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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Power and powerlessness in a pandemic von Fine-Goulden, Miriam R.

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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia von Cheah, Jesse J C, Brown, Anna L, Schreiber, Andreas W, Feng, Jinghua, Babic, Milena, Moore, Sarah, Young, Chun-Chun, Fine, Miriam, Phillips, Kerry, Guandalini, Michael, Wilson, Peter, Poplawski, Nicola, Hahn, Christopher N, Scott, Hamish S

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Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient von Venugopal, Parvathy, Moore, Sarah, Lawrence, David M, George, Amee J, Hannan, Ross D, Bray, Sarah Ce, To, Luen Bik, D'Andrea, Richard J, Feng, Jinghua, Tirimacco, Amanda, Yeoman, Alexandra L, Young, Chun Chun, Fine, Miriam, Schreiber, Andreas W, Hahn, Christopher N, Barnett, Christopher, Saxon, Ben, Scott, Hamish S

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Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice von Meiser, Bettina, Kaur, Rajneesh, Morrow, April, Peate, Michelle, Wong, W K Tim, McPike, Emily, Cops, Elisa, Nichols, Cassandra, Austin, Rachel, Fine, Miriam, Thrupp, Letitia, Ward, Robyn, Macrae, Finlay, Hiller, Janet E, Trainer, Alison H, Mitchell, Gillian

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Mechanisms of ventilator dependence in children with neuromuscular and respiratory control disorders identified by monitoring diaphragm electrical activity von Fine-Goulden, Miriam R., Puppala, Naga K., Durward, Andrew

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How to use lactate von Fine-Goulden, Miriam R, Durward, Andrew

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Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies von Lewinsohn, Maya, Brown, Anna L., Weinel, Luke M., Phung, Connie, Rafidi, George, Lee, Ming K., Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Chong, Chan-Eng, Lee, Young, Yong, Agnes, Suthers, Graeme K., Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, D'Andrea, Richard J., Lewis, Ian D., Medeiros, Bruno C., Pollyea, Daniel A., King, Mary-Claire, Walsh, Tom, Keel, Siobán, Shimamura, Akiko, Godley, Lucy A., Hahn, Christopher N., Churpek, Jane E., Scott, Hamish S.

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Involving paediatricians-in-training in quality and service improvement von Fine-Goulden, Miriam R, Hanna, Sara

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An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families von Venugopal, Parvathy, Cheah, Jesse JC, Eshraghi, Leila, Shahrin, Nur Hezrin, Homan, Claire, Feng, Jinghua, Schreiber, Andreas W, Fine, Miriam, Phillips, Kerry, Poplawski, Nicola, Brown, Anna L, Hahn, Christopher N, Scott, Hamish S

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AN INTEGRATIVE GENOMIC APPROACH TO EXAMINE MUTATIONS AND BIOLOGICAL PATHWAYS ASSOCIATED WITH HAEMATOLOGICAL MALIGNANCY DEVELOPMENT IN DDX41 MUTATED FAMILIES von Cheah, Jesse, Brown, Anna, Eshraghi, Leila, Feng, Jinghua, Schreiber, Andreas, Babic, Milena, Homan, Claire, Fine, Miriam, Philips, Kerry, Poplawski, Nicola, Hahn, Christopher, Scott, Hamish

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Cor pulmonale due to congenital central hypoventilation syndrome presenting in adolescence von Fine-Goulden, Miriam R, Manna, Soumendu, Durward, Andrew

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IMPLICATIONS OF REVERTANT SOMATIC MOSAICISM IN BONE MARROW FAILURE SYNDROMES von Venugopal, Parvathy, Babic, Milena, Barnett, Christopher, Bray, Sarah, Brown, Anna, Cheah, Jesse, D'Andrea, Richard, Feng, Jinghua, Fine, Miriam, George, Amee, Guandalini, Michael, Hahn, Christopher, Hannan, Ross, Lawrence, David, Moore, Sarah, Philips, Kerry, Poplawski, Nicola, Saxon, Ben, Schreiber, Andreas, Scott, Hamish, Tirimacco, Amanda, To, Luen, Wilson, Peter, Yeoman, Alexandra, Young, Chun Chun

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A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship von Austin, Rachel, Brown, Jaye S., Madelli, Evanthia O., Das, Debjani, Soka, Magdalena, Blue, Gillian M., Atherton, John J., Quinn, Michael C.J., Poplawski, Nicola K., Weintraub, Robert G., De Fazio, Paul, Thompson, Tina, Macciocca, Ivan, Ingles, Jodie, McGaughran, Julie, McLean, Alison, Smyth, Renee, Fatkin, Diane, McNamara, James, Medi, Caroline, Al-Shinnag, Mohammad, Metke, Alejandro, Sy, Raymond, Atherton, John J., Finlay, Keri, Milnes, Di, Austin, Rachel, Milward, Michael, Bagnall, Richard D., Giannoulatou, Eleni, Morrish, Ansley, Taylor, Shelby, Barnett, Chris, Blue, Gillian M., Mountain, Helen, Thompson, Tina, Bodek, Simon, Boggs, Kirsten, Ng, Chai-Ann, Trainer, Alison, Bogwitz, Michael, Haas, Mathilda, Trivedi, Gunjan, Boughtwood, Tiffany, Martinez, Noelia Nunez, Hayward, Janette, Vandenberg, Jamie, Brown, Jaye, Herrera, Carmen, Verma, Kunal, Richardson, Rob Bryson, Hill, Adam, Pachter, Nicholas, Vidgen, Miranda, Patel, Chirag, Vohra, Jitendra, Burns, Charlotte, Perrin, Mark, Cao, Michelle, Horton, Ari E., Perry, Matthew, Howting, Denise, Pflaumer, Andreas, Weintraub, Robert G., Ingles, Jodie, Phillips, Peta, Wilson, Meredith, Chalinor, Heather, Phuong, Thuan, Winlaw, David, Chang, Yuchen, Jackson, Matilda, Worgan, Lisa, Charitou, Theosodia, Jane-Pantaleo, Sarah, Chong, Belinda, Johnson, Renee, Quinn, Michael C.J., Collins, Felicity, Quinn, Michael, Rajagopalan, Sulekha, Cox, Kathy, Kummerfeld, Sarah, Das, Debjani, Davis, Jason, Rogers, Jonathan, Lunke, Sebastian, Sandaradura, Sarah, Dobbins, Julia, Mansour, Julia, Sherburn, Isabella, Dunwoodie, Sally L., Dwyer, Nathan, Mathew, Jacob, Singer, Emma, Elbracht-Leong, Stefanie, Mattiske, Tessa, Smerdon, Carla, Elliott, David, McGaughran, Julie

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Decision making in long-term ventilation for children von Fine-Goulden, Miriam Rachel, Ray, Samiran, Brierley, Joe

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Expanded Phenotypic and Genetic Heterogeneity in the Clinical Spectrum of FPD-AML: Lymphoid Malignancies and Skin Disorders Are Common Features in Carriers of Germline RUNX1 Mutati... von Brown, Anna L, Hahn, Christopher N, Carmichael, Catherine, Wilkins, Ella, Babic, Milena, Chong, Chan-Eng, Li, Xiao-Chun, Michaud, Joelle, Cannon, Ping, Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, Schreiber, Andreas W, Feng, Jinghua, Rawlings, Lesley, Vakulin, Cassandra, Butcher, Carolyn, D'Andrea, Richard, Lewis, Ian D, Patton, Nigel, Forsyth, Cecily, Mapp, Sally, Mar Fan, Helen, Susman, Rachel, Morgan, Sue, Cooney, Julian, Currie, Mark S, Popat, Uday R., Bradstock, Kenneth, Sorrell, April D., Owen, Carolyn J., Horwitz, Marshall S, Hiwase, Devendra, Krämer, Alwin, Fröhling, Stefan, Godley, Lucy A, Churpek, Jane E, Scott, Hamish S

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Familial clustering of haematological malignancies: harbingers of wider germline cancer susceptibility von Scott, Hamish S., Brown, Anna L., Hiwase, Devendra, Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Poplawski, Nicola, Fine, Miriam, Rawlings, Lesley, Branford, Susan, Fuller, Stephen, Lewis, Ian, D’Andrea, Richard J., Hahn, Christopher N.

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Gaining clinical leadership experience through NHS England advisory support roles von Fine-Goulden, Miriam, Fielden, Jonathan

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Detection of t(2;5) in anaplastic large cell lymphoma : Comparison of immunohistochemical studies, FISH, and RT-PCR in paraffin-embedded tissue von CATALDO, K. A, JALAL, S. M, LAW, M. E, ANSELL, S. M, INWARDS, D. J, FINE, M, ARBER, D. A, PULFORD, K. A, STRICKLER, J. G

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Should Childhood Vaccination be Compulsory in the UK? von Fine-Goulden, Miriam

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