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Molecular genetic biomarkers in myeloid malignancies.
Matynia AP, Szankasi P, Shen W, Kelley TW. Matynia AP, et al. Among authors: shen w. 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.
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. 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.
Assessment of isochromosome 12p and 12p abnormalities in germ cell tumors using fluorescence in situ hybridization, single-nucleotide polymorphism arrays, and next-generation sequencing/mate-pair sequencing.
Freitag CE, Sukov WR, Bryce AH, Berg JV, Vanderbilt CM, Shen W, Smadbeck JB, Greipp PT, Ketterling RP, Jenkins RB, Herrera-Hernandez L, Costello BA, Thompson RH, Boorjian SA, Leibovich BC, Jimenez RE, Murphy SJ, Vasmatzis G, Cheville JC, Gupta S. Freitag CE, et al. Among authors: shen w. Hum Pathol. 2021 Jun;112:20-34. doi: 10.1016/j.humpath.2021.03.008. Epub 2021 Mar 31. Hum Pathol. 2021. PMID: 33798590
9,016 results