanfang Wang, Zihan Chen, Tak Yeung Leung, Jacqueline Pui Wah Chung, Yvonne K Kwok, Shuk Ching Chong, Kwong-Wai Choy, Yuanfang Zhu, Likuan Xiong, Weihong Wei, Zirui Dong
Low-pass genome sequencing: a validated method in clinical cytogenetics. Human genetics 139 (11) (2020)
Matthew Hoi Kin Chau, Doris Yuk Man Lam, Xiaofan Zhu, Yvonne Ka Yin Kwok, Yuen Ha Ting, Wan Pang Chan, Mengmeng Shi, Sunny Wai Hung Cheung, Tze Kin Lau, Yves Ville, Tak Yeung Leung, Kwong-Wai Choy
The utility of genome-wide cell-free DNA screening in the prenatal diagnosis of Pallister-Killian syndrome. Prenatal diagnosis 40 (8) (2020)
Huilin Wang, Zirui Dong, Rui Zhang, Matthew Hoi Kin Chau, Zhenjun Yang, Kathy Yin Ching Tsang, Hoi Kin Wong, Baoheng Gui, Zhuo Meng, Kelin Xiao, Xiaofan Zhu, Yanfang Wang, Shaoyun Chen, Tak Yeung Leung, Sau Wai Cheung, Yvonne K Kwok, Cynthia C Morton, Yuanfang Zhu, Kwong-Wai Choy
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis. Genetics in medicine : official journal of the American College of Medical Genetics 22 (3) (2019)
Jun Shen, Andrea M Oza, Ignacio Del Castillo, Hatice Duzkale, Tatsuo Matsunaga, Arti Pandya, Hyunseok P Kang, Rebecca Mar-Heyming, Saurav Guha, Krista Moyer, Christine Lo, Margaret Kenna, John J Alexander, Yan Zhang, Yoel Hirsch, Minjie Luo, Ye Cao, Kwong-Wai Choy, Yen-Fu Cheng, Karen B Avraham, Xinhua Hu, Gema Garrido, Miguel Angel Moreno-Pelayo, John Greinwald, Kejian Zhang, Yukun Zeng, Zippora Brownstein, Lina Basel-Salmon, Bella Davidov, Moshe Frydman, Tzvi Weiden, Narasimhan Nagan, Alecia Willis, Sarah E Hemphill, Andrew R Grant, Rebecca K Siegert, Marina T DiStefano, Sami S Amr, Michael J Bamshad, Ahmad N Abou Tayoun, null null
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)

Kwong-Wai Choy.css-eqlu8i{font-size:small;padding-left:4px;} (Kwong Wai Choy, Kwong Wai Choy, K W Choy)

Publication Activity (10 Years)

Top Topics

Top Venues

Kwong-Wai Choy (Kwong Wai Choy, Kwong Wai Choy, K W Choy)