| Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis H Wang, Z Dong, R Zhang, MHK Chau, Z Yang, KYC Tsang, HK Wong, ... Genetics in Medicine 22 (3), 500-510, 2020 | 88 | 2020 |
| Prenatal diagnosis of fetuses with increased nuchal translucency by genome sequencing analysis KW Choy, H Wang, M Shi, J Chen, Z Yang, R Zhang, H Yan, Y Wang, ... Frontiers in Genetics 10, 761, 2019 | 64 | 2019 |
| Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis MHK Chau, Y Cao, YKY Kwok, S Chan, YM Chan, H Wang, Z Yang, ... American Journal of Obstetrics and Gynecology 221 (5), 493. e1-493. e11, 2019 | 42 | 2019 |
| Low-pass genome sequencing: a validated method in clinical cytogenetics MHK Chau, H Wang, Y Lai, Y Zhang, F Xu, Y Tang, Y Wang, Z Chen, ... Human Genetics 139, 1403-1415, 2020 | 36 | 2020 |
| Clinical utility of expanded non‐invasive prenatal screening and chromosomal microarray analysis in high‐risk pregnancy X Zhu, M Chen, H Wang, Y Guo, MHK Chau, H Yan, Y Cao, YKY Kwok, ... Ultrasound in Obstetrics & Gynecology 57 (3), 459-465, 2021 | 25 | 2021 |
| Low-pass genome sequencing–based detection of absence of heterozygosity: validation in clinical cytogenetics Z Dong, MHK Chau, Y Zhang, Z Yang, M Shi, YM Wah, YK Kwok, ... Genetics in Medicine 23 (7), 1225-1233, 2021 | 21 | 2021 |
| Deciphering the complexity of simple chromosomal insertions by genome sequencing Z Dong, MHK Chau, Y Zhang, P Dai, X Zhu, TY Leung, X Kong, YK Kwok, ... Human genetics 140, 361-380, 2021 | 17 | 2021 |
| Factors determining the uptake of influenza vaccination among children with chronic conditions JPC Chau, SHS Lo, KC Choi, MHK Chau, DWK Tong, TKY Kwong, ... The Pediatric infectious disease journal 36 (7), e197-e202, 2017 | 16 | 2017 |
| The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings AS Hui, MHK Chau, YM Chan, Y Cao, AH Kwan, X Zhu, YK Kwok, Z Chen, ... Acta Obstetricia et Gynecologica Scandinavica 100 (2), 235-243, 2021 | 15 | 2021 |
| Clinical significance of non-invasive prenatal screening for trisomy 7: cohort study and literature review X Zhu, DYM Lam, MHK Chau, S Xue, P Dai, G Zhao, Y Cao, SWH Cheung, ... Genes 12 (1), 11, 2020 | 13 | 2020 |
| Chromosome copy number variants in fetuses with syndromic malformations H Wang, MHK Chau, Y Cao, KY Kwok, KW Choy Birth Defects Research 109 (10), 725-733, 2017 | 12 | 2017 |
| Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing MHK Chau, Y Li, P Dai, M Shi, X Zhu, JPW Chung, YK Kwok, KW Choy, ... Asian journal of andrology 24 (3), 248-254, 2022 | 10 | 2022 |
| The role of chromosomal microarray and exome sequencing in prenatal diagnosis MHK Chau, KW Choy Current Opinion in Obstetrics and Gynecology 33 (2), 148-155, 2021 | 10 | 2021 |
| TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms Z Zhou, C Tan, MHK Chau, X Jiang, Z Ke, X Chen, Y Cao, YK Kwok, ... Nucleic Acids Research 51 (D1), D1168-D1178, 2023 | 9 | 2023 |
| Trio-based low-pass genome sequencing reveals characteristics and significance of rare copy number variants in prenatal diagnosis MHK Chau, J Qian, Z Chen, Y Li, Y Zheng, WT Tse, YK Kwok, TY Leung, ... Frontiers in Genetics 12, 742325, 2021 | 8 | 2021 |
| The utility of genome‐wide cell‐free DNA screening in the prenatal diagnosis of Pallister‐Killian syndrome MHK Chau, DYM Lam, X Zhu, YKY Kwok, YH Ting, WP Chan, M Shi, ... Prenatal Diagnosis 40 (8), 1005-1012, 2020 | 6 | 2020 |
| The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing CO Mitchell, G Rivera-Cruz, MHK Chau, Z Dong, KW Choy, J Shen, S Amr, ... International Journal of Neonatal Screening 8 (2), 36, 2022 | 3 | 2022 |
| Investigation of chromosomal structural abnormalities in patients with undiagnosed Neurodevelopmental Disorders Y Cao, HM Luk, Y Zhang, MHK Chau, S Xue, SSW Cheng, AM Li, ... Frontiers in genetics 13, 803088, 2022 | 2 | 2022 |
| A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester … Y Li, MHK Chau, YX Zhang, Y Zhao, S Xue, TC Li, Y Cao, Z Dong, ... Human Reproduction 38 (8), 1628-1642, 2023 | 1 | 2023 |
| Mate-pair genome sequencing reveals structural variants for idiopathic male infertility Z Dong, J Qian, TSM Law, MHK Chau, Y Cao, S Xue, S Tong, Y Zhao, ... Human Genetics 142 (3), 363-377, 2023 | 1 | 2023 |
