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8th
王元麗,唐明珠,楊學習. 11339例孕婦無創產前檢測結果對比分析. 分子診斷與治療雜志[J],2016,8(6),363-366.
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7th
許旭平,謝美娟,甘海燕,梁榮良,韓爾康,楊學習,吳英松. 基于高通量測序技術無創篩查雙胎染色體非整倍體及胎兒游離DNA濃度分析.分子診斷與治療雜志[J],2016,8(6),375-379.
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6th
Mei-Juan Xie, Zhi-kun Liang, et al. Noninvasive Prenatal Testing of Rare Autosomal Aneuploidies by Semiconductor Sequencing.DNA Cell Biol. 2018 Mar;37(3):174-181.
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5th
Xu-Ping Xu, Hai-Yan Gan, Fen-Xia Li, Qi Tian, Jun Zhang, Rong-Liang Liang, Ming Li, Xue-Xi Yang , Ying-Song Wu. PLOS ONE 2016,10.A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection
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4th
Sun K, Jiang P, Wong A I, et al. Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing[J]. Proceedings of the National Academy of Sciences of the United States of America, 2018, 115(22).
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3th
Chan KCA, et al. (2016) Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends. Proc Natl Acad Sci USA 113:E8159–E8168.
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2th
Lo YMD, et al. (2010) Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Sci Transl Med 2:61ra91.
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1th
van Opstal D, et al. (2018) Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: Results of the TRIDENT study. Genet Med 20:480–485.
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