| Issue Date | Title | Author(s) |
| 2023 | Application of the PGT-M strategy using single sperm and/or affected embryos as probands for linkage analysis in males with hereditary tumor syndromes without family history | Chen, Xi; Wang, Yuqian; Guan, Shuo; Yan, Zhiqiang; Zhu, Xiaohui; Kuo, Ying; Wang, Nan; Zhi, Xu; Lian, Ying; Huang, Jin; Liu, Ping; Li, Rong; Yan, Liying; Qiao, Jie |
| Mar-2021 | Clinical application of an NGS-based method in the preimplantation genetic testing for Duchenne muscular dystrophy | Ren, Yixin; Lian, Ying; Yan, Zhiqiang; Zhai, Fan; Yang, Ming; Zhu, Xiaohui; Wang, Yuqian; Nie, Yanli; Guan, Shuo; Kuo, Ying; Huang, Jin; Shi, Xiaodan; Jia, Jialin; Qiao, Jie; Yan, Liying |
| 13-Nov-2023 | Clinical practice and outcomes of preimplantation genetic testing for CMT1A using a novel direct detection method | Wang, Yuqian; Liu, Yujun; Kuo, Ying; Guan, Shuo; Wang, Nan; Lian, Ying; Huang, Jin; Zhi, Xu; Liu, Ping; Li, Rong; Yan, Liying; Zhu, Xiaohui; Qiao, Jie |
| May-2021 | A comprehensive PGT-M strategy for ADPKD patients with de novo PKD1 mutations using affected embryo or gametes as proband | Wang, Yuqian; Zhai, Fan; Guan, Shuo; Yan, Zhiqiang; Zhu, Xiaohui; Kuo, Ying; Wang, Nan; Zhi, Xu; Lian, Ying; Huang, Jin; Jia, Jialin; Liu, Ping; Li, Rong; Qiao, Jie; Yan, Liying |
| 2023 | A novel embryo biopsy morphological analysis and genetic integrality criterion system significantly improves the outcome of preimplantation genetic testing | Kuo, Ying; Zhu, Xiaohui; Guo, Qianying; Wang, Yuqian; Guan, Shuo; Liu, Ping; Li, Rong; Yan, Zhiqiang; Yan, Liying; Qiao, Jie |
| Apr-2020 | Novel PGD strategy based on single sperm linkage analysis for carriers of single gene pathogenic variant and chromosome reciprocal translocation | Wang, Yuqian; Zhu, Xiaohui; Yan, Zhiqiang; Zhi, Xu; Guan, Shuo; Kuo, Ying; Nie, Yanli; Lian, Ying; Huang, Jin; Wei, Yuan; Liu, Ping; Li, Rong; Qiao, Jie; Yan, Liying |
| Sep-2022 | Preimplantation genetic testing for structural rearrangement based on low-coverage next-generation sequencing accurately discriminates between normal and carrier embryos for patients with translocations | Zhai, Fan; Wang, Yun; Li, Hanna; Wang, Yuqian; Zhu, Xiaohui; Kuo, Ying; Guan, Shuo; Li, Jiacheng; Song, Shi; He, Qilong; An, Jianting; Zhi, Xu; Lian, Ying; Huang, Jin; Li, Rong; Qiao, Jie; Yan, Liying; Yan, Zhiqiang |
| 1-Feb-2020 | scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data | Yan, Zhiqiang; Zhu, Xiaohui; Wang, Yuqian; Nie, Yanli; Guan, Shuo; Kuo, Ying; Chang, Di; Li, Rong; Qiao, Jie; Yan, Liying |
| May-2020 | A strategy using SNP linkage analysis for monogenic diseases PGD combined with HLA typing | Wang, Yuqian; Qin, Meng; Yan, Zhiqiang; Guan, Shuo; Kuo, Ying; Kong, Siming; Nie, Yanli; Zhu, Xiaohui; Zhi, Xu; Qiao, Jie; Yan, Liying |
| Feb-2020 | Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations | Guo, Wei; Lai, Yuchen; Yan, Zhiqiang; Wang, Yuqian; Nie, Yanli; Guan, Shuo; Kuo, Ying; Zhang, Wenxin; Zhu, Xiaohui; Peng, Mei; Zhi, Xu; Wei, Yuan; Yan, Liying; Qiao, Jie |
