Galactomannan and PCR versus culture and histology for directing use of antifungal treatment for invasive aspergillosis in high-risk haematology patients: a randomised controlled t... von Morrissey, C Orla, Dr, Chen, Sharon C-A, MBBS, Sorrell, Tania C, Prof, Milliken, Samuel, MBBS, Bardy, Peter G, MBBS, Bradstock, Kenneth F, Prof, Szer, Jeffrey, Prof, Halliday, Catriona L, PhD, Gilroy, Nicole M, MBBS, Moore, John, MBBS, Schwarer, Anthony P, Prof, Guy, Stephen, MBBS, Bajel, Ashish, MBBS, Tramontana, Adrian R, MBBS, Spelman, Timothy, MBBS, Slavin, Monica A, Prof

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Polymorphism in Human Cytomegalovirus UL40 Impacts on Recognition of Human Leukocyte Antigen-E (HLA-E) by Natural Killer Cells von Heatley, Susan L., Pietra, Gabriella, Lin, Jie, Widjaja, Jacqueline M.L., Harpur, Christopher M., Lester, Sue, Rossjohn, Jamie, Szer, Jeff, Schwarer, Anthony, Bradstock, Kenneth, Bardy, Peter G., Mingari, Maria Cristina, Moretta, Lorenzo, Sullivan, Lucy C., Brooks, Andrew G.

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Red cell alloimmunization is associated with development of autoantibodies and increased red cell transfusion requirements in myelodysplastic syndrome von Singhal, Deepak, Kutyna, Monika M, Chhetri, Rakchha, Wee, Li Yan A, Hague, Sophia, Nath, Lakshmi, Nath, Shriram V, Sinha, Romi, Wickham, Nicholas, Lewis, Ian D, Ross, David M, Bardy, Peter G, To, Luen Bik, Reynolds, John, Wood, Erica M, Roxby, David J, Hiwase, Devendra K

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Human Gastrointestinal Neoplasia‐Associated Myofibroblasts Can Develop from Bone Marrow‐Derived Cells Following Allogeneic Stem Cell Transplantation von Worthley, Daniel L., Ruszkiewicz, Andrew, Davies, Ruth, Moore, Sarah, Nivison‐Smith, Ian, Bik To, L., Browett, Peter, Western, Robyn, Durrant, Simon, So, Jason, Young, Graeme P., Mullighan, Charles G., Bardy, Peter G., Michael, Michael Z.

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Donor Mannose-Binding Lectin Deficiency Increases the Likelihood of Clinically Significant Infection after Liver Transplantation von Worthley, Daniel L., Johnson, Douglas F., Eisen, Damon P., Dean, Melinda M., Heatley, Susan L., Tung, John-Paul, Scott, Justin, Padbury, Robert T. A., Harley, Hugh A., Bardy, Peter G., Angus, Peter W., Mullighan, Charles G.

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A No-Prophylaxis Platelet-Transfusion Strategy for Hematologic Cancers von Stanworth, Simon J, Estcourt, Lise J, Powter, Gillian, Kahan, Brennan C, Dyer, Claire, Choo, Louise, Bakrania, Lekha, Llewelyn, Charlotte, Littlewood, Timothy, Soutar, Richard, Norfolk, Derek, Copplestone, Adrian, Smith, Neil, Kerr, Paul, Jones, Gail, Raj, Kavita, Westerman, David A, Szer, Jeffrey, Jackson, Nicholas, Bardy, Peter G, Plews, Dianne, Lyons, Simon, Bielby, Linley, Wood, Erica M, Murphy, Michael F

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Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia von Scott, Hamish S, Hahn, Christopher N, Chong, Chan-Eng, Carmichael, Catherine L, Wilkins, Ella J, Brautigan, Peter J, Li, Xiao-Chun, Babic, Milena, Lin, Ming, Carmagnac, Amandine, Lee, Young K, Kok, Chung H, Gagliardi, Lucia, Friend, Kathryn L, Ekert, Paul G, Butcher, Carolyn M, Brown, Anna L, Lewis, Ian D, To, L Bik, Timms, Andrew E, Storek, Jan, Moore, Sarah, Altree, Meryl, Escher, Robert, Bardy, Peter G, Suthers, Graeme K, D'Andrea, Richard J, Horwitz, Marshall S

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Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature von Kazenwadel, Jan, Secker, Genevieve A., Liu, Yajuan J., Rosenfeld, Jill A., Wildin, Robert S., Cuellar-Rodriguez, Jennifer, Hsu, Amy P., Dyack, Sarah, Fernandez, Conrad V., Chong, Chan-Eng, Babic, Milena, Bardy, Peter G., Shimamura, Akiko, Zhang, Michael Y., Walsh, Tom, Holland, Steven M., Hickstein, Dennis D., Horwitz, Marshall S., Hahn, Christopher N., Scott, Hamish S., Harvey, Natasha L.

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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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Mannose-binding lectin and maladies of the bowel and liver von Worthley, Daniel-L, Bardy, Peter-G, Gordon, David-L, Mullighan, Charles-G

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Investigation of the expression of the EphB4 receptor tyrosine kinase in prostate carcinoma von Lee, Yen-Ching, Perren, Janeanne R, Douglas, Evelyn L, Raynor, Michael P, Bartley, Maria A, Bardy, Peter G, Stephenson, Sally-Anne

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Novel modes of MPL activation in triple-negative myeloproliferative neoplasms von Samaraweera, Saumya E., Geukens, Tatjana, Casolari, Debora A., Nguyen, Tran, Sun, Caitlyn, Bailey, Sheree, Moore, Sarah, Feng, Jinghua, Schreiber, Andreas W., Parker, Wendy T., Brown, Anna L., Butcher, Carolyn, Bardy, Peter G., Osborn, Michael, Scott, Hamish S., Talaulikar, Dipti, Grove, Carolyn S., Hahn, Christopher N., D'Andrea, Richard J., Ross, David M.

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Peripheral Blood Haploidentical Allogeneic Stem Cell Transplantation in Older Adults with Acute Myeloid Leukemia and Myelodysplastic Syndromes Demonstrates Long Term Survival, Resu... von Abadir, Edward, Othman, Jad, Kwan, John, Gottlieb, David J., Kennedy, Glen A., Bajel, Ashish, Doocey, Richard, Perera, Travis, Watson, Anne-Marie, Bardy, Peter G., Greenwood, Matthew, Curtis, David J., Tran, Steven, Moore, John, Hamad, Nada

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Mannose-binding Lectin and Infection Following Allogeneic Hemopoietic Stem Cell Transplantation von MULLIGHAN, CHARLES G, BARDY, PETER G

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Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion von Venugopal, Parvathy, Arts, Peer, Fox, Lucy C., Simons, Annet, Hiwase, Devendra K., Bardy, Peter G., Swift, Annette, Ross, David M., van Vulpen, Lize F. D., Buijs, Arjan, Bolton, Kelly L., Getta, Bartlomiej, Furlong, Eliska, Carter, Tina, Krapels, Ingrid, Hoeks, Marlijn, Al Kindy, Adila, Al Kindy, Farah, de Munnik, Sonja, Evans, Pamela, Frank, Mahalia S. B., Bournazos, Adam M., Cooper, Sandra T., Ha, Thuong Thi, Jackson, Matilda R., Arriola-Martinez, Luis, Phillips, Kerry, Brennan, Yvonne, Bakshi, Madhura, Ambler, Karen, Gao, Song, Kassahn, Karin S., Kenyon, Rosalie, Hung, Kevin, Babic, Milena, McGovern, Alan, Rawlings, Lesley, Vakulin, Cassandra, Dejong, Lucas, Fathi, Rema, McRae, Simon, Myles, Nicholas, Ladon, Dariusz, Jongmans, Marjolijn, Kuiper, Roland P., Poplawski, Nicola K., Barbaro, Pasquale, Blombery, Piers, Brown, Anna L., Hahn, Christopher N., Scott, Hamish S.

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Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation von Mullighan, Charles G., Heatley, Sue, Doherty, Kathleen, Szabo, Ferenc, Grigg, Andrew, Hughes, Timothy P., Schwarer, Anthony P., Szer, Jeff, Tait, Brian D., Bik To, L., Bardy, Peter G.

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Mannose-binding lectin status is associated with risk of major infection following myeloablative sibling allogeneic hematopoietic stem cell transplantation von Mullighan, Charles G., Heatley, Susan L., Danner, Silke, Dean, Melinda M., Doherty, Kathleen, Hahn, Uwe, Bradstock, Kenneth F., Minchinton, Robyn, Schwarer, Anthony P., Szer, Jeff, Bardy, Peter G.

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Clonal and lineage analysis of somatic DNMT3A and JAK2 mutations in a chronic phase polycythemia vera patient von Rao, Nisha, Butcher, Carolyn M., Lewis, Ian D., Ross, David M., Melo, Junia V., Scott, Hamish S., Bardy, Peter G., D'Andrea, Richard J.

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Tissue plasminogen activator -7351C/T enhancer polymorphism is a risk factor for lacunar stroke von JANNES, Jim, HAMILTON-BRUCE, Monica A, PILOTTO, Louis, SMITH, Brian J, MULLIGHAN, Charles G, BARDY, Peter G, KOBLAR, Simon A

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RUNX1 mutations are rare in chronic phase polycythaemia vera von Butcher, Carolyn M., Neufing, Petra J., Eriksson, Lena, Carmichael, Catherine L., Wilkins, Ella J., Melo, Junia V., Lewis, Ian D., Bardy, Peter G., Scott, Hamish S., D’Andrea, Richard J.

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