Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia von Thomson, Daniel W., Shahrin, Nur Hezrin, Wang, Paul P. S., Wadham, Carol, Shanmuganathan, Naranie, Scott, Hamish S., Dinger, Marcel E., Hughes, Timothy P., Schreiber, Andreas W., Branford, Susan

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The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution von Singhal, Deepak, Wee, Li Yan A., Kutyna, Monika M., Chhetri, Rakchha, Geoghegan, Joel, Schreiber, Andreas W., Feng, Jinghua, Wang, Paul P.-S., Babic, Milena, Parker, Wendy T., Hiwase, Smita, Edwards, Suzanne, Moore, Sarah, Branford, Susan, Kuzmanovic, Teodora, Singhal, Nimit, Gowda, Raghu, Brown, Anna L., Arts, Peer, To, Luen B., Bardy, Peter G., Lewis, Ian D., D’Andrea, Richard J., Maciejewski, Jaroslaw P., Scott, Hamish S., Hahn, Christopher N., Hiwase, Devendra K.

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Resensitising proteasome inhibitor-resistant myeloma with sphingosine kinase 2 inhibition von Bennett, Melissa K., Li, Manjun, Tea, Melinda N., Pitman, Melissa R., Toubia, John, Wang, Paul P.-S., Anderson, Dovile, Creek, Darren J., Orlowski, Robert Z., Gliddon, Briony L., Powell, Jason A., Wallington-Beddoe, Craig T., Pitson, Stuart M.

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BAM-matcher: a tool for rapid NGS sample matching von Wang, Paul P S, Parker, Wendy T, Branford, Susan, Schreiber, Andreas W

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Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer von Singhal, Deepak, Hahn, Christopher N., Feurstein, Simone, Wee, Li Yan A., Moma, Luke, Kutyna, Monika M., Chhetri, Rakchha, Eshraghi, Leila, Schreiber, Andreas W., Feng, Jinghua, Wang, Paul P-S., Babic, Milena, Parker, Wendy T., Gao, Song, Moore, Sarah, Das, Soma, Thomas, David, Pattnaik, Swetansu, Brown, Anna L., D’Andrea, Richard J., Poplawski, Nicola K., Thomas, Daniel, Scott, Hamish S., Godley, Lucy A., Hiwase, Devendra K.

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Childhood acute myeloid leukemia shows a high level of germline predisposition von Samaraweera, Saumya E., Wang, Paul P.S., Li, Ka Leung, Casolari, Debora A., Feng, Jinghua, Pinese, Mark, Maung, Kyaw Ze Ya, Leo, Paul, Cowley, Mark, Perkins, Kelly, Smith, Amanda M., Ellis, Jonathan, Wee, Amilia, Hiwase, Devendra K., Scott, Hamish S., Schreiber, Andreas W., Brown, Anna L., Deans, Andrew J., Ross, David M., Moore, Andrew S., Gonda, Thomas J., Hahn, Christopher N., D'Andrea, Richard J.

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The Genomic Landscape of Sporadic Prolactinomas von De Sousa, Sunita M. C., Wang, Paul P. S., Santoreneos, Stephen, Shen, Angeline, Yates, Christopher J., Babic, Milena, Eshraghi, Leila, Feng, Jinghua, Koszyca, Barbara, Roberts-Thomson, Samuel, Schreiber, Andreas W., Torpy, David J., Scott, Hamish S.

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ASXL1 and BIM germ line variants predict response and identify CML patients with the greatest risk of imatinib failure von Marum, Justine E., Yeung, David T., Purins, Leanne, Reynolds, John, Parker, Wendy T., Stangl, Doris, Wang, Paul P.S., Price, David J., Tuke, Jonathan, Schreiber, Andreas W., Scott, Hamish S., Hughes, Timothy P., Branford, Susan

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The scientification of China von Sun, Zhaohao, Wang, Paul P

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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML von Brown, Anna L., Arts, Peer, Carmichael, Catherine L., Babic, Milena, Dobbins, Julia, Chong, Chan-Eng, Schreiber, Andreas W., Feng, Jinghua, Phillips, Kerry, Wang, Paul P.S., Ha, Thuong, Homan, Claire C., King-Smith, Sarah L., Rawlings, Lesley, Vakulin, Cassandra, Dubowsky, Andrew, Burdett, Jessica, Moore, Sarah, McKavanagh, Grace, Henry, Denae, Wells, Amanda, Mercorella, Belinda, Nicola, Mario, Suttle, Jeffrey, Wilkins, Ella, Li, Xiao-Chun, Michaud, Joelle, Brautigan, Peter, Cannon, Ping, Altree, Meryl, Jaensch, Louise, Fine, Miriam, Butcher, Carolyn, D'Andrea, Richard J., Lewis, Ian D., Hiwase, Devendra K., Papaemmanuil, Elli, Horwitz, Marshall S., Natsoulis, Georges, Rienhoff, Hugh Y., Patton, Nigel, Mapp, Sally, Susman, Rachel, Morgan, Susan, Cooney, Julian, Currie, Mark, Popat, Uday, Bochtler, Tilmann, Izraeli, Shai, Bradstock, Kenneth, Godley, Lucy A., Krämer, Alwin, Fröhling, Stefan, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Poplawski, Nicola K., Hahn, Christopher N., Scott, Hamish S.

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Advances in Fuzzy Sets, Possibility Theory, and Applications von Wang, Paul P

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Germline Genetic Variation of ASXL1 and BIM Predicts Response to Imatinib and Identifies a Subset of High Sokal Risk Patients with the Greatest Risk of Treatment Failure and Diseas... von Marum, Justine E, Purins, Leanne, Yeung, David T, Parker, Wendy Tara, Price, David J, Wang, Paul PS, Stangl, Doris, Geogievski, Jasmina, Chereda, Bradley, Schreiber, Andreas, Tuke, Simon J, Hughes, Timothy P., Branford, Susan

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High Incidence of Mutated Cancer-Associated Genes at Diagnosis in CML Patients with Early Transformation to Blast Crisis von Branford, Susan, Wang, Paul PS, Parker, Wendy Tara, Yeung, David, Marum, Justine E, Stangl, Doris, Donaldson, Zoe, Yeoman, Alexandra, Nataren, Nathalie, Walker, Ieuan, Purins, Leanne, Chereda, Bradley, Hahn, Christopher N, Scott, Hamish S, Schreiber, Andreas, Hughes, Timothy P.

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Novel Fusion Genes at CML Diagnosis Reveal a Complex Pattern of Genomic Rearrangements and Sequence Inversions Associated with the Philadelphia Chromosome in Patients with Early Bl... von Marum, Justine E, Wang, Paul PS, Stangl, Doris, Yeung, David T., Mueller, Martin C., Dietz, Christian T., Walker, Ieuan, Nataren, Nathalie, Donaldson, Zoe, Parker, Wendy T, Ross, David M., Scott, Hamish S, Hughes, Timothy P., Schreiber, Andreas W, Branford, Susan

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Human embryonic stem cell (hESC) and human embryo research von Shand, Jessica, Berg, Jessica, Bogue, Clifford

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A note from Editor-in-Chief von Wang, P

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ADVANCES IN FUZZY SETS - AN OVERVIEW von Kaufmann, Arnold

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FUZZY PROGRAMMING: WHY AND HOW? - SOME HINTS AND EXAMPLES von Prade, Henri

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DECISION SUPPORT WITH FUZZY PRODUCTION SYSTEMS von Whalen, Thomas, Schott, Brian

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FUZZY SET STRUCTURE WITH STRONG IMPLICATION von Jinwen, Zhang

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