388 related articles for article (PubMed ID: 32539871)
1. Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre study.
Mesoraca A; Margiotti K; Dello Russo C; Cesta A; Cima A; Longo SA; Barone MA; Viola A; Sparacino D; Giorlandino C
Genet Res (Camb); 2020 Jun; 102():e5. PubMed ID: 32539871
[TBL] [Abstract][Full Text] [Related]
2. Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China.
Liu Y; Liu H; He Y; Xu W; Ma Q; He Y; Lei W; Chen G; He Z; Huang J; Liu J; Liu Y; Huang Q; Yu F
Hum Genomics; 2020 Jun; 14(1):21. PubMed ID: 32503639
[TBL] [Abstract][Full Text] [Related]
3. Clinical Validation of Non-Invasive Prenatal Testing for Fetal Common Aneuploidies in 1,055 Korean Pregnant Women: a Single Center Experience.
Lee DE; Kim H; Park J; Yun T; Park DY; Kim M; Ryu HM
J Korean Med Sci; 2019 Jun; 34(24):e172. PubMed ID: 31222985
[TBL] [Abstract][Full Text] [Related]
4. Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.
Hu H; Wang L; Wu J; Zhou P; Fu J; Sun J; Cai W; Liu H; Yang Y
Hum Genomics; 2019 Mar; 13(1):14. PubMed ID: 30871627
[TBL] [Abstract][Full Text] [Related]
5. [Retrospective analysis of cell-free fetal DNA prenatal testing of maternal peripheral blood].
Wei Y; Wang R; Xi M; Wei L; Zhu W; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):933-938. PubMed ID: 37532491
[TBL] [Abstract][Full Text] [Related]
6. TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
van der Meij KRM; Sistermans EA; Macville MVE; Stevens SJC; Bax CJ; Bekker MN; Bilardo CM; Boon EMJ; Boter M; Diderich KEM; de Die-Smulders CEM; Duin LK; Faas BHW; Feenstra I; Haak MC; Hoffer MJV; den Hollander NS; Hollink IHIM; Jehee FS; Knapen MFCM; Kooper AJA; van Langen IM; Lichtenbelt KD; Linskens IH; van Maarle MC; Oepkes D; Pieters MJ; Schuring-Blom GH; Sikkel E; Sikkema-Raddatz B; Smeets DFCM; Srebniak MI; Suijkerbuijk RF; Tan-Sindhunata GM; van der Ven AJEM; van Zelderen-Bhola SL; Henneman L; Galjaard RH; Van Opstal D; Weiss MM;
Am J Hum Genet; 2019 Dec; 105(6):1091-1101. PubMed ID: 31708118
[TBL] [Abstract][Full Text] [Related]
7. Targeted fetal cell-free DNA screening for aneuploidies in 4,594 pregnancies: Single center study.
Koc A; Ozer Kaya O; Ozyilmaz B; Kutbay YB; Kirbiyik O; Ozdemir TR; Erdogan KM; Saka Guvenc M; Oztekin DC; Ozeren M; Pala HG; Ekin A; Gezer C; Sahingoz Yildirim AG; Konuralp Atakul B; Kurtulmus S; Turhan U; Taner CE
Mol Genet Genomic Med; 2019 Jul; 7(7):e00678. PubMed ID: 31070015
[TBL] [Abstract][Full Text] [Related]
8. Assessment and Clinical Utility of a Non-Next-Generation Sequencing-Based Non-Invasive Prenatal Testing Technology.
Gormus U; Chaubey A; Shenoy S; Wong YW; Chan LY; Choo BP; Oraha L; Gousseva A; Persson F; Prensky L; Chin E; Hegde M
Curr Issues Mol Biol; 2021 Aug; 43(2):958-964. PubMed ID: 34449543
[No Abstract] [Full Text] [Related]
9. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Petersen AK; Cheung SW; Smith JL; Bi W; Ward PA; Peacock S; Braxton A; Van Den Veyver IB; Breman AM
Am J Obstet Gynecol; 2017 Dec; 217(6):691.e1-691.e6. PubMed ID: 29032050
[TBL] [Abstract][Full Text] [Related]
10. Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experience.
Margiotti K; Cesta A; Dello Russo C; Cima A; Barone MA; Viola A; Sparacino D; Mesoraca A; Giorlandino C
BMC Res Notes; 2020 Mar; 13(1):167. PubMed ID: 32188487
[TBL] [Abstract][Full Text] [Related]
11. Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit.
Togneri FS; Allen SK; Mann K; Holgado E; Morgan S
Genet Res (Camb); 2020 Sep; 102():e7. PubMed ID: 32867862
[TBL] [Abstract][Full Text] [Related]
12. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW
Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
Junhui W; Ru L; Qiuxia Y; Dan W; Xiuhong S; Yongling Z; Xiangyi J; Fatao L; Xuewei T; Guilan C; Fan J; Fucheng L; Fang F; Yan L; Lina Z; Cuixing Y; Jian L; Dongzhi L; Can L
Prenat Diagn; 2021 May; 41(6):690-696. PubMed ID: 33480032
[TBL] [Abstract][Full Text] [Related]
14. The performance of grey zone in common foetal aneuploidy screening by semiconductor sequencing.
Zhang C; He Q; Qiao L; Li H; Wang T
J Obstet Gynaecol; 2022 Aug; 42(6):1782-1787. PubMed ID: 35465819
[TBL] [Abstract][Full Text] [Related]
15. Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.
Health Quality Ontario
Ont Health Technol Assess Ser; 2019; 19(4):1-166. PubMed ID: 30847010
[TBL] [Abstract][Full Text] [Related]
16. [Clinical significance of non-invasive prenatal testing in preventing birth defects].
Zhang W; Li S; Tang P; Wang J; Gu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1061-1064. PubMed ID: 32924101
[TBL] [Abstract][Full Text] [Related]
17. Screening of fetal chromosomal aneuploidy diseases using noninvasive prenatal testing in twin pregnancies.
Yu W; Lv Y; Yin S; Liu H; Li X; Liang B; Kong L; Liu C
Expert Rev Mol Diagn; 2019 Feb; 19(2):189-196. PubMed ID: 30582381
[TBL] [Abstract][Full Text] [Related]
18. Analysis of cell-free DNA in a consecutive series of 13,607 routine cases for the detection of fetal chromosomal aneuploidies in a single center in Germany.
Borth H; Teubert A; Glaubitz R; Knippenberg S; Kutur N; Winkler T; Eiben B
Arch Gynecol Obstet; 2021 Jun; 303(6):1407-1414. PubMed ID: 33151425
[TBL] [Abstract][Full Text] [Related]
19. Massively Parallel Sequencing (MPS) of Cell-Free Fetal DNA (cffDNA) for Trisomies 21, 18, and 13 in Twin Pregnancies.
Du E; Feng C; Cao Y; Yao Y; Lu J; Zhang Y
Twin Res Hum Genet; 2017 Jun; 20(3):242-249. PubMed ID: 28485265
[TBL] [Abstract][Full Text] [Related]
20. Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting.
El Khattabi LA; Brun S; Gueguen P; Chatron N; Guichoux E; Schutz S; Nectoux J; Sorlin A; Quere M; Boudjarane J; Tsatsaris V; Mandelbrot L; Schluth-Bolard C; Dupont JM; Rooryck C;
Ultrasound Obstet Gynecol; 2019 Aug; 54(2):246-254. PubMed ID: 30191619
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
