Structures of BCL-2 in complex with venetoclax reveal the molecular basis of resistance mutations von Birkinshaw, Richard W., Gong, Jia-nan, Luo, Cindy S., Lio, Daisy, White, Christine A., Anderson, Mary Ann, Blombery, Piers, Lessene, Guillaume, Majewski, Ian J., Thijssen, Rachel, Roberts, Andrew W., Huang, David C. S., Colman, Peter M., Czabotar, Peter E.

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Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignancies von Sakuma, Maki, Blombery, Piers, Meggendorfer, Manja, Haferlach, Claudia, Lindauer, Markus, Martens, Uwe M., Kern, Wolfgang, Haferlach, Torsten, Walter, Wencke

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Bortezomib in the treatment of refractory thrombotic thrombocytopenic purpura von Patriquin, Christopher J., Thomas, Mari R., Dutt, Tina, McGuckin, Siobhan, Blombery, Piers A., Cranfield, Tanya, Westwood, John P., Scully, Marie

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Utility of Measurable Residual Disease (MRD) Assessment in Mantle Cell Lymphoma von Wu, Simon, Blombery, Piers, Westerman, David, Tam, Constantine S.

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Whole exome sequencing reveals activating JAK1 and STAT3 mutations in breast implant-associated anaplastic large cell lymphoma anaplastic large cell lymphoma von Blombery, Piers, Thompson, Ella R, Jones, Kate, Arnau, Gisela Mir, Lade, Stephen, Markham, John F, Li, Jason, Deva, Anand, Johnstone, Ricky W, Khot, Amit, Prince, H Miles, Westerman, David

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JAFFAL: detecting fusion genes with long-read transcriptome sequencing von Davidson, Nadia M, Chen, Ying, Sadras, Teresa, Ryland, Georgina L, Blombery, Piers, Ekert, Paul G, Göke, Jonathan, Oshlack, Alicia

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Clonal hematopoiesis, myeloid disorders and BAX-mutated myelopoiesis in patients receiving venetoclax for CLL von Blombery, Piers, Lew, Thomas E., Dengler, Michael A., Thompson, Ella R., Lin, Victor S., Chen, Xiangting, Nguyen, Tamia, Panigrahi, Ashish, Handunnetti, Sasanka M., Carney, Dennis A., Westerman, David A., Tam, Constantine S., Adams, Jerry M., Wei, Andrew H., Huang, David C.S., Seymour, John F., Roberts, Andrew W., Anderson, Mary Ann

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Variant acute promyelocytic leukaemia with novel NAB2::RARA fusion shows clinical all‐trans retinoic acid and arsenic trioxide sensitivity von Ng Liet Hing, Melissa, Ryland, Georgina L., Nguyen, Tamia, Tiong, Ing Soo, Dun, Karen, Ninkovic, Slavisa, Nedumannil, Rithin, Westerman, David A., Blombery, Piers A., Chan, Kah Lok, Bajel, Ashish

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Systemic diffuse large B-cell lymphoma involving the central nervous system have high rates of defective antigen presentation and immune surveillance von Wight, Joel, Blombery, Piers, Lickiss, Jennifer, Burgess, Melinda, Gould, Clare, Minson, Adrian, Swain, Fiona, Sabdia, Muhammed B., Gandhi, Maher K., Birchley, Andrew, Keane, Colm, Hawkes, Eliza A

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Clonal independence of JAK2 and CALR or MPL mutations in comutated myeloproliferative neoplasms demonstrated by single cell DNA sequencing von Thompson, Ella R., Nguyen, Tamia, Kankanige, Yamuna, Yeh, Paul, Ingbritsen, Michael, McBean, Michelle, Semple, Timothy, Arnau, Gisela Mir, Burbury, Kate, Lee, Nora, Khot, Amit, Westerman, David, Blombery, Piers

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Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphoma von Blombery, Piers, Thompson, Ella, Ryland, Georgina L, Joyce, Rachel, Byrne, David J, Khoo, Christine, Lade, Stephen, Hertzberg, Mark, Hapgood, Greg, Marlton, Paula, Deva, Anand, Lindeman, Geoffrey, Fox, Stephen, Westerman, David, Prince, Miles

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T cell receptor beta locus sequencing early post-allogeneic stem cell transplant identifies patients at risk of initial and recurrent cytomegalovirus infection von Kuzich, James A., Kankanige, Yamuna, Guinto, Jerick, Ryland, Georgina, McBean, Michelle, Wong, Eric, Koldej, Rachel, Collins, Jenny, Westerman, David, Ritchie, David, Blombery, Piers

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Molecular disease monitoring using circulating tumor DNA in myelodysplastic syndromes von Yeh, Paul, Dickinson, Michael, Ftouni, Sarah, Hunter, Tane, Sinha, Devbarna, Wong, Stephen Q., Agarwal, Rishu, Vedururu, Ravikiran, Doig, Kenneth, Fong, Chun Yew, Blombery, Piers, Westerman, David, Dawson, Mark A., Dawson, Sarah-Jane

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Circulating tumour DNA reflects treatment response and clonal evolution in chronic lymphocytic leukaemia von Yeh, Paul, Hunter, Tane, Sinha, Devbarna, Ftouni, Sarah, Wallach, Elise, Jiang, Damian, Chan, Yih-Chih, Wong, Stephen Q., Silva, Maria Joao, Vedururu, Ravikiran, Doig, Kenneth, Lam, Enid, Arnau, Gisela Mir, Semple, Timothy, Wall, Meaghan, Zivanovic, Andjelija, Agarwal, Rishu, Petrone, Pasquale, Jones, Kate, Westerman, David, Blombery, Piers, Seymour, John F., Papenfuss, Anthony T., Dawson, Mark A., Tam, Constantine S., Dawson, Sarah-Jane

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T-cell replete allogeneic stem cell transplant for mantle cell lymphoma achieves durable disease control, including against TP53-mutated disease von Lew, Thomas E., Cliff, Edward R. S., Dickinson, Michael, Tam, Constantine S., Seymour, John F., Blombery, Piers, Bajel, Ashish, Ritchie, David, Khot, Amit

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The molecular pathogenesis of B-cell non-Hodgkin lymphoma von Blombery, Piers A., Wall, Meaghan, Seymour, John F.

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Detection of BRAF mutations in patients with hairy cell leukemia and related lymphoproliferative disorders von BLOMBERY, Piers A, WONG, Stephen Q, HEWITT, Chelsee A, DOBROVIC, Alexander, MAXWELL, Ellen L, JUNEJA, Surender, GRIGORIADIS, George, WESTERMAN, David A

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Erratum to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes von Blombery, Piers, Fox, Lucy, Ryland, Georgina L, Thompson, Ella R, Lickiss, Jennifer, McBean, Michelle, Yerneni, Satwica, Trainer, Alison, Hughes, David, Greenway, Anthea, Mechinaud, Francoise, Wood, Erica M, Lieschke, Graham J, Szer, Jeff, Barbaro, Pasquale, Roy, John, Wight, Joel, Lynch, Elly, Martyn, Melissa, Gaff, Clara, Ritchie, David

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CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing von Markham, John F., Yerneni, Satwica, Ryland, Georgina L., Leong, Huei San, Fellowes, Andrew, Thompson, Ella R., De Silva, Wasanthi, Kumar, Amit, Lupat, Richard, Li, Jason, Ellul, Jason, Fox, Stephen, Dickinson, Michael, Papenfuss, Anthony T., Blombery, Piers

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Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes von Blombery, Piers, Fox, Lucy C., Ryland, Georgina L., Thompson, Ella R., Lickiss, Jennifer, McBean, Michelle, Yerneni, Satwica, Hughes, David, Greenway, Anthea, Mechinaud, Francoise, Wood, Erica M., Lieschke, Graham J., Szer, Jeff, Barbaro, Pasquale, Roy, John, Wight, Joel, Lynch, Elly, Martyn, Melissa, Gaff, Clara, Ritchie, David

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