ETO-2 Associates with SCL in Erythroid Cells and Megakaryocytes and Provides Repressor Functions in Erythropoiesis von Schuh, Anna H., Tipping, Alex J., Clark, Allison J., Hamlett, Isla, Guyot, Boris, Iborra, Francesco J., Rodriguez, Patrick, Strouboulis, John, Enver, Tariq, Vyas, Paresh, Porcher, Catherine

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Efficacy of venetoclax monotherapy in patients with relapsed chronic lymphocytic leukaemia in the post‐BCR inhibitor setting: a UK wide analysis von Eyre, Toby A., Kirkwood, Amy A., Gohill, Sat, Follows, George, Walewska, Renata, Walter, Harriet, Cross, Matthew, Forconi, Francesco, Shah, Nimish, Chasty, Richard, Hart, Alistair, Broom, Angus, Marr, Helen, Patten, Piers E. M., Dann, Andy, Arumainathan, Arvind, Munir, Tal, Shankara, Paneesha, Bloor, Adrian, Johnston, Rosalynd, Orchard, Kim, Schuh, Anna H., Fox, Christopher P.

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Richter transformation of chronic lymphocytic leukaemia: a British Society for Haematology Good Practice Paper von Eyre, Toby A., Riches, John C., Patten, Piers E. M., Walewska, Renata, Marr, Helen, Follows, George, Hillmen, Peter, Schuh, Anna H.

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Guideline for the treatment of chronic lymphocytic leukaemia von Walewska, Renata, Parry‐Jones, Nilima, Eyre, Toby A., Follows, George, Martinez‐Calle, Nicolas, McCarthy, Helen, Parry, Helen, Patten, Piers E. M., Riches, John C., Hillmen, Peter, Schuh, Anna H.

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Idelalisib‐rituximab induces durable remissions in TP53 disrupted B‐PLL but results in significant toxicity: updated results of the UK‐wide compassionate use programme von Eyre, Toby A., Fox, Christopher P., Boden, Ali, Bloor, Adrian, Dungawalla, Moez, Shankara, Paneesha, Went, Richard, Schuh, Anna H.

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Applications of Nanopore sequencing in precision cancer medicine von Dyshlovoy, Sergey A., Paigin, Stefanie, Afflerbach, Ann‐Kristin, Lobermeyer, Annabelle, Werner, Stefan, Schüller, Ulrich, Bokemeyer, Carsten, Schuh, Anna H., Bergmann, Lina, Amsberg, Gunhild, Joosse, Simon A.

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Diagnostic dilemmas of high-grade transformation (Richter's syndrome) of chronic lymphocytic leukaemia: results of the phase II National Cancer Research Institute CHOP-OR clinical... von Soilleux, Elizabeth J, Wotherspoon, Andrew, Eyre, Toby A, Clifford, Ruth, Cabes, Maite, Schuh, Anna H

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Guideline for the treatment of chronic lymphocytic leukaemia: A British Society for Haematology Guideline von Schuh, Anna H, Parry-Jones, Nilima, Appleby, Niamh, Bloor, Adrian, Dearden, Claire E, Fegan, Christopher, Follows, George, Fox, Christopher P, Iyengar, Sunil, Kennedy, Ben, McCarthy, Helen, Parry, Helen M, Patten, Piers, Pettitt, Andrew R, Ringshausen, Ingo, Walewska, Renata, Hillmen, Peter

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Idelalisib‐Rituximab induces clinical remissions in patients with TP53 disrupted B cell prolymphocytic leukaemia von Eyre, Toby A., Fox, Christopher P., Shankara, Paneesha, Went, Richard, Schuh, Anna H.

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Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL von Klintman, Jenny, Barmpouti, Katerina, Knight, Samantha J. L., Robbe, Pauline, Dreau, Hélène, Clifford, Ruth, Ridout, Kate, Burns, Adam, Timbs, Adele, Bruce, David, Antoniou, Pavlos, Sosinsky, Alona, Becq, Jennifer, Bentley, David, Hillmen, Peter, Taylor, Jenny C., Caulfield, Mark, Schuh, Anna H.

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Guideline for the treatment of chronic lymphocytic leukaemia von Schuh, Anna H., Parry‐Jones, Nilima, Appleby, Niamh, Bloor, Adrian, Dearden, Claire E., Fegan, Christopher, Follows, George, Fox, Christopher P., Iyengar, Sunil, Kennedy, Ben, McCarthy, Helen, Parry, Helen M., Patten, Piers, Pettitt, Andrew R., Ringshausen, Ingo, Walewska, Renata, Hillmen, Peter

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Cardiac iron overload in transfusion‐dependent patients with myelodysplastic syndromes von Roy, Noémi B. A., Myerson, Saul, Schuh, Anna H., Bignell, Patricia, Patel, Roger, Wainscoat, Jim S., McGowan, Simon, Marchi, Emanuele, Atoyebi, Wale, Littlewood, Tim, Chacko, Joseph, Vyas, Paresh, Killick, Sally B.

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Dual dependence on BCL2 and MCL1 in T-cell prolymphocytic leukemia von Smith, Victoria M., Lomas, Oliver, Constantine, Donna, Palmer, Lianne, Schuh, Anna H., Bruce, David, Gonchar, Oksana, Macip, Salvador, Jayne, Sandrine, Dyer, Martin J.S., Eyre, Toby A.

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The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position von KHALIL, Mohamed S, MOLYNEUX, Adele T, MAROUF, Samy, ELDAMANHORY, Ghazy A, SCHUH, Anna H, HENDERSON, Shirley J, OLD, John M

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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases von Pagnamenta, Alistair T, Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M, Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J, Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R, Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V, Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L, Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R, Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E, Guerrini, Renzo, Harris, Adrian L, Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J L, Kreins, Alexandra Y, Kvikstad, Erika M, Langman, Craig B, Lester, Tracy, Lines, Kate E, Lord, Simon R, Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J, Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H, Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y, Pentony, Melissa M, Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G, Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D, Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V, Twigg, Stephen R F, Uhlig, Holm H, van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H, Kini, Usha, Wilkie, Andrew O M, Popitsch, Niko, Taylor, Jenny C

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Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods von Shields, Adrian M, Pagnamenta, Alistair T, Pollard, Andrew J, Taylor, Jenny C, Allroggen, Holger, Patel, Smita Y

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Comparative analysis of targeted novel therapies in relapsed, refractory chronic lymphocytic leukemia von Eyre, Toby A., Lamanna, Nicole, Roeker, Lindsey E., Ujjani, Chaitra S., Hill, Brian T., Barr, Paul M., Lansigan, Erick, Cheson, Bruce D., Yazdy, Maryam, Allan, John N., Rhodes, Joanna, Schuster, Stephen J., Nabhan, Chadi, Skarbnik, Alan, Leslie, Lorie, Islam, Prioty, Whitaker, Katherine, Coombs, Catherine C., Tuncer, Hande H., Pagel, John M., Jacobs, Ryan, Winter, Allison M., Bailey, Neil, Sitlinger, Andrea, Schuh, Anna H., Follows, George, Fox, Christopher P., Brander, Danielle M., Shadman, Mazyar, Mato, Anthony R.

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The Oncoprotein SCL/Tal-1 Associates with the Co-Repressor ETO-2 in Multiprotein Complexes in Erythroid Cells and Megakaryocytes von Schuh, Anna H., Hamlett, Isla, Strouboulis, John, Grosveld, Frank, Vyas, Paresh, Porcher, Catherine

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Additional file 3 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases von Pagnamenta, Alistair T., Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M., Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J., Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R., Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V., Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L., Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R., Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E. Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E., Guerrini, Renzo, Harris, Adrian L., Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J. L., Kreins, Alexandra Y., Kvikstad, Erika M., Langman, Craig B., Lester, Tracy, Lines, Kate E., Lord, Simon R., Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J., Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H., Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y., Pentony, Melissa M., Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G., Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D., Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V., Twigg, Stephen R. F., Uhlig, Holm H., van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H., Kini, Usha, Wilkie, Andrew O. M., Popitsch, Niko, Taylor, Jenny C.

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Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia von Klintman, Jenny, Appleby, Niamh, Stamatopoulos, Basile, Ridout, Katie, Eyre, Toby A., Robbe, Pauline, Pascua, Laura Lopez, Knight, Samantha J.L., Dreau, Helene, Cabes, Maite, Popitsch, Niko, Ehinger, Mats, Martín-Subero, Jose I., Campo, Elías, Månsson, Robert, Rossi, Davide, Taylor, Jenny C., Vavoulis, Dimitrios V., Schuh, Anna

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