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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.
Lineage-Specific Alterations in Gynecologic Neoplasms with Choriocarcinomatous Differentiation: Implications for Origin and Therapeutics.
Xing D, Zheng G, Pallavajjala A, Schoolmeester JK, Liu Y, Haley L, Hu Y, Liu L, Logan L, Lin Y, Pearce KE, Sattler CA, Tsai YC, Vang R, Hung CF, Wu TC, Ronnett BM. Xing D, et al. Among authors: pallavajjala a. Clin Cancer Res. 2019 Jul 15;25(14):4516-4529. doi: 10.1158/1078-0432.CCR-18-4278. Epub 2019 Apr 22. Clin Cancer Res. 2019. PMID: 31010836
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
31 results