133 related articles for article (PubMed ID: 38448011)
1. [Application of optical genome mapping technology for the detection of chromosomal structural variations].
Zhang Z; He S; Li X; Cheng K; Wei Y; Ren Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Mar; 41(3):257-265. PubMed ID: 38448011
[TBL] [Abstract][Full Text] [Related]
2. Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping.
Zhang S; Pei Z; Lei C; Zhu S; Deng K; Zhou J; Yang J; Lu D; Sun X; Xu C; Xu C
J Med Genet; 2023 Mar; 60(3):274-284. PubMed ID: 35710108
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Efficacy and initial clinical evaluation of optical genome mapping in the diagnosis of structural variations].
Hao N; Zhou J; Li MM; Luo WW; Zhang HZ; Qi QW; Jiang YL; Zhou XY; Yang K; Chen H; Pan HJ; Zhu JT; Liu J
Zhonghua Yu Fang Yi Xue Za Zhi; 2022 May; 56(5):632-639. PubMed ID: 35644979
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of optical genome mapping for detecting chromosomal translocation in clinical cytogenetics.
Dai P; Zhu X; Pei Y; Chen P; Li J; Gao Z; Liang Y; Kong X
Mol Genet Genomic Med; 2022 Jun; 10(6):e1936. PubMed ID: 35384386
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Analysis of chromosomal structural variations in patients with recurrent spontaneous abortion using optical genome mapping.
Rao H; Zhang H; Zou Y; Ma P; Huang T; Yuan H; Zhou J; Lu W; Li Q; Huang S; Liu Y; Yang B
Front Genet; 2023; 14():1248755. PubMed ID: 37732322
[No Abstract] [Full Text] [Related]
8. [Optical genome mapping analysis of a Chinese pedigree with a rare chromosome 17 paracentric inversion insertion].
Wang H; Yang Y; Yang N; Wang Y; Li H; Hu W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):727-732. PubMed ID: 37212011
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Optical Genome Mapping for Chromosomal Aberrations Detection-False-Negative Results and Contributing Factors.
Xu Y; Zhang Q; Wang Y; Zhou R; Ji X; Meng L; Luo C; Liu A; Jiao J; Chen H; Zeng H; Hu P; Xu Z
Diagnostics (Basel); 2024 Jan; 14(2):. PubMed ID: 38248042
[TBL] [Abstract][Full Text] [Related]
11. Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation.
Ogiwara Y; Hattori A; Ikegawa K; Hasegawa Y; Kuroki Y; Miyado M; Fukami M
Cytogenet Genome Res; 2022; 162(11-12):617-624. PubMed ID: 37231804
[TBL] [Abstract][Full Text] [Related]
12. Identification of complex and cryptic chromosomal rearrangements by optical genome mapping.
Shi S; Huang P; Yan R; Li R
Mol Cytogenet; 2023 Apr; 16(1):5. PubMed ID: 37101225
[TBL] [Abstract][Full Text] [Related]
13. Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL.
Vieler LM; Nilius-Eliliwi V; Schroers R; Vangala DB; Nguyen HP; Gerding WM
Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980958
[TBL] [Abstract][Full Text] [Related]
14. 11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation.
Zhang Q; Wang Y; Zhou J; Zhou R; Liu A; Meng L; Ji X; Hu P; Xu Z
Mol Genet Genomic Med; 2023 Oct; 11(10):e2248. PubMed ID: 37475652
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Two balanced and novel chromosomal translocations in myeloid malignancies. characterization by multiplex fluorescence in situ hybridization.
Wan TS; Ma SK; Yip SF; Yeung YM; Chan LC
Cancer Genet Cytogenet; 2002 Nov; 139(1):52-6. PubMed ID: 12547159
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. OGM and WES identifies translocation breakpoints in PKD1 gene in an polycystic kidney patient and healthy baby delivered using PGT.
Xu P; Wang L; Li J; Huang S; Gao M; Kang R; Li J; Xie H; Liu X; Yan J; Gao X; Gao Y
BMC Med Genomics; 2023 Nov; 16(1):285. PubMed ID: 37953234
[TBL] [Abstract][Full Text] [Related]
19. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.
Liang D; Wang Y; Ji X; Hu H; Zhang J; Meng L; Lin Y; Ma D; Jiang T; Jiang H; Asan ; Song L; Guo J; Hu P; Xu Z
Clin Genet; 2017 Apr; 91(4):605-610. PubMed ID: 27491356
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
