Szankasi P - Search Results

1

Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and Interpretation.

Shen W, Szankasi P, Durtschi J, Kelley TW, Xu X. Shen W, et al. Among authors: szankasi p. Methods Mol Biol. 2019;1908:113-124. doi: 10.1007/978-1-4939-9004-7_8. Methods Mol Biol. 2019. PMID: 30649724

2

Concurrent detection of targeted copy number variants and mutations using a myeloid malignancy next generation sequencing panel allows comprehensive genetic analysis using a single testing strategy.

Shen W, Szankasi P, Sederberg M, Schumacher J, Frizzell KA, Gee EP, Patel JL, South ST, Xu X, Kelley TW. Shen W, et al. Among authors: szankasi p. Br J Haematol. 2016 Apr;173(1):49-58. doi: 10.1111/bjh.13921. Epub 2016 Jan 5. Br J Haematol. 2016. PMID: 26728869 Free article. Clinical Trial.

3

Detection and Quantification of Acute Myeloid Leukemia-Associated Fusion Transcripts.

Schumacher J, Szankasi P, Kelley TW. Schumacher J, et al. Among authors: szankasi p. Methods Mol Biol. 2017;1633:151-161. doi: 10.1007/978-1-4939-7142-8_10. Methods Mol Biol. 2017. PMID: 28735486

4

Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.

Shen W, Paxton CN, Szankasi P, Longhurst M, Schumacher JA, Frizzell KA, Sorrells SM, Clayton AL, Jattani RP, Patel JL, Toydemir R, Kelley TW, Xu X. Shen W, et al. Among authors: szankasi p. J Clin Pathol. 2018 Apr;71(4):372-378. doi: 10.1136/jclinpath-2017-204823. Epub 2017 Dec 2. J Clin Pathol. 2018. PMID: 29197855

5

A comparison of deep sequencing of TCRG rearrangements vs traditional capillary electrophoresis for assessment of clonality in T-Cell lymphoproliferative disorders.

Schumacher JA, Duncavage EJ, Mosbruger TL, Szankasi PM, Kelley TW. Schumacher JA, et al. Am J Clin Pathol. 2014 Mar;141(3):348-59. doi: 10.1309/AJCP5TYGBVW4ZITR. Am J Clin Pathol. 2014. PMID: 24515762

6

Detection of FLT3 internal tandem duplication in targeted, short-read-length, next-generation sequencing data.

Spencer DH, Abel HJ, Lockwood CM, Payton JE, Szankasi P, Kelley TW, Kulkarni S, Pfeifer JD, Duncavage EJ. Spencer DH, et al. Among authors: szankasi p. J Mol Diagn. 2013 Jan;15(1):81-93. doi: 10.1016/j.jmoldx.2012.08.001. Epub 2012 Nov 14. J Mol Diagn. 2013. PMID: 23159595 Free article.

7

Molecular genetic biomarkers in myeloid malignancies.

Matynia AP, Szankasi P, Shen W, Kelley TW. Matynia AP, et al. Among authors: szankasi p. Arch Pathol Lab Med. 2015 May;139(5):594-601. doi: 10.5858/arpa.2014-0096-RA. Epub 2014 Aug 25. Arch Pathol Lab Med. 2015. PMID: 25152312 Free article. Review.

8

A novel approach to quantitating leukemia fusion transcripts by qRT-PCR without the need for standard curves.

Schumacher JA, Scott Reading N, Szankasi P, Matynia AP, Kelley TW. Schumacher JA, et al. Among authors: szankasi p. Exp Mol Pathol. 2015 Aug;99(1):104-8. doi: 10.1016/j.yexmp.2015.06.006. Epub 2015 Jun 14. Exp Mol Pathol. 2015. PMID: 26079545

9

Detection of BCR-ABL1 mutations that confer tyrosine kinase inhibitor resistance using massively parallel, next generation sequencing.

Szankasi P, Schumacher JA, Kelley TW. Szankasi P, et al. Ann Hematol. 2016 Jan;95(2):201-10. doi: 10.1007/s00277-015-2539-0. Epub 2015 Nov 10. Ann Hematol. 2016. PMID: 26555285

10

Molecular Fingerprinting of Anatomically and Temporally Distinct B-Cell Lymphoma Samples by Next-Generation Sequencing to Establish Clonal Relatedness.

Matynia AP, Li KD, Szankasi P, Schumacher J, Liew M, Salama ME, Kelley TW. Matynia AP, et al. Among authors: szankasi p. Arch Pathol Lab Med. 2019 Jan;143(1):105-111. doi: 10.5858/arpa.2017-0497-OA. Epub 2018 Jul 6. Arch Pathol Lab Med. 2019. PMID: 29979613 Free article.

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