Chromosomal Rearrangements of 6p25.3 Define a New Subtype of Lymphomatoid Papulosis von Karai, Laszlo J, Kadin, Marshall E, Hsi, Eric D, Sluzevich, Jason C, Ketterling, Rhett P, Knudson, Ryan A, Feldman, Andrew L

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Gastroblastoma harbors a recurrent somatic MALAT1–GLI1 fusion gene von Graham, Rondell P, Nair, Asha A, Davila, Jaime I, Jin, Long, Jen, Jin, Sukov, William R, Wu, Tsung-Teh, Appelman, Henry D, Torres-Mora, Jorge, Perry, Kyle D, Zhang, Lizhi, Kloft-Nelson, Sara M, Knudson, Ryan A, Greipp, Patricia T, Folpe, Andrew L

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Spliceosome mutations involving SRSF2, SF3B1, and U2AF35 in chronic myelomonocytic leukemia: Prevalence, clinical correlates, and prognostic relevance von Patnaik, Mrinal M., Lasho, Terra L., Finke, Christy M., Hanson, Curtis A., Hodnefield, Janice M., Knudson, Ryan A., Ketterling, Rhett P., Pardanani, Animesh, Tefferi, Ayalew

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Prognostic irrelevance of ring sideroblast percentage in World Health Organization–defined myelodysplastic syndromes without excess blasts von Patnaik, Mrinal M., Hanson, Curtis A., Sulai, Nanna H., Hodnefield, Janice M., Knudson, Ryan A., Ketterling, Rhett P., Lasho, Terra L., Tefferi, Ayalew

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Clinical correlates of JAK2V617F allele burden in essential thrombocythemia von Kittur, Jaya, Knudson, Ryan A., Lasho, Terra L., Finke, Christy M., Gangat, Naseema, Wolanskyj, Alexandra P., Li, Chin‐Yang, Wu, Wenting, Ketterling, Rhett P., Pardanani, Animesh, Tefferi, Ayalew

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Large Chromosomal Rearrangements Yield Biomarkers to Distinguish Low-Risk From Intermediate- and High-Risk Prostate Cancer von Vasmatzis, George, Kosari, Farhad, Murphy, Stephen J., Terra, Simone, Kovtun, Irina V., Harris, Faye R., Zarei, Shabnam, Smadbeck, James B., Johnson, Sarah H., Gaitatzes, Athanasios G., Therneau, Terry M., Rangel, Laureano J., Knudson, Ryan A., Greipp, Patricia, Sukov, William R., Knutson, Darlene L., Kloft-Nelson, Sara M., Karnes, R. Jeffrey, Cheville, John C.

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t(8;9)(p22;p24)/PCM1-JAK2 activates SOCS2 and SOCS3 via STAT5 von Ehrentraut, Stefan, Nagel, Stefan, Scherr, Michaela E, Schneider, Björn, Quentmeier, Hilmar, Geffers, Robert, Kaufmann, Maren, Meyer, Corinna, Prochorec-Sobieszek, Monika, Ketterling, Rhett P, Knudson, Ryan A, Feldman, Andrew L, Kadin, Marshall E, Drexler, Hans G, MacLeod, Roderick A F

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Translocation t(11;14) and survival of patients with light chain (AL) amyloidosis von Bryce, Alan H, Ketterling, Rhett P, Gertz, Morie A, Lacy, Martha, Knudson, Ryan A, Zeldenrust, Steven, Kumar, Shaji, Hayman, Suzanne, Buadi, Francis, Kyle, Robert A, Greipp, Philip R, Lust, John A, Russell, Stephen, Rajkumar, S. Vincent, Fonseca, Rafael, Dispenzieri, Angela

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ALK-negative anaplastic large cell lymphoma is a genetically heterogeneous disease with widely disparate clinical outcomes von Parrilla Castellar, Edgardo R., Jaffe, Elaine S., Said, Jonathan W., Swerdlow, Steven H., Ketterling, Rhett P., Knudson, Ryan A., Sidhu, Jagmohan S., Hsi, Eric D., Karikehalli, Shridevi, Jiang, Liuyan, Vasmatzis, George, Gibson, Sarah E., Ondrejka, Sarah, Nicolae, Alina, Grogg, Karen L., Allmer, Cristine, Ristow, Kay M., Wilson, Wyndham H., Macon, William R., Law, Mark E., Cerhan, James R., Habermann, Thomas M., Ansell, Stephen M., Dogan, Ahmet, Maurer, Matthew J., Feldman, Andrew L.

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Chromosome 8p11.2 translocations: Prevalence, FISH analysis for FGFR1 and MYST3, and clinicopathologic correlates in a consecutive cohort of 13 cases from a single institution von Patnaik, Mrinal M., Gangat, Naseema, Knudson, Ryan A., Keefe, Jeannette G., Hanson, Curtis A., Pardanani, Animesh, Ketterling, Rhett P., Tefferi, Ayalew

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SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value von Patnaik, Mrinal M., Lasho, Terra L., Hodnefield, Janice M., Knudson, Ryan A., Ketterling, Rhett P., Garcia-Manero, Guillermo, Steensma, David P., Pardanani, Animesh, Hanson, Curtis A., Tefferi, Ayalew

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Trisomies in multiple myeloma: impact on survival in patients with high-risk cytogenetics von Kumar, Shaji, Fonseca, Rafael, Ketterling, Rhett P., Dispenzieri, Angela, Lacy, Martha Q., Gertz, Morie A., Hayman, Suzanne R., Buadi, Francis K., Dingli, David, Knudson, Ryan A., Greenberg, Alexandra, Russell, Stephen J., Zeldenrust, Steven R., Lust, John A., Kyle, Robert A., Bergsagel, Leif, Rajkumar, S. Vincent

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Rearrangements and Amplification of IER3 (IEX-1) Represent a Novel and Recurrent Molecular Abnormality in Myelodysplastic Syndromes von STEENSMA, David P, NEIGER, Jessemy D, KETTERLING, Rhett P, PORCHER, Julie C, KEATS, J. Jonathan, BERGSAGEL, P. Leif, DENNIS, Thomas R, KNUDSON, Ryan A, JENKINS, Robert B, SANTANA-DAVILA, Rafael, KUMAR, Rajiv

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Integrated mate-pair and RNA sequencing identifies novel, targetable gene fusions in peripheral T-cell lymphoma von Boddicker, Rebecca L., Razidlo, Gina L., Dasari, Surendra, Zeng, Yu, Hu, Guangzhen, Knudson, Ryan A., Greipp, Patricia T., Davila, Jaime I., Johnson, Sarah H., Porcher, Julie C., Smadbeck, James B., Eckloff, Bruce W., Billadeau, Daniel D., Kurtin, Paul J., McNiven, Mark A., Link, Brian K., Ansell, Stephen M., Cerhan, James R., Asmann, Yan W., Vasmatzis, George, Feldman, Andrew L.

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Isolated del(5q) in myeloid malignancies: Clinicopathologic and molecular features in 143 consecutive patients von Patnaik, Mrinal M., Lasho, Terra L., Finke, Christy M., Knudson, Ryan A., Ketterling, Rhett P., Chen, Dong, Hoyer, James D., Hanson, Curtis A., Tefferi, Ayalew

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Chromosome 1 abnormalities in myeloid malignancies: a literature survey and karyotype-phenotype associations von Caramazza, Domenica, Hussein, Kebede, Siragusa, Sergio, Pardanani, Animesh, Knudson, Ryan A., Ketterling, Rhett P., Tefferi, Ayalew

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Clinicopathologic and Genetic Characterization of Follicular Lymphomas Presenting in the Ovary Reveals 2 Distinct Subgroups von ÖZSAN, Nazan, BEDKE, Brent J, LAW, Mark E, INWARDS, David J, KETTERLING, Rhett P, KNUDSON, Ryan A, KEENEY, Gary L, DOGAN, Ahmet, FELDMAN, Andrew L

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Ancillary immunohistochemical and molecular testing in the classification of cutaneous sweat gland/duct neoplasms: A validation study with emphasis on histomorphologic correlation... von Nguyen, Amanda J., Johnson, Emma, Camilleri, Michael, Wieland, Carilyn, Lehman, Julia S., Agrawal, Shruti, Comfere, Nneka, Fadra, Numrah, Knudson, Ryan A., Greipp, Patricia, Halling, Kevin, (Ray) Guo, Ruifeng

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Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas von Vasmatzis, George, Johnson, Sarah H., Knudson, Ryan A., Ketterling, Rhett P., Braggio, Esteban, Fonseca, Rafael, Viswanatha, David S., Law, Mark E., Kip, N. Sertac, Özsan, Nazan, Grebe, Stefan K., Frederick, Lori A., Eckloff, Bruce W., Thompson, E. Aubrey, Kadin, Marshall E., Milosevic, Dragana, Porcher, Julie C., Asmann, Yan W., Smith, David I., Kovtun, Irina V., Ansell, Stephen M., Dogan, Ahmet, Feldman, Andrew L.

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Chromosome 9p24 abnormalities: prevalence, description of novel JAK2 translocations, JAK2V617F mutation analysis and clinicopathologic correlates von Patnaik, Mrinal M., Knudson, Ryan A., Gangat, Naseema, Hanson, Curtis A., Pardanani, Animesh, Tefferi, Ayalew, Ketterling, Rhett P.

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