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Page 1
Identifying parental and cell-division origins of aneuploidy in the human blastocyst.
Am J Hum Genet. 2023 Apr 6;110(4):565-574. doi: 10.1016/j.ajhg.2023.03.003. Epub 2023 Mar 27.
Am J Hum Genet. 2023.
PMID: 36977411
Free PMC article.
Allele-Specific Chromosome Removal after Cas9 Cleavage in Human Embryos.
Zuccaro MV, Xu J, Mitchell C, Marin D, Zimmerman R, Rana B, Weinstein E, King RT, Palmerola KL, Smith ME, Tsang SH, Goland R, Jasin M, Lobo R, Treff N, Egli D.
Zuccaro MV, et al. Among authors: rana b.
Cell. 2020 Dec 10;183(6):1650-1664.e15. doi: 10.1016/j.cell.2020.10.025. Epub 2020 Oct 29.
Cell. 2020.
PMID: 33125898
Free article.
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A novel test for annexin A5 M2 haplotyping in in vitro fertilization patients and preimplantation embryos.
Rana B, Zimmerman R, Marin D, Xu J, Messick E, Fishel S, Treff N.
Rana B, et al.
F S Sci. 2021 Aug;2(3):278-286. doi: 10.1016/j.xfss.2021.06.001. Epub 2021 Jun 9.
F S Sci. 2021.
PMID: 35560278
Free article.
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Utility and First Clinical Application of Screening Embryos for Polygenic Disease Risk Reduction.
Treff NR, Eccles J, Lello L, Bechor E, Hsu J, Plunkett K, Zimmerman R, Rana B, Samoilenko A, Hsu S, Tellier LCAM.
Treff NR, et al. Among authors: rana b.
Front Endocrinol (Lausanne). 2019 Dec 4;10:845. doi: 10.3389/fendo.2019.00845. eCollection 2019.
Front Endocrinol (Lausanne). 2019.
PMID: 31920964
Free PMC article.
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Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform.
Treff NR, Zimmerman R, Bechor E, Hsu J, Rana B, Jensen J, Li J, Samoilenko A, Mowrey W, Van Alstine J, Leondires M, Miller K, Paganetti E, Lello L, Avery S, Hsu S, Melchior Tellier LCA.
Treff NR, et al. Among authors: rana b.
Eur J Med Genet. 2019 Aug;62(8):103647. doi: 10.1016/j.ejmg.2019.04.004. Epub 2019 Apr 23.
Eur J Med Genet. 2019.
PMID: 31026593
Free article.
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