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Year | Number of Results |
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2021 | 2 |
2022 | 2 |
2023 | 1 |
2024 | 1 |
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Page 1
Complex/cryptic EWSR1::FLI1/ERG Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas.
Genes (Basel). 2023 May 24;14(6):1139. doi: 10.3390/genes14061139.
Genes (Basel). 2023.
PMID: 37372318
Free PMC article.
Utility of targeted next-generation sequencing assay to detect 1p/19q co-deletion in formalin-fixed paraffin-embedded glioma specimens.
Pallavajjala A, Haley L, Stinnett V, Adams E, Pallavajjala R, Huang J, Morsberger L, Hardy M, Long P, Gocke CD, Eshleman JR, Rodriguez FJ, Zou YS.
Pallavajjala A, et al. Among authors: long p.
Hum Pathol. 2022 Aug;126:63-76. doi: 10.1016/j.humpath.2022.05.001. Epub 2022 May 10.
Hum Pathol. 2022.
PMID: 35561840
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HER2 amplification by next-generation sequencing to identify HER2-positive invasive breast cancer with negative HER2 immunohistochemistry.
Morsberger L, Pallavajjala A, Long P, Hardy M, Park R, Parish R, Nozari A, Zou YS.
Morsberger L, et al. Among authors: long p.
Cancer Cell Int. 2022 Nov 15;22(1):350. doi: 10.1186/s12935-022-02761-1.
Cancer Cell Int. 2022.
PMID: 36376842
Free PMC article.
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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: long p.
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.
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Diagnostic Utility of Gene Fusion Panel to Detect Gene Fusions in Fresh and Formalin-Fixed, Paraffin-Embedded Cancer Specimens.
Haley L, Parimi V, Jiang L, Pallavajjala A, Hardy M, Yonescu R, Morsberger L, Stinnett V, Long P, Zou YS, Gocke CD.
Haley L, et al. Among authors: long p.
J Mol Diagn. 2021 Oct;23(10):1343-1358. doi: 10.1016/j.jmoldx.2021.07.015. Epub 2021 Aug 4.
J Mol Diagn. 2021.
PMID: 34358677
Free article.
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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: long p.
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.
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