IGH translocations in chronic lymphocytic leukemia: Clinicopathologic features and clinical outcomes von Fang, Hong, Reichard, Kaaren K., Rabe, Kari G., Hanson, Curtis A., Call, Timothy G., Ding, Wei, Kenderian, Saad S., Muchtar, Eli, Schwager, Susan M., Leis, Jose F., Chanan‐Khan, Asher A., Slager, Susan L., Braggio, Esteban, Smoley, Stephanie A., Kay, Neil E., Shanafelt, Tait D., Van Dyke, Daniel L., Parikh, Sameer A.

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Prospective Evaluation of Clonal Evolution During Long-Term Follow-Up of Patients With Untreated Early-Stage Chronic Lymphocytic Leukemia von SHANAFELT, Tait D, WITZIG, Thomas E, GEYER, Susan, ZENT, Clive S, CALL, Tim G, JELINEK, Diane F, KAY, Neil E, DEWALD, Gordon W, FINK, Stephanie R, JENKINS, Robert B, PATERNOSTER, Sarah F, SMOLEY, Stephanie A, STOCKERO, Kimberly J, NAST, Danielle M, FLYNN, Heather C, TSCHUMPER, Renee C

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Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia von Pitel, Beth A., Zepeda-Mendoza, Cinthya, Sachs, Zohar, Tang, Hongwei, Shivaram, Suganti, Sharma, Neeraj, Smadbeck, James B., Smoley, Stephanie A., Pearce, Kathryn E., Luoma, Ivy M., Cook, Joselle, Litzow, Mark R., Hoppman, Nicole L., Viswanatha, David, Xu, Xinjie, Ketterling, Rhett P., Greipp, Patricia T., Peterson, Jess F., Baughn, Linda B.

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Prenatal characterization of a novel inverted SMAD2 duplication by mate pair sequencing in a fetus with dextrocardia von Zepeda‐Mendoza, Cinthya J., Essendrup, Anna, Smoley, Stephanie A., Johnson, Sarah H., Hoppman, Nicole L, Vasmatzis, George, Jackson, Daniel L., Kearney, Hutton M., Baughn, Linda B.

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Fluorescence In Situ Hybridization to Visualize Genetic Abnormalities in Interphase Cells of Acinar Cell Carcinoma, Ductal Adenocarcinoma, and Islet Cell Carcinoma of the Pancreas von Dewald, Gordon W., PhD, Smyrk, Thomas C., MD, Thorland, Erik C., PhD, McWilliams, Robert R., MD, Van Dyke, Daniel L., PhD, Keefe, Jeannette G., BS, Belongie, Kimberly J., BS, Smoley, Stephanie A., BA, Knutson, Darlene L., BS, Fink, Stephanie R., BA, Wiktor, Anne E., BS, Petersen, Gloria M., PhD

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Metastatic clear cell papillary renal cell ‘tumour’ von Gupta, Sounak, Dasari, Surendra, Sharma, Vidit, Atwell, Thomas D, Sivasankaran, Gopinath, Smoley, Stephanie A, Hardcastle, Jayson J, Lohse, Christine M, Tekin, Burak, Jimenez, Rafael E, Thompson, R Houston, Boorjian, Stephen A, Leibovich, Bradley C, Cheville, John C

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Copy number variant analysis using genome‐wide mate‐pair sequencing von Smadbeck, James B., Johnson, Sarah H., Smoley, Stephanie A., Gaitatzes, Athanasios, Drucker, Travis M., Zenka, Roman M., Kosari, Farhad, Murphy, Stephen J., Hoppman, Nicole, Aypar, Umut, Sukov, William R., Jenkins, Robert B., Kearney, Hutton M., Feldman, Andrew L., Vasmatzis, George

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Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory von Peterson, Jess F., Sukov, William R., Pitel, Beth A., Smoley, Stephanie A., Pearce, Kathryn E., Meyer, Reid G., Williamson, Cynthia M., Smadbeck, James B., Vasmatzis, George, Hoppman, Nicole L., Greipp, Patricia T., Baughn, Linda B., Ketterling, Rhett P.

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SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq) von Johnson, Sarah H., Smadbeck, James B., Smoley, Stephanie A., Gaitatzes, Athanasios, Murphy, Stephen J., Harris, Faye R., Drucker, Travis M., Zenka, Roman M., Pitel, Beth A., Rowsey, Ross A., Hoppman, Nicole L., Aypar, Umut, Sukov, William R., Jenkins, Robert B., Feldman, Andrew L., Kearney, Hutton M., Vasmatzis, George

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Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia von Aypar, Umut, Smoley, Stephanie A., Pitel, Beth A., Pearce, Kathryn E., Zenka, Roman M., Vasmatzis, George, Johnson, Sarah H., Smadbeck, James B., Peterson, Jess F., Geiersbach, Katherine B., Van Dyke, Daniel L., Thorland, Erik C., Jenkins, Robert B., Ketterling, Rhett P., Greipp, Patricia T., Kearney, Hutton M., Hoppman, Nicole L., Baughn, Linda B.

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Clinical Validation of Tagmentation-Based Genome Sequencing for Germline Disorders von Shen, Wei, Sellers, Heidi L., Choate, Lauren A., Stein, Mariam I., Tandale, Pratyush P., Tan, Jiayu, Setlem, Rohit, Sakai, Yuta, Fadra, Numrah, Sosa, Carlos, McClelland, Shawn P., Barnett, Sarah S., Rasmussen, Kristen J., Runke, Cassandra K., Smoley, Stephanie A., Tillmans, Lori S., Marcou, Cherisse A., Rowsey, Ross A., Thorland, Erik C., Boczek, Nicole J., Kearney, Hutton M.

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Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemia von Peterson, Jess F., Pitel, Beth A., Smoley, Stephanie A., Smadbeck, James B., Johnson, Sarah H., Vasmatzis, George, Kearney, Hutton M., Greipp, Patricia T., Hoppman, Nicole L., Baughn, Linda B., Ketterling, Rhett P.

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The prognostic significance of del6q23 in chronic lymphocytic leukemia von Audil, Hadiyah Y., Hampel, Paul J., Van Dyke, Daniel L., Achenbach, Sara J., Rabe, Kari G., Smoley, Stephanie A., Call, Timothy G., Ding, Wei, Shi, Min, Hanson, Curtis A., Wang, Yucai, Muchtar, Eli, Koehler, Amber B., Schwager, Susan M., Leis, Jose F., Braggio, Esteban, Slager, Susan L., Kay, Neil E., Kenderian, Saad S., Parikh, Sameer A.

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A comprehensive evaluation of the prognostic significance of 13q deletions in patients with B‐chronic lymphocytic leukaemia von Van Dyke, Daniel L., Shanafelt, Tait D., Call, Timothy G., Zent, Clive S., Smoley, Stephanie A., Rabe, Kari G., Schwager, Susan M., Sonbert, Jessica C., Slager, Susan L., Kay, Neil E.

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Patients with chronic lymphocytic leukaemia and clonal deletion of both 17p13.1 and 11q22.3 have a very poor prognosis von Greipp, Patricia T., Smoley, Stephanie A., Viswanatha, David S., Frederick, Lori S., Rabe, Kari G., Sharma, Ruchi G., Slager, Susan L., Van Dyke, Daniel L., Shanafelt, Tait D., Tschumper, Renee C., Zent, Clive S.

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Mantle cell lymphoma with a novel t(11;12)(q13;p11.2): a proposed alternative mechanism of CCND1 up-regulation von Menke, Joshua R., Vasmatzis, George, Murphy, Stephen, Yang, Lin, Menke, David M., Tun, Han W., King, Rebecca L., Smoley, Stephanie A., Ketterling, Rhett P., Sukov, William R.

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Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TE... von Rowsey, Ross A., Smoley, Stephanie A., Williamson, Cynthia M., Vasmatzis, George, Smadbeck, James B., Ning, Yi, Greipp, Patricia T., Hoppman, Nicole L., Baughn, Linda B., Ketterling, Rhett P., Peterson, Jess F.

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Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation von Peterson, Jess F., Meyer, Reid G., Smoley, Stephanie A., Webley, Matthew, Smadbeck, James B., Vasmatzis, George, Pearce, Kathryn, Greipp, Patricia T., Ketterling, Rhett P., Craig, Fiona E., Stewart, A. Keith, Baughn, Linda B.

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Comparison of FISH, CpG-Stimulation, Chromosomal Microarray, and Mate-Pair Sequencing in 20 Patients With CLL or Lymphoma von Smoley, Stephanie A, Kearney, Hutton M, Van Dyke, Daniel L

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Elucidating a false-negative MYC break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with IGH/MYC... von Peterson, Jess F, Pitel, Beth A, Smoley, Stephanie A, Vasmatzis, George, Smadbeck, James B, Greipp, Patricia T, Ketterling, Rhett P, Macon, William R, Baughn, Linda B

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