Reproductive Medicine
Research Topic
Delineating the spectrum of genomic variants in families with recurrent miscarriage
Supervisor(s)
Prof. Choy Kwong Wai Richard and Prof. Dong Zirui Elvis
ZHENG Yuting
1
Mate-pair Sequencing Enables Identification and Delineation of Balanced and Unbalanced Structural Variants in Prenatal Cytogenomic Diagnostics
Qian J, Wang H, Liang H, Zheng Y, Yu M, Tse WT, Kwan AHW, Wong L, Wong NKL, Wah IYM, Lau SL, Hui ASY, Chau MHK, Chen X, Zhang R, Poon L C, Leung TY, Liu P, Choy KW, Dong Z
Clin Chem. 2025 Jan 3;71(1):155-168
2
Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities
Wang Y, Liu M, Gao Z, Hua C, Jiang J, Zheng Y, Dong Z, Cao Y, Choy KW, Zhu X, Kong X
Ann Med. 2024 Dec;56(1):2399317
3
Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi-Center Cohort Study
Li K, Wang H, Chau MHK, Dong Z, Cao Y, Zheng Y, Leung TY, Choy KW, Zhu Y
Prenat Diagn. 2024 Nov;44(12):1451-1461
4
Thalassemia screening by third-generation sequencing: Pilot study in a Thai population
Traisrisilp K, Zheng Y, Choy KW, Chareonkwan P
Obstet Med. 2024 Jun;17(2):101-107
5
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene
Zheng Y, Wong L, Kwan AHW, Dong Z, Kwok KY, Choy KW, Dai H, Cao Y
Prenat Diagn. 2024 Feb;44(2):247-250
6
Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects
Cao Y, Chau MHK, Zheng Y, Zhao Y, Kwan AHW, Hui SYA, Lam YH, Tan TYT, Tse WT, Wong L, Leung TY, Dong Z, Choy KW
Prenat Diagn. 2022 Jun;42(7):862-872. (Impact factor (2022): 3.0, citations: 6
7
Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals
Zheng Y, Zhu B, Tan J, Guan Y, The Chinese Genomic Structural Variants Consortium, Morton CC, Lu G
Diagnostics 2022 Apr, 12(5), 1098
8
Clinical Implementation of Expanded Carrier Screening in Pregnant Women at Early Gestational Weeks: A Chinese Cohort Study
Shi M, Liauw AL, Tong S, Zheng Y, Leung TY, Chong SC, Cao Y, Lau TK, Choy KW, Chung JPW.
Genes (Basel). 2021 Mar 29;12(4):496