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443 related items for PubMed ID: 34913786

  • 21. Noninvasive preimplantation genetic testing for aneuploidy in spent medium may be more reliable than trophectoderm biopsy.
    Huang L, Bogale B, Tang Y, Lu S, Xie XS, Racowsky C.
    Proc Natl Acad Sci U S A; 2019 Jul 09; 116(28):14105-14112. PubMed ID: 31235575
    [Abstract] [Full Text] [Related]

  • 22. Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure.
    Del Rey J, Vidal F, Ramírez L, Borràs N, Corrales I, Garcia I, Martinez-Pasarell O, Fernandez SF, Garcia-Cruz R, Pujol A, Plaja A, Salaverria I, Oliver-Bonet M, Benet J, Navarro J.
    PLoS One; 2018 Jul 09; 13(10):e0205692. PubMed ID: 30332465
    [Abstract] [Full Text] [Related]

  • 23. Preimplantation Genetic Testing for Rare Inherited Disease of MMA-CblC: an Unaffected Live Birth.
    Peng C, Ren J, Li Y, Keqie Y, Zhou F, Zhang X, Zhu H, Hu T, Wang H, Chen X, Liu S.
    Reprod Sci; 2021 Dec 09; 28(12):3571-3578. PubMed ID: 34076870
    [Abstract] [Full Text] [Related]

  • 24. Next-Generation Sequencing (NGS)-Based Preimplantation Genetic Testing for Aneuploidy (PGT-A) of Trophectoderm Biopsy for Recurrent Implantation Failure (RIF) Patients: a Retrospective Study.
    Tong J, Niu Y, Wan A, Zhang T.
    Reprod Sci; 2021 Jul 09; 28(7):1923-1929. PubMed ID: 33709375
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 38(3):511-519. PubMed ID: 36625546
    [Abstract] [Full Text] [Related]

  • 26. The clinical application of NGS-based SNP haplotyping for PGD of Hb H disease.
    Chen L, Diao Z, Xu Z, Zhou J, Yan G, Sun H.
    Syst Biol Reprod Med; 2017 Jun 01; 63(3):212-217. PubMed ID: 28340305
    [Abstract] [Full Text] [Related]

  • 27. The reproducibility of trophectoderm biopsies in euploid, aneuploid, and mosaic embryos using independently verified next-generation sequencing (NGS): a pilot study.
    Sachdev NM, McCulloh DH, Kramer Y, Keefe D, Grifo JA.
    J Assist Reprod Genet; 2020 Mar 01; 37(3):559-571. PubMed ID: 32112203
    [Abstract] [Full Text] [Related]

  • 28. The true incidence of chromosomal mosaicism after preimplantation genetic testing is much lower than that indicated by trophectoderm biopsy.
    Wu L, Jin L, Chen W, Liu JM, Hu J, Yu Q, Ren XL, Huang B, He H.
    Hum Reprod; 2021 May 17; 36(6):1691-1701. PubMed ID: 33860322
    [Abstract] [Full Text] [Related]

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  • 30. 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 17; 37(10):2525-2533. PubMed ID: 32783137
    [Abstract] [Full Text] [Related]

  • 31. Preimplantation genetic testing for Aicardi-Goutières syndrome induced by novel compound heterozygous mutations of TREX1: an unaffected live birth.
    Xu H, Pu J, Lin S, Hu R, Yao J, Li X.
    Mol Cytogenet; 2023 Jun 05; 16(1):9. PubMed ID: 37277873
    [Abstract] [Full Text] [Related]

  • 32. Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemma.
    Popovic M, Dhaenens L, Boel A, Menten B, Heindryckx B.
    Hum Reprod Update; 2020 Apr 15; 26(3):313-334. PubMed ID: 32141501
    [Abstract] [Full Text] [Related]

  • 33. Successful four-factor preimplantation genetic testing: α- and β-thalassemia, human leukocyte antigen typing, and aneuploidy screening.
    Chen D, Shen X, Xu Y, Ding C, Ye Q, Zhong Y, Xu Y, Zhou C.
    Syst Biol Reprod Med; 2021 Apr 15; 67(2):151-159. PubMed ID: 33494632
    [Abstract] [Full Text] [Related]

  • 34. Extended in vitro culture of human embryos demonstrates the complex nature of diagnosing chromosomal mosaicism from a single trophectoderm biopsy.
    Popovic M, Dhaenens L, Taelman J, Dheedene A, Bialecka M, De Sutter P, Chuva de Sousa Lopes SM, Menten B, Heindryckx B.
    Hum Reprod; 2019 Apr 01; 34(4):758-769. PubMed ID: 30838420
    [Abstract] [Full Text] [Related]

  • 35. Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism.
    Hu X, He WB, Zhang SP, Luo KL, Gong F, Dai J, Zhang Y, Wan ZX, Li W, Yuan SM, Tan YQ, Lu GX, Lin G, Du J.
    Mol Genet Genomic Med; 2021 May 01; 9(5):e1662. PubMed ID: 33942572
    [Abstract] [Full Text] [Related]

  • 36. Noninvasive preimplantation genetic testing for aneuploidy exhibits high rates of deoxyribonucleic acid amplification failure and poor correlation with results obtained using trophectoderm biopsy.
    Hanson BM, Tao X, Hong KH, Comito CE, Pangasnan R, Seli E, Jalas C, Scott RT.
    Fertil Steril; 2021 Jun 01; 115(6):1461-1470. PubMed ID: 33745720
    [Abstract] [Full Text] [Related]

  • 37. Universal strategy for preimplantation genetic testing for cystic fibrosis based on next generation sequencing.
    Chamayou S, Sicali M, Lombardo D, Alecci C, Ragolia C, Maglia E, Liprino A, Cardea C, Storaci G, Romano S, Guglielmino A.
    J Assist Reprod Genet; 2020 Jan 01; 37(1):213-222. PubMed ID: 31828483
    [Abstract] [Full Text] [Related]

  • 38. Proband-independent haplotyping based on NGS-based long-read sequencing for detecting pathogenic variant carrier status in preimplantation genetic testing for monogenic diseases.
    Zhang P, Zhao X, Li Q, Xu Y, Cheng Z, Yang L, Wang H, Tao Y, Huang G, Wu R, Zhou H, Zhao S.
    Front Mol Biosci; 2024 Jan 01; 11():1329580. PubMed ID: 38516188
    [Abstract] [Full Text] [Related]

  • 39. Evaluating the application value of NGS-based PGT-A by screening cryopreserved MDA products of embryos from PGT-M cycles with known transfer outcomes.
    Shen X, Chen D, Ding C, Xu Y, Fu Y, Cai B, Wang Y, Wang J, Li R, Guo J, Pan J, Zhang H, Zeng Y, Zhou C.
    J Assist Reprod Genet; 2022 Jun 01; 39(6):1323-1331. PubMed ID: 35275308
    [Abstract] [Full Text] [Related]

  • 40. 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 20; 13(1):117. PubMed ID: 32819358
    [Abstract] [Full Text] [Related]

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