Showing 1 - 20 results of 36 for search 'Papaemmanuil, E', query time: 0.42s
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Perturbed hematopoietic stem and progenitor cell hierarchy in myelodysplastic syndromes patients with monosomy 7 as the sole cytogenetic abnormality. by Dimitriou, M, Woll, P, Mortera-Blanco, T, Karimi, M, Wedge, D, Doolittle, H, Douagi, I, Papaemmanuil, E, Jacobsen, S, Hellström-Lindberg, E
Published 2016Journal article -
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Genome-wide homozygosity signatures and childhood acute lymphoblastic leukemia risk. by Hosking, F, Papaemmanuil, E, Sheridan, E, Kinsey, SE, Lightfoot, T, Roman, E, Irving, J, Allan, J, Taylor, M, Tomlinson, I, Greaves, M, Houlston, R
Published 2010Journal article -
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Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. by Papaemmanuil, E, Hosking, F, Vijayakrishnan, J, Price, A, Olver, B, Sheridan, E, Kinsey, SE, Lightfoot, T, Roman, E, Irving, J, Allan, J, Tomlinson, I, Taylor, M, Greaves, M, Houlston, R
Published 2009Journal article -
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MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemia. by Hosking, F, Leslie, S, Dilthey, A, Moutsianas, L, Wang, Y, Dobbins, SE, Papaemmanuil, E, Sheridan, E, Kinsey, SE, Lightfoot, T, Roman, E, Irving, J, Allan, J, Taylor, M, Greaves, M, McVean, G, Houlston, R
Published 2011Journal article -
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COMPREHENSIVE ANALYSIS OF MUTATION STATUS, GENE EXPRESSION PROFILES, BLOOD AND BONE MARROW COUNTS AND OUTCOME IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES by Pellagatti, A, Gerstung, M, Papaemmanuil, E, Malcovati, L, Giagounidis, A, Della Porta, MG, Jadersten, M, Dolatshad, H, Verma, A, Cross, N, Vyas, P, Killick, S, Hellstrom-Lindberg, E, Cazzola, M, Campbell, P, Boultwood, J
Published 2014Conference item -
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Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations by Pellagatti, A, Steeples, V, Sharma, E, Repapi, E, Yip, B, Armstrong, R, Dolatshad, H, Lockstone, H, Taylor, S, Giagounidis, A, Vyas, P, Papaemmanuil, E, Woll, P, Killick, S, Malcovati, L, Hellstrom-Lindberg, E, Cazzola, M, Smith, C, Boultwood, J
Published 2017Conference item -
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Enasidenib induces acute myeloid leukemia cell differentiation to promote clinical response by Amatangelo, MD, Quek, L, Shih, A, Stein, EM, Roshal, M, David, MD, Marteyn, B, Farnoud, NR, De Botton, S, Bernard, OA, Wu, B, Yen, KE, Tallman, MS, Papaemmanuil, E, Penard-Lacronique, V, Thakurta, A, Vyas, P, Levine, RL
Published 2017Journal article -
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The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts. by Nikpour, M, Scharenberg, C, Liu, A, Conte, S, Karimi, M, Mortera-Blanco, T, Giai, V, Fernandez-Mercado, M, Papaemmanuil, E, Högstrand, K, Jansson, M, Vedin, I, Stephen Wainscoat, J, Campbell, P, Cazzola, M, Boultwood, J, Grandien, A, Hellström-Lindberg, E
Published 2013Journal article -
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High Throughput Targeted Gene Sequencing in 738 Myelodysplastic Syndromes Patients Reveals Novel Oncogenic Genes, Rare Driver Mutations and Complex Molecular Signatures with Potent... by Papaemmanuil, E, Gerstung, M, Malcovati, L, Tauro, S, Gundem, G, Van Loo, P, Pellagatti, A, Groves, M, Cross, N, Gambacorti-Passerini, C, Green, A, Boultwood, J, Vyas, P, Hellstrom-Lindberg, E, Bowen, D, Cazzola, M, Stratton, MR, Campbell, P
Published 2012Conference item -
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Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan (vol 15, pg 2903, 2006) by Kemp, Z, Carvajal-Carmona, L, Spain, S, Barclay, E, Gorman, M, Martin, L, Jaeger, E, Brooks, N, Bishop, D, Thomas, H, Tomlinson, I, Papaemmanuil, E, Webb, E, Sellick, G, Wood, W, Evans, G, Lucassen, A, Maher, E, Houlston, R, Identificat, C
Published 2006Journal article -
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Ezh2 and Runx1 mutations collaborate to initiate lympho-myeloid leukemia in early thymic progenitors by Booth, CAG, Barkas, N, Neo, WH, Boukarabila, H, Soilleux, EJ, Giotopoulos, G, Farnoud, N, Giustacchini, A, Ashley, N, Carrelha, J, Jamieson, L, Atkinson, D, Bouriez-Jones, T, Prinjha, RK, Milne, TA, Teachey, DT, Papaemmanuil, E, Huntly, BJP, Jacobsen, SEW, Mead, AJ
Published 2018Journal article -
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Modelling the progression of a preleukemic stage to overt leukemia in children with down syndrome by Labuhn, M, Perkins, K, Papaemmanuil, E, Garnett, C, Matzk, S, Amstislavskiy, V, Metzner, M, Kennedy, A, Scheer, C, Yoshida, K, Schwarzer, A, Crispino, J, Taub, J, Weiss, M, Ito, E, Ogawa, S, Reinhardt, D, Yaspo, M, Campbell, P, Heckl, D, Klusmann, J, Vyas, P
Published 2018Conference item -
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The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts by Nikpour, M, Scharenberg, C, Scharenberg, C, Liu, A, Conte, S, Karimi, M, Mortera-Blanco, T, Giai, V, Fernandez-Mercado, M, Papaemmanuil, E, Högstrand, K, Jansson, M, Vedin, I, Stephen Wainscoat, J, Campbell, P, Campbell, P, Cazzola, M, Cazzola, M, Boultwood, J, Grandien, A, Hellström-Lindberg, E
Published 2013Journal article -
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A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. by Broderick, P, Carvajal-Carmona, L, Pittman, A, Webb, E, Howarth, K, Rowan, A, Lubbe, S, Spain, S, Sullivan, K, Fielding, S, Jaeger, E, Vijayakrishnan, J, Kemp, Z, Gorman, M, Chandler, I, Papaemmanuil, E, Penegar, S, Wood, W, Sellick, G, Qureshi, M, Teixeira, A, Domingo, E, Barclay, E, Martin, L, Sieber, O
Published 2007Journal article -
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Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. by Jaeger, E, Webb, E, Howarth, K, Carvajal-Carmona, L, Rowan, A, Broderick, P, Walther, A, Spain, S, Pittman, A, Kemp, Z, Sullivan, K, Heinimann, K, Lubbe, S, Domingo, E, Barclay, E, Martin, L, Gorman, M, Chandler, I, Vijayakrishnan, J, Wood, W, Papaemmanuil, E, Penegar, S, Qureshi, M, Farrington, S, Tenesa, A
Published 2008Journal article -
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Deciphering the genetics of hereditary non-syndromic colorectal cancer. by Papaemmanuil, E, Carvajal-Carmona, L, Sellick, G, Kemp, Z, Webb, E, Spain, S, Sullivan, K, Barclay, E, Lubbe, S, Jaeger, E, Vijayakrishnan, J, Broderick, P, Gorman, M, Martin, L, Lucassen, A, Bishop, D, Evans, D, Maher, E, Steinke, V, Rahner, N, Schackert, H, Goecke, T, Holinski-Feder, E, Propping, P, Van Wezel, T
Published 2008Journal article -
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia by Piazza, R, Valletta, S, Winkelmann, N, Winkelmann, N, Redaelli, S, Spinelli, R, Pirola, A, Antolini, L, Mologni, L, Donadoni, C, Papaemmanuil, E, Schnittger, S, Kim, D, Boultwood, J, Rossi, F, Gaipa, G, De Martini, G, Di Celle, P, Jang, H, Jang, H, Fantin, V, Fantin, V, Bignell, G, Magistroni, V, Haferlach, T
Published 2013Journal article -
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Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms. by Malcovati, L, Papaemmanuil, E, Bowen, D, Boultwood, J, Della Porta, MG, Pascutto, C, Travaglino, E, Groves, M, Godfrey, A, Ambaglio, I, Gallì, A, Vià, D, Conte, S, Tauro, S, Keenan, N, Hyslop, A, Hinton, J, Mudie, L, Wainscoat, J, Futreal, P, Stratton, MR, Campbell, P, Hellström-Lindberg, E, Cazzola, M
Published 2011Journal article -
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. by Piazza, R, Valletta, S, Winkelmann, N, Redaelli, S, Spinelli, R, Pirola, A, Antolini, L, Mologni, L, Donadoni, C, Papaemmanuil, E, Schnittger, S, Kim, D, Boultwood, J, Rossi, F, Gaipa, G, De Martini, G, di Celle, P, Jang, H, Fantin, V, Bignell, G, Magistroni, V, Haferlach, T, Pogliani, E, Campbell, P, Chase, A
Published 2013Journal article