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1
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.全基因组无创产前检测发现的额外结果的临床影响：TRIDENT-2研究的随访结果
Am J Hum Genet. 2022 Jul 7;109(7):1344. doi: 10.1016/j.ajhg.2022.06.003.
2
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.全基因组无创性产前检测发现的附加结果的临床影响：TRIDENT-2 研究的随访结果。
Am J Hum Genet. 2022 Jun 2;109(6):1140-1152. doi: 10.1016/j.ajhg.2022.04.018.
3
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.TRIDENT-2：荷兰全国范围内实施全基因组非侵入性产前筛查作为一级筛查检测。
Am J Hum Genet. 2019 Dec 5;105(6):1091-1101. doi: 10.1016/j.ajhg.2019.10.005. Epub 2019 Nov 7.
4
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.荷兰实验室对无创产前检测进行评估的试验。第一部分——临床影响。
Prenat Diagn. 2016 Dec;36(12):1083-1090. doi: 10.1002/pd.4945. Epub 2016 Nov 15.
5
Genome-wide non-invasive prenatal testing in single- and multiple-pregnancies at any risk: Identification of maternal polymorphisms to reduce the number of unnecessary invasive confirmation testing.在任何风险下的单胎和多胎妊娠中的全基因组非侵入性产前检测：鉴定母体多态性以减少不必要的侵入性确认检测数量。
Eur J Obstet Gynecol Reprod Biol. 2020 Sep;252:19-29. doi: 10.1016/j.ejogrb.2020.05.070. Epub 2020 Jun 2.
6
Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.超声异常妊娠中非侵入性产前检测的临床应用价值
Ultrasound Obstet Gynecol. 2017 Jun;49(6):721-728. doi: 10.1002/uog.17228.
7
Uptake of fetal aneuploidy screening after the introduction of the non-invasive prenatal test: A national population-based register study.非侵入性产前检测引入后胎儿非整倍体筛查的应用：一项全国基于人群的登记研究。
Acta Obstet Gynecol Scand. 2021 Jul;100(7):1265-1272. doi: 10.1111/aogs.14091. Epub 2021 Feb 9.
8
Analysis of the accuracy of Z-scores of non-invasive prenatal testing for fetal Trisomies 13, 18, and 21 that employs the ion proton semiconductor sequencing platform.采用离子质子半导体测序平台的胎儿13、18和21三体非侵入性产前检测Z值准确性分析。
Mol Cytogenet. 2018 Aug 25;11:49. doi: 10.1186/s13039-018-0397-x. eCollection 2018.
9
Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions.在国家医疗体系中实施非侵入性产前基因检测以筛查染色体非整倍体：全球挑战与国家解决方案
BMC Health Serv Res. 2017 Sep 19;17(1):670. doi: 10.1186/s12913-017-2618-0.
10
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.荷兰实验室对无创产前检测进行评估的试验。第二部分——女性视角。
Prenat Diagn. 2016 Dec;36(12):1091-1098. doi: 10.1002/pd.4941. Epub 2016 Nov 16.

引用本文的文献

1
Analysis of prenatal diagnosis and pregnancy outcomes for rare autosomal trisomies detected by non-invasive prenatal testing in 33,079 cases.33079例无创产前检测检出的罕见常染色体三体的产前诊断及妊娠结局分析
BMC Med Genomics. 2025 Feb 7;18(1):29. doi: 10.1186/s12920-025-02099-3.
2
Performance of Massive Parallel Sequencing-Based Cell-Free DNA Testing in Compromised Pregnancies.基于大规模平行测序的游离DNA检测在高危妊娠中的应用
J Clin Med. 2024 Jul 9;13(14):4007. doi: 10.3390/jcm13144007.
3
Rare autosomal trisomies detected by non-invasive prenatal testing.通过无创产前检测发现的罕见常染色体三体性疾病。
Eur J Hum Genet. 2022 Dec;30(12):1318-1319. doi: 10.1038/s41431-022-01174-y. Epub 2022 Aug 31.

Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.

作者信息

van Prooyen Schuurman Lisanne, Sistermans Erik A, Van Opstal Diane, Henneman Lidewij, Bekker Mireille N, Bax Caroline J, Pieters Mijntje J, Bouman Katelijne, de Munnik Sonja, den Hollander Nicolette S, Diderich Karin E M, Faas Brigitte H W, Feenstra Ilse, Go Attie T J I, Hoffer Mariëtte J V, Joosten Marieke, Komdeur Fenne L, Lichtenbelt Klaske D, Lombardi Maria P, Polak Marike G, Jehee Fernanda S, Schuring-Blom Heleen, Stevens Servi J C, Srebniak Malgorzata I, Suijkerbuijk Ron F, Tan-Sindhunata Gita M, van der Meij Karuna R M, van Maarle Merel C, Vernimmen Vivian, van Zelderen-Bhola Shama L, van Ravesteyn Nicolien T, Knapen Maarten F C M, Macville Merryn V E, Galjaard Robert-Jan H

出版信息

Am J Hum Genet. 2022 Jul 7;109(7):1344. doi: 10.1016/j.ajhg.2022.06.003.

DOI:10.1016/j.ajhg.2022.06.003
PMID:35803237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9300874/
Abstract
摘要