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Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies.
Jiang L, Pallavajjala A, Huang J, Haley L, Morsberger L, Stinnett V, Hardy M, Park R, Ament C, Finch A, Shane A, Parish R, Nozari A, Long P, Adams E, Smith K, Parimi V, Dougaparsad S, Long L, Gocke CD, Zou YS. Jiang L, et al. Among authors: stinnett v. J Mol Diagn. 2021 Apr;23(4):467-483. doi: 10.1016/j.jmoldx.2021.01.011. Epub 2021 Feb 10. J Mol Diagn. 2021. PMID: 33577993 Free article.
An Integrated Approach Including CRISPR/Cas9-Mediated Nanopore Sequencing, Mate Pair Sequencing, and Cytogenomic Methods to Characterize Complex Structural Rearrangements in Acute Myeloid Leukemia.
Phan M, Gomes MA, Stinnett V, Morsberger L, Hoppman NL, Pearce KE, Smith K, Phan B, Jiang L, Zou YS. Phan M, et al. Among authors: stinnett v. Biomedicines. 2024 Mar 7;12(3):598. doi: 10.3390/biomedicines12030598. Biomedicines. 2024. PMID: 38540211 Free PMC article.
A comprehensive approach to evaluate genetic abnormalities in multiple myeloma using optical genome mapping.
Zou YS, Klausner M, Ghabrial J, Stinnett V, Long P, Morsberger L, Murry JB, Beierl K, Gocke CD, Xian RR, Toomer KH, Ye JC, Orlowski RZ, Huff CA, Ali SA, Imus PH, Gocke CB, Tang G. Zou YS, et al. Among authors: stinnett v. Blood Cancer J. 2024 May 3;14(1):78. doi: 10.1038/s41408-024-01059-x. Blood Cancer J. 2024. PMID: 38702349 Free PMC article. No abstract available.
16 results