292 related articles for article (PubMed ID: 33799648)
1. Optical Genome Mapping as a Next-Generation Cytogenomic Tool for Detection of Structural and Copy Number Variations for Prenatal Genomic Analyses.
Sahajpal NS; Barseghyan H; Kolhe R; Hastie A; Chaubey A
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33799648
[TBL] [Abstract][Full Text] [Related]
2. Optical genome mapping enables constitutional chromosomal aberration detection.
Mantere T; Neveling K; Pebrel-Richard C; Benoist M; van der Zande G; Kater-Baats E; Baatout I; van Beek R; Yammine T; Oorsprong M; Hsoumi F; Olde-Weghuis D; Majdali W; Vermeulen S; Pauper M; Lebbar A; Stevens-Kroef M; Sanlaville D; Dupont JM; Smeets D; Hoischen A; Schluth-Bolard C; El Khattabi L
Am J Hum Genet; 2021 Aug; 108(8):1409-1422. PubMed ID: 34237280
[TBL] [Abstract][Full Text] [Related]
3. Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing.
Sahajpal NS; Mondal AK; Fee T; Hilton B; Layman L; Hastie AR; Chaubey A; DuPont BR; Kolhe R
J Mol Diagn; 2023 Apr; 25(4):234-246. PubMed ID: 36758723
[TBL] [Abstract][Full Text] [Related]
4. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
[TBL] [Abstract][Full Text] [Related]
5. Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinement.
Barseghyan H; Pang AWC; Clifford B; Serrano MA; Chaubey A; Hastie AR
Genes (Basel); 2023 Sep; 14(10):. PubMed ID: 37895217
[TBL] [Abstract][Full Text] [Related]
6. Optical Genome Mapping: A Revolutionary Tool for "Next Generation Cytogenomics Analysis" with a Broad Range of Diagnostic Applications in Human Diseases.
Garcia-Heras J
J Assoc Genet Technol; 2021; 47(4):191-200. PubMed ID: 34897113
[TBL] [Abstract][Full Text] [Related]
7. Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping.
Neveling K; Mantere T; Vermeulen S; Oorsprong M; van Beek R; Kater-Baats E; Pauper M; van der Zande G; Smeets D; Weghuis DO; Stevens-Kroef MJPL; Hoischen A
Am J Hum Genet; 2021 Aug; 108(8):1423-1435. PubMed ID: 34237281
[TBL] [Abstract][Full Text] [Related]
8. Expanding the application of non-invasive prenatal testing in the detection of foetal chromosomal copy number variations.
Wang C; Tang J; Tong K; Huang D; Tu H; Li Q; Zhu J
BMC Med Genomics; 2021 Dec; 14(1):292. PubMed ID: 34895207
[TBL] [Abstract][Full Text] [Related]
9. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
[TBL] [Abstract][Full Text] [Related]
10. Detection of complex chromosome rearrangements using optical genome mapping.
Qu J; Li S; Yu D
Gene; 2023 Oct; 884():147688. PubMed ID: 37543218
[TBL] [Abstract][Full Text] [Related]
11. Optical genome mapping in acute myeloid leukemia: a multicenter evaluation.
Levy B; Baughn LB; Akkari Y; Chartrand S; LaBarge B; Claxton D; Lennon PA; Cujar C; Kolhe R; Kroeger K; Pitel B; Sahajpal N; Sathanoori M; Vlad G; Zhang L; Fang M; Kanagal-Shamanna R; Broach JR
Blood Adv; 2023 Apr; 7(7):1297-1307. PubMed ID: 36417763
[TBL] [Abstract][Full Text] [Related]
12. Analytic Validation of Optical Genome Mapping in Hematological Malignancies.
Pang AWC; Kosco K; Sahajpal NS; Sridhar A; Hauenstein J; Clifford B; Estabrook J; Chitsazan AD; Sahoo T; Iqbal A; Kolhe R; Raca G; Hastie AR; Chaubey A
Biomedicines; 2023 Dec; 11(12):. PubMed ID: 38137484
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication.
Tian W; Yuan Y; Yuan E; Zhang L; Liu L; Li Y; Guo J; Cui X; Li P; Cui S
Eur J Med Res; 2023 Aug; 28(1):304. PubMed ID: 37644576
[TBL] [Abstract][Full Text] [Related]
14. [Report content and prenatal diagnosis of non-invasive prenatal testing for sex chromosome aneuploidy].
Zhou CX; He LL; Zhu XY; Li ZX; Duan HL; Liu W; Gu LL; Li J
Zhonghua Fu Chan Ke Za Zhi; 2023 Oct; 58(10):766-773. PubMed ID: 37849257
[No Abstract] [Full Text] [Related]
15. Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis.
Zhang Q; Wang Y; Xu Y; Zhou R; Huang M; Qiao F; Meng L; Liu A; Zhou J; Li L; Ji X; Xu Z; Hu P
Acta Obstet Gynecol Scand; 2023 Aug; 102(8):1053-1062. PubMed ID: 37366235
[TBL] [Abstract][Full Text] [Related]
16. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
Beulen L; Faas BHW; Feenstra I; van Vugt JMG; Bekker MN
Ultrasound Obstet Gynecol; 2017 Jun; 49(6):721-728. PubMed ID: 27515011
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.
Badeau M; Lindsay C; Blais J; Nshimyumukiza L; Takwoingi Y; Langlois S; Légaré F; Giguère Y; Turgeon AF; Witteman W; Rousseau F
Cochrane Database Syst Rev; 2017 Nov; 11(11):CD011767. PubMed ID: 29125628
[TBL] [Abstract][Full Text] [Related]
19. Optical Genome Mapping in Routine Human Genetic Diagnostics-Its Advantages and Limitations.
Dremsek P; Schwarz T; Weil B; Malashka A; Laccone F; Neesen J
Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946907
[TBL] [Abstract][Full Text] [Related]
20. [The value of non-invasive prenatal testing for the identification of numerical and structural chromosomal abnormalities and copy number variations in the fetuses].
Hou S; Zhang H; Li C; Chen D; Yan H; Yang M; Liu Y; Lei D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Oct; 40(10):1197-1203. PubMed ID: 37730217
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
