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Hilary Bowman-Smart, Christopher Gyngell, Cara Mand, David J. Amor, Martin B. Delatycki & Julian Savulescu. (2023) Non-Invasive Prenatal Testing for “Non-Medical” Traits: Ensuring Consistency in Ethical Decision-Making. The American Journal of Bioethics 23:3, pages 3-20.
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Junhui Wan, Ru Li, Fatao Li, Qiuxia Yu, Dan Wang, Xiuhong Sun, Yongling Zhang, Xiangyi Jing, Xuewei Tang, Guilan Chen, Fan Jiang, Fucheng Li, Fang Fu, Yan Li, Lina Zhang, Cuixing Yi, Jian Li, Dongzhi Li & Can Liao. (2022) Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing. The Journal of Maternal-Fetal & Neonatal Medicine 35:25, pages 9647-9653.
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Li Wen, Jiye Gao, Leilei Huang, Dongmei Li & Guansheng Zhong. (2022) Noninvasive prenatal screening in southeast China: clinical application and accuracy evaluation. Expert Review of Molecular Diagnostics 22:8, pages 841-848.
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Cechuan Deng, Sau Wai Cheung & Hongqian Liu. (2021) Noninvasive prenatal screening for fetal sex chromosome aneuploidies. Expert Review of Molecular Diagnostics 21:4, pages 405-415.
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Yong Xu, Siqi Hu, Liyuan Chen, Ying Hao, Hu Zhang, Zhiyong Xu, Weiqing Wu & Liyanyan Deng. (2023) Application of non-invasive prenatal testing in screening chromosomal aberrations in pregnancies with different nuchal translucency cutoffs. Molecular Cytogenetics 16:1.
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Dongmei Wang, Haishan Peng, Yixia Wang, Yaping Hou, Fangfang Guo, Juan Zhu, Tingting Hu & Jiexia Yang. (2023) Performance of noninvasive prenatal testing for twin pregnancies in South China. Journal of Assisted Reproduction and Genetics.
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Xiying Yuan, Weinan Wang, Lei Dai, Wenjing Yong, Chenlin Pei, Jingzhi Li & Lingqian Wu. (2023) Noninvasive prenatal testing, ultrasonographic findings and poor prenatal diagnosis rates for twin pregnancies: a retrospective study. BMC Pregnancy and Childbirth 23:1.
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Sofia Bussolaro, Yvette C. Raymond, Melissa L. Acreman, Maurizio Guido, Fabricio Da Silva Costa, Daniel L. Rolnik & Ilaria Fantasia. (2023) The accuracy of prenatal cell-free DNA screening for sex chromosome abnormalities: A systematic review and meta-analysis. American Journal of Obstetrics & Gynecology MFM 5:3, pages 100844.
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Ivonne Bedei, Tascha Gehrke, Karl‐Philipp Gloning, Matthias Meyer‐Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai‐Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M. Jahns, Annegret Geipel, Jan‐Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B. Van den Veyver & Roland Axt‐Fliedner. (2023) Multicenter clinical experience with non‐invasive cell‐free DNA screening for monosomy X and related X‐chromosome variants. Prenatal Diagnosis 43:2, pages 192-206.
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Molly Johnston, Chanelle Warton, Mark D. Pertile, Michelle Taylor‐Sands, Martin B. Delatycki, Lisa Hui, Julian Savulescu & Catherine Mills. (2022) Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy. Prenatal Diagnosis 43:2, pages 226-234.
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Xinning Chen, Dan Lin, Yinghui Ye, Xiaohui Zhang & Danqing Chen. (2022) Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014–2020. Orphanet Journal of Rare Diseases 17:1.
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Siping Liu, Fang Yang, Qingxian Chang, Bei Jia, Yushuang Xu, Ruifeng Wu, Liyan Li, Weishan Chen, Ailan Yin, Fodi Huang, Suxin Feng & Fenxia Li. (2022) Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review. Molecular Cytogenetics 15:1.
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Huili Xue, Aili Yu, Min Lin, Xuemei Chen, Qun Guo, Liangpu Xu & Hailong Huang. (2022) Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies. Scientific Reports 12:1.
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Nan Guo, Meiying Cai, Min Lin, Huili Xue, Hailong Huang & Liangpu Xu. (2022) Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities. Molecular Biology Reports 49:10, pages 9251-9256.
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Ganye Zhao, Peng Dai, Conghui Wang, Lina Liu, Xuechao Zhao & Xiangdong Kong. (2022) Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China. Frontiers in Medicine 8.
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Yanmei Lu, Shihao Zhou, Siyuan Linpeng, Siyi Ding, Shihong Li, Yujiao Li, Liangcheng Shi, Jun He & Yalan Liu. (2022) Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018–2020: A Retrospective Analysis. Journal of Personalized Medicine 12:1, pages 48.
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Xinran Lu, Chaohong Wang, Yuxiu Sun, Junxiang Tang, Keting Tong & Jiansheng Zhu. (2021) Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases. Molecular Cytogenetics 14:1.
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Jiexia Yang, Yaping Hou, Fangfang Guo, Haishan Peng, Dongmei Wang, Yi Li, Haoxin OY, Yixia Wang, Jian Lu & Aihua Yin. (2021) Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China. Journal of Assisted Reproduction and Genetics 38:3, pages 727-734.
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Yunfang Shi, Xiaozhou Li, Duan Ju, Yan Li, Xiuling Zhang & Ying Zhang. (2021) Efficiency of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies. Gynecologic and Obstetric Investigation 86:4, pages 379-387.
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Xiaoqing Wu, Ying Li, Xiaorui Xie, Linjuan Su, Meiying Cai, Na Lin, Shengrong Du, Liangpu Xu & Hailong Huang. (2020) Clinical Review of Noninvasive Prenatal Testing. The Journal of Molecular Diagnostics 22:12, pages 1469-1475.
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Xiaolei Xie, Weihe Tan, Fuguang Li, Eric Carrano, Paola Ramirez, Autumn DiAdamo, Brittany Grommisch, Katherine Amato, Hongyan Chai, Jiadi Wen & Peining Li. (2020) Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence. Molecular Genetics & Genomic Medicine 8:7.
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Ganye Zhao, Peng Dai, Shanshan Gao, Xuechao Zhao, Conghui Wang, Lina Liu & Xiangdong Kong. (2019) A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing. Molecular Cytogenetics 12:1.
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Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Fang Xu, Qinghua Zhou, Jiadi Wen, Maurice Mahoney, Allen Bale, James McGrath, Michele Spencer-Manzon, Peining Li & Hui Zhang. (2019) A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings. Frontiers in Genetics 10.
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