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Haplotype counting by next-generation sequencing for ultrasensitive human DNA detection.
Debeljak M, Freed DN, Welch JA, Haley L, Beierl K, Iglehart BS, Pallavajjala A, Gocke CD, Leffell MS, Lin MT, Pevsner J, Wheelan SJ, Eshleman JR. Debeljak M, et al. Among authors: pallavajjala a. J Mol Diagn. 2014 Sep;16(5):495-503. doi: 10.1016/j.jmoldx.2014.04.003. J Mol Diagn. 2014. PMID: 25132481 Free PMC article.
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: pallavajjala a. 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.
IDH1 and IDH2 Mutations in Colorectal Cancers.
Huang J, Tseng LH, Parini V, Lokhandwala PM, Pallavajjala A, Rodriguez E, Xian R, Chen L, Gocke CD, Eshleman JR, Lin MT. Huang J, et al. Among authors: pallavajjala a. Am J Clin Pathol. 2021 Oct 13;156(5):777-786. doi: 10.1093/ajcp/aqab023. Am J Clin Pathol. 2021. PMID: 33929516
Artificial Intelligence-Assisted Serial Analysis of Clinical Cancer Genomics Data Identifies Changing Treatment Recommendations and Therapeutic Targets.
Fischer CG, Pallavajjala A, Jiang L, Anagnostou V, Tao J, Adams E, Eshleman JR, Gocke CD, Lin MT, Platz EA, Xian RR. Fischer CG, et al. Among authors: pallavajjala a. Clin Cancer Res. 2022 Jun 1;28(11):2361-2372. doi: 10.1158/1078-0432.CCR-21-4061. Clin Cancer Res. 2022. PMID: 35312750 Free PMC article.
32 results