BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

324 related articles for article (PubMed ID: 31439719)

  • 1. Long-read sequencing and haplotype linkage analysis enabled preimplantation genetic testing for patients carrying pathogenic inversions.
    Zhang S; Liang F; Lei C; Wu J; Fu J; Yang Q; Luo X; Yu G; Wang D; Zhang Y; Lu D; Sun X; Liang Y; Xu C
    J Med Genet; 2019 Nov; 56(11):741-749. PubMed ID: 31439719
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis.
    Pei Z; Deng K; Lei C; Du D; Yu G; Sun X; Xu C; Zhang S
    Front Genet; 2021; 12():810900. PubMed ID: 35116057
    [No Abstract]   [Full Text] [Related]  

  • 3. GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction.
    De Witte L; Raman L; Baetens M; De Koker A; Callewaert N; Symoens S; Tilleman K; Vanden Meerschaut F; Dheedene A; Menten B
    Hum Reprod; 2022 Jun; 37(7):1678-1691. PubMed ID: 35552408
    [TBL] [Abstract][Full Text] [Related]  

  • 4. BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers.
    Zhang S; Zhao D; Zhang J; Mao Y; Kong L; Zhang Y; Liang B; Sun X; Xu C
    BMC Med Genomics; 2019 Mar; 12(1):52. PubMed ID: 30885195
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.
    Yuan P; Xia J; Ou S; Liu P; Du T; Zheng L; Yin X; Xie L; Zhang S; Yan H; Gao Y; Zhang Q; Jiang H; Chen F; Wang W
    J Assist Reprod Genet; 2020 Oct; 37(10):2525-2533. PubMed ID: 32783137
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing.
    Tsuiko O; El Ayeb Y; Jatsenko T; Allemeersch J; Melotte C; Ding J; Debrock S; Peeraer K; Vanhie A; De Leener A; Pirard C; Kluyskens C; Denayer E; Legius E; Vermeesch JR; Brems H; Dimitriadou E
    Hum Reprod; 2023 Mar; 38(3):511-519. PubMed ID: 36625546
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
    Xie P; Hu X; Kong L; Mao Y; Cheng D; Kang K; Dai J; Zhao D; Zhang Y; Lu N; Wan Z; Du R; Xiong B; Zhang J; Tan Y; Lu G; Gong F; Lin G; Liang B; Du J; Hu L
    Hum Reprod; 2022 Oct; 37(11):2546-2559. PubMed ID: 36066440
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of Preimplantation and Clinical Outcomes of Two Cases by Oxford Nanopore Sequencing.
    Ou J; Wang J; Sun J; Ni M; Meng Q; Ding J; Fan H; Feng S; Huang Y; Li H; Fei J
    Reprod Sci; 2024 Feb; ():. PubMed ID: 38347380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencing.
    Yuan P; Zheng L; Ou S; Zhao H; Li R; Luo H; Tan X; Zhang Q; Wang W
    J Assist Reprod Genet; 2021 Mar; 38(3):709-718. PubMed ID: 33409753
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives.
    Li Q; Mao Y; Li S; Du H; He W; He J; Kong L; Zhang J; Liang B; Liu J
    BMC Med Genomics; 2020 Aug; 13(1):117. PubMed ID: 32819358
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A comprehensive and universal approach for embryo testing in patients with different genetic disorders.
    Zhang S; Lei C; Wu J; Xiao M; Zhou J; Zhu S; Fu J; Lu D; Sun X; Xu C
    Clin Transl Med; 2021 Jul; 11(7):e490. PubMed ID: 34323405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing.
    Masset H; Zamani Esteki M; Dimitriadou E; Dreesen J; Debrock S; Derhaag J; Derks K; Destouni A; Drüsedau M; Meekels J; Melotte C; Peeraer K; Tšuiko O; van Uum C; Allemeersch J; Devogelaere B; François KO; Happe S; Lorson D; Richards RL; Theuns J; Brunner H; de Die-Smulders C; Voet T; Paulussen A; Coonen E; Vermeesch JR
    Hum Reprod; 2019 Aug; 34(8):1608-1619. PubMed ID: 31348829
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical application of next generation sequencing-based haplotype linkage analysis in the preimplantation genetic testing for germline mosaicisms.
    Chen D; Xu Y; Fu Y; Wang Y; Liu Y; Ding C; Cai B; Pan J; Wang J; Li R; Guo J; Zhang H; Zeng Y; Shen X; Zhou C
    Orphanet J Rare Dis; 2023 Jun; 18(1):137. PubMed ID: 37270548
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers.
    Zhang S; Lei C; Wu J; Zhou J; Sun H; Fu J; Sun Y; Sun X; Lu D; Zhang Y
    BMC Med Genomics; 2017 Oct; 10(1):60. PubMed ID: 29041973
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of carrier status of Xp22.31 microdeletions associated with X-linked ichthyosis at the single-cell level using haplotype linkage analysis by karyomapping.
    Yang J; Shi H; Niu W; Bao X; Liu H; Chen C; Jin H; Song W; Sun Y
    J Assist Reprod Genet; 2023 Jul; 40(7):1735-1746. PubMed ID: 37154837
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Long-read sequencing on the SMRT platform enables efficient haplotype linkage analysis in preimplantation genetic testing for β-thalassemia.
    Wu H; Chen D; Zhao Q; Shen X; Liao Y; Li P; Chiu PCN; Zhou C
    J Assist Reprod Genet; 2022 Mar; 39(3):739-746. PubMed ID: 35141813
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform.
    Hu L; Liang F; Cheng D; Zhang Z; Yu G; Zha J; Wang Y; Xia Q; Yuan D; Tan Y; Wang D; Liang Y; Lin G
    Front Genet; 2019; 10():1313. PubMed ID: 32010185
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a
    Wen X; Du J; Li Z; Liu N; Huo J; Li J; Ke W; Wu J; Fang X; Lin X
    Front Genet; 2023; 14():1169868. PubMed ID: 37779904
    [No Abstract]   [Full Text] [Related]  

  • 19. Infertility patients with chromosome inversions are not susceptible to an inter-chromosomal effect.
    Young D; Klepacka D; McGarvey M; Schoolcraft WB; Katz-Jaffe MG
    J Assist Reprod Genet; 2019 Mar; 36(3):509-516. PubMed ID: 30554392
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts.
    Treff NR; Thompson K; Rafizadeh M; Chow M; Morrison L; Tao X; Garnsey H; Reda CV; Metzgar TL; Neal S; Jalas C; Scott RT; Forman EJ
    J Assist Reprod Genet; 2016 Aug; 33(8):1115-9. PubMed ID: 27241531
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.