-
1
-
-
84878341989
-
Acute lymphoblastic leukaemia
-
Inaba H, Greaves M, Mullighan CG. Acute lymphoblastic leukaemia. Lancet. 2013; 381(9881):1943-1955.
-
(2013)
Lancet
, vol.381
, Issue.9881
, pp. 1943-1955
-
-
Inaba, H.1
Greaves, M.2
Mullighan, C.G.3
-
2
-
-
0036344108
-
Cytogenetics and molecular genetics of acute lymphoblastic leukemia
-
discussion 200-202
-
Harrison CJ, Foroni L. Cytogenetics and molecular genetics of acute lymphoblastic leukemia. Rev Clin Exp Hematol. 2002;6(2): 91-113, discussion 200-202.
-
(2002)
Rev Clin Exp Hematol.
, vol.6
, Issue.2
, pp. 91-113
-
-
Harrison, C.J.1
Foroni, L.2
-
3
-
-
42649124306
-
Molecular pathogenesis of T-cell leukaemia and lymphoma
-
Aifantis I, Raetz E, Buonamici S. Molecular pathogenesis of T-cell leukaemia and lymphoma. Nat Rev Immunol. 2008;8(5):380-390.
-
(2008)
Nat Rev Immunol.
, vol.8
, Issue.5
, pp. 380-390
-
-
Aifantis, I.1
Raetz, E.2
Buonamici, S.3
-
4
-
-
24944506539
-
Clinical characteristics, biologic features and outcome for young adult patients with acute lymphoblastic leukaemia
-
Nachman J. Clinical characteristics, biologic features and outcome for young adult patients with acute lymphoblastic leukaemia. Br J Haematol. 2005;130(2):166-173.
-
(2005)
Br J Haematol.
, vol.130
, Issue.2
, pp. 166-173
-
-
Nachman, J.1
-
5
-
-
84867145464
-
Molecular genetics of B-precursor acute lymphoblastic leukemia
-
Mullighan CG. Molecular genetics of B-precursor acute lymphoblastic leukemia. J Clin Invest. 2012;122(10):3407-3415.
-
(2012)
J Clin Invest.
, vol.122
, Issue.10
, pp. 3407-3415
-
-
Mullighan, C.G.1
-
6
-
-
84861633881
-
The pediatric cancer genome project
-
Downing JR, Wilson RK, Zhang J, et al. The pediatric cancer genome project. Nat Genet. 2012;44(6):619-622.
-
(2012)
Nat Genet.
, vol.44
, Issue.6
, pp. 619-622
-
-
Downing, J.R.1
Wilson, R.K.2
Zhang, J.3
-
7
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha S, Radtke I, et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature. 2007; 446(7137):758-764.
-
(2007)
Nature
, vol.446
, Issue.7137
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
-
8
-
-
34249733805
-
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression
-
Kuiper RP, Schoenmakers EF, van Reijmersdal SV, Hehir-Kwa JY, van Kessel AG, van Leeuwen FN, Hoogerbrugge PM. High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression. Leukemia. 2007;21(6):1258-1266.
-
(2007)
Leukemia
, vol.21
, Issue.6
, pp. 1258-1266
-
-
Kuiper, R.P.1
Schoenmakers, E.F.2
Van Reijmersdal, S.V.3
Hehir-Kwa, J.Y.4
Van Kessel, A.G.5
Van Leeuwen, F.N.6
Hoogerbrugge, P.M.7
-
9
-
-
43049139905
-
BCRABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros
-
Mullighan CG, Miller CB, Radtke I, et al. BCRABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature. 2008; 453(7191):110-114.
-
(2008)
Nature
, vol.453
, Issue.7191
, pp. 110-114
-
-
Mullighan, C.G.1
Miller, C.B.2
Radtke, I.3
-
10
-
-
79952381408
-
CREBBP mutations in relapsed acute lymphoblastic leukaemia
-
Mullighan CG, Zhang J, Kasper LH, et al. CREBBP mutations in relapsed acute lymphoblastic leukaemia. Nature. 2011; 471(7337):235-239.
-
(2011)
Nature
, vol.471
, Issue.7337
, pp. 235-239
-
-
Mullighan, C.G.1
Zhang, J.2
Kasper, L.H.3
-
11
-
-
80052922387
-
Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: A report from the Children's Oncology Group
-
Zhang J, Mullighan CG, Harvey RC, et al. Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group. Blood. 2011;118(11):3080-3087.
-
(2011)
Blood
, vol.118
, Issue.11
, pp. 3080-3087
-
-
Zhang, J.1
Mullighan, C.G.2
Harvey, R.C.3
-
12
-
-
5044225888
-
Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia
-
Weng AP, Ferrando AA, Lee W, et al. Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia. Science. 2004; 306(5694):269-271.
-
(2004)
Science
, vol.306
, Issue.5694
, pp. 269-271
-
-
Weng, A.P.1
Ferrando, A.A.2
Lee, W.3
-
13
-
-
70149087158
-
High frequency of PTEN, PI3K, and AKT abnormalities in T-cell acute lymphoblastic leukemia
-
Gutierrez A, Sanda T, Grebliunaite R, et al. High frequency of PTEN, PI3K, and AKT abnormalities in T-cell acute lymphoblastic leukemia. Blood. 2009;114(3):647-650.
-
(2009)
Blood
, vol.114
, Issue.3
, pp. 647-650
-
-
Gutierrez, A.1
Sanda, T.2
Grebliunaite, R.3
-
14
-
-
70349232830
-
WT1 mutations in T-ALL
-
Tosello V, Mansour MR, Barnes K, et al. WT1 mutations in T-ALL. Blood. 2009;114(5): 1038-1045.
-
(2009)
Blood
, vol.114
, Issue.5
, pp. 1038-1045
-
-
Tosello, V.1
Mansour, M.R.2
Barnes, K.3
-
15
-
-
34547780475
-
FBW7 mutations in leukemic cells mediate NOTCH pathway activation and resistance to gamma-secretase inhibitors
-
O'Neil J, Grim J, Strack P, et al. FBW7 mutations in leukemic cells mediate NOTCH pathway activation and resistance to gamma-secretase inhibitors. J Exp Med. 2007;204(8):1813-1824.
-
(2007)
J Exp Med.
, vol.204
, Issue.8
, pp. 1813-1824
-
-
O'Neil, J.1
Grim, J.2
Strack, P.3
-
16
-
-
34548009617
-
The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children
-
Clappier E, Cuccuini W, Kalota A, et al. The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children. Blood. 2007;110(4):1251-1261.
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1251-1261
-
-
Clappier, E.1
Cuccuini, W.2
Kalota, A.3
-
17
-
-
77950299929
-
PHF6 mutations in T-cell acute lymphoblastic leukemia
-
Van Vlierberghe P, Palomero T, Khiabanian H, et al. PHF6 mutations in T-cell acute lymphoblastic leukemia. Nat Genet. 2010;42(4): 338-342.
-
(2010)
Nat Genet.
, vol.42
, Issue.4
, pp. 338-342
-
-
Van Vlierberghe, P.1
Palomero, T.2
Khiabanian, H.3
-
18
-
-
78651299314
-
PHF6 mutations in adult acute myeloid leukemia
-
Van Vlierberghe P, Patel J, Abdel-Wahab O, et al. PHF6 mutations in adult acute myeloid leukemia. Leukemia. 2011;25(1):130-134.
-
(2011)
Leukemia
, vol.25
, Issue.1
, pp. 130-134
-
-
Van Vlierberghe, P.1
Patel, J.2
Abdel-Wahab, O.3
-
19
-
-
58749095816
-
Early T-cell precursor leukaemia: A subtype of very high-risk acute lymphoblastic leukaemia
-
Coustan-Smith E, Mullighan CG, Onciu M, et al. Early T-cell precursor leukaemia: a subtype of very high-risk acute lymphoblastic leukaemia. Lancet Oncol. 2009;10(2):147-156.
-
(2009)
Lancet Oncol.
, vol.10
, Issue.2
, pp. 147-156
-
-
Coustan-Smith, E.1
Mullighan, C.G.2
Onciu, M.3
-
20
-
-
37549010335
-
Launching the T-cell-lineage developmental programme
-
Rothenberg EV, Moore JE, Yui MA. Launching the T-cell-lineage developmental programme. Nat Rev Immunol. 2008;8(1):9-21.
-
(2008)
Nat Rev Immunol.
, vol.8
, Issue.1
, pp. 9-21
-
-
Rothenberg, E.V.1
Moore, J.E.2
Yui, M.A.3
-
21
-
-
84862907593
-
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
-
Zhang J, Ding L, Holmfeldt L, et al. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature. 2012; 481(7380):157-163.
-
(2012)
Nature
, vol.481
, Issue.7380
, pp. 157-163
-
-
Zhang, J.1
Ding, L.2
Holmfeldt, L.3
-
22
-
-
84875135862
-
Criteria for inference of chromothripsis in cancer genomes
-
Korbel JO, Campbell PJ. Criteria for inference of chromothripsis in cancer genomes. Cell. 2013; 152(6):1226-1236.
-
(2013)
Cell
, vol.152
, Issue.6
, pp. 1226-1236
-
-
Korbel, J.O.1
Campbell, P.J.2
-
23
-
-
84862776920
-
Reverse engineering of TLX oncogenic transcriptional networks identifies RUNX1 as tumor suppressor in T-ALL
-
Della Gatta G, Palomero T, Perez-Garcia A, et al. Reverse engineering of TLX oncogenic transcriptional networks identifies RUNX1 as tumor suppressor in T-ALL. Nat Med. 2012; 18(3):436-440.
-
(2012)
Nat Med.
, vol.18
, Issue.3
, pp. 436-440
-
-
Della Gatta, G.1
Palomero, T.2
Perez-Garcia, A.3
-
25
-
-
42249091014
-
Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia
-
Flex E, Petrangeli V, Stella L, et al. Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia. J Exp Med. 2008; 205(4):751-758.
-
(2008)
J Exp Med.
, vol.205
, Issue.4
, pp. 751-758
-
-
Flex, E.1
Petrangeli, V.2
Stella, L.3
-
26
-
-
79956108320
-
Gain-offunction mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias
-
Shochat C, Tal N, Bandapalli OR, et al. Gain-offunction mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias. J Exp Med. 2011;208(5):901-908.
-
(2011)
J Exp Med.
, vol.208
, Issue.5
, pp. 901-908
-
-
Shochat, C.1
Tal, N.2
Bandapalli, O.R.3
-
27
-
-
80053385665
-
Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia
-
Zenatti PP, Ribeiro D, Li W, et al. Oncogenic IL7R gain-of-function mutations in childhood T-cell acute lymphoblastic leukemia. Nat Genet. 2011;43(10):932-939.
-
(2011)
Nat Genet.
, vol.43
, Issue.10
, pp. 932-939
-
-
Zenatti, P.P.1
Ribeiro, D.2
Li, W.3
-
28
-
-
84863966948
-
Clinical and molecular characterization of early T-cell precursor leukemia: A high-risk subgroup in adult T-ALL with a high frequency of FLT3 mutations
-
Neumann M, Heesch S, Gokbuget N, et al. Clinical and molecular characterization of early T-cell precursor leukemia: a high-risk subgroup in adult T-ALL with a high frequency of FLT3 mutations. Blood cancer journal. 2012;2(1):e55.
-
(2012)
Blood Cancer Journal
, vol.2
, Issue.1
, pp. e55
-
-
Neumann, M.1
Heesch, S.2
Gokbuget, N.3
-
29
-
-
84856747744
-
Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia
-
Ntziachristos P, Tsirigos A, Van Vlierberghe P, et al. Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia. Nat Med. 2012;18(2): 298-301.
-
(2012)
Nat Med.
, vol.18
, Issue.2
, pp. 298-301
-
-
Ntziachristos, P.1
Tsirigos, A.2
Van Vlierberghe, P.3
-
30
-
-
84881041250
-
Wholeexome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations
-
Neumann M, Heesch S, Schlee C, et al. Wholeexome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations. Blood. 2013; 121(23):4749-4752.
-
(2013)
Blood
, vol.121
, Issue.23
, pp. 4749-4752
-
-
Neumann, M.1
Heesch, S.2
Schlee, C.3
-
31
-
-
6944252248
-
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia
-
Graux C, Cools J, Melotte C, et al. Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia. Nat Genet. 2004; 36(10):1084-1089.
-
(2004)
Nat Genet.
, vol.36
, Issue.10
, pp. 1084-1089
-
-
Graux, C.1
Cools, J.2
Melotte, C.3
-
32
-
-
84873084751
-
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia
-
De Keersmaecker K, Atak ZK, Li N, et al. Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia. Nat Genet. 2013; 45(2):186-190.
-
(2013)
Nat Genet.
, vol.45
, Issue.2
, pp. 186-190
-
-
De Keersmaecker, K.1
Atak, Z.K.2
Li, N.3
-
33
-
-
58749109707
-
Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia
-
Mullighan CG, Su X, Zhang J, et al; Children's Oncology Group. Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia. N Engl J Med. 2009;360(5):470-480.
-
(2009)
N Engl J Med.
, vol.360
, Issue.5
, pp. 470-480
-
-
Mullighan, C.G.1
Su, X.2
Zhang, J.3
-
34
-
-
58749097408
-
A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: A genome-wide classification study
-
Den Boer ML, van Slegtenhorst M, De Menezes RX, et al. A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study. Lancet Oncol. 2009;10(2):125-134.
-
(2009)
Lancet Oncol.
, vol.10
, Issue.2
, pp. 125-134
-
-
Den Boer, M.L.1
Van Slegtenhorst, M.2
De Menezes, R.X.3
-
35
-
-
84872457525
-
Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: A report from the Children's Oncology Group TARGET Project
-
Loh ML, Zhang J, Harvey RC, et al. Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project. Blood. 2013;121(3):485-488.
-
(2013)
Blood
, vol.121
, Issue.3
, pp. 485-488
-
-
Loh, M.L.1
Zhang, J.2
Harvey, R.C.3
-
36
-
-
70350519430
-
Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia
-
Russell LJ, Capasso M, Vater I, et al. Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia. Blood. 2009;114(13): 2688-2698.
-
(2009)
Blood
, vol.114
, Issue.13
, pp. 2688-2698
-
-
Russell, L.J.1
Capasso, M.2
Vater, I.3
-
37
-
-
77954516863
-
Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia
-
Harvey RC, Mullighan CG, Chen IM, et al. Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia. Blood. 2010;115(26):5312-5321.
-
(2010)
Blood
, vol.115
, Issue.26
, pp. 5312-5321
-
-
Harvey, R.C.1
Mullighan, C.G.2
Chen, I.M.3
-
38
-
-
70350680415
-
Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia
-
Mullighan CG, Collins-Underwood JR, Phillips LA, et al. Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia. Nat Genet. 2009; 41(11):1243-1246.
-
(2009)
Nat Genet.
, vol.41
, Issue.11
, pp. 1243-1246
-
-
Mullighan, C.G.1
Collins-Underwood, J.R.2
Phillips, L.A.3
-
39
-
-
55249095625
-
Myeloproliferative disorders
-
Levine RL, Gilliland DG. Myeloproliferative disorders. Blood. 2008;112(6):2190-2198.
-
(2008)
Blood
, vol.112
, Issue.6
, pp. 2190-2198
-
-
Levine, R.L.1
Gilliland, D.G.2
-
40
-
-
67249146555
-
JAK mutations in high-risk childhood acute lymphoblastic leukemia
-
Mullighan CG, Zhang J, Harvey RC, et al. JAK mutations in high-risk childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA. 2009;106(23):9414-9418.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.23
, pp. 9414-9418
-
-
Mullighan, C.G.1
Zhang, J.2
Harvey, R.C.3
-
41
-
-
84868528389
-
Targeting JAK1/2 and mTOR in murine xenograft models of Ph-like acute lymphoblastic leukemia
-
Maude SL, Tasian SK, Vincent T, et al. Targeting JAK1/2 and mTOR in murine xenograft models of Ph-like acute lymphoblastic leukemia. Blood. 2012;120(17):3510-3518.
-
(2012)
Blood
, vol.120
, Issue.17
, pp. 3510-3518
-
-
Maude, S.L.1
Tasian, S.K.2
Vincent, T.3
-
42
-
-
84865118132
-
Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia
-
Roberts KG, Morin RD, Zhang J, et al. Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia. Cancer Cell. 2012; 22(2):153-166.
-
(2012)
Cancer Cell
, vol.22
, Issue.2
, pp. 153-166
-
-
Roberts, K.G.1
Morin, R.D.2
Zhang, J.3
-
43
-
-
77953193307
-
Lnk constrains myeloproliferative diseases in mice
-
Bersenev A, Wu C, Balcerek J, et al. Lnk constrains myeloproliferative diseases in mice. J Clin Invest. 2010;120(6):2058-2069.
-
(2010)
J Clin Invest.
, vol.120
, Issue.6
, pp. 2058-2069
-
-
Bersenev, A.1
Wu, C.2
Balcerek, J.3
-
44
-
-
84886513092
-
Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia
-
Weston BW, Hayden MA, Roberts KG, et al. Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia. J Clin Oncol. 2013;31(25):e413-e416.
-
(2013)
J Clin Oncol.
, vol.31
, Issue.25
, pp. e413-e416
-
-
Weston, B.W.1
Hayden, M.A.2
Roberts, K.G.3
-
45
-
-
2942563738
-
Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia
-
Harrison CJ, Moorman AV, Broadfield ZJ, et al; Childhood and Adult Leukaemia Working Parties. Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia. Br J Haematol. 2004;125(5):552-559.
-
(2004)
Br J Haematol.
, vol.125
, Issue.5
, pp. 552-559
-
-
Harrison, C.J.1
Moorman, A.V.2
Broadfield, Z.J.3
-
46
-
-
13044264463
-
Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: A report from the children's cancer group
-
Heerema NA, Nachman JB, Sather HN, et al. Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: a report from the children's cancer group. Blood. 1999;94(12): 4036-4045.
-
(1999)
Blood
, vol.94
, Issue.12
, pp. 4036-4045
-
-
Heerema, N.A.1
Nachman, J.B.2
Sather, H.N.3
-
47
-
-
0345529967
-
Reassessment of the prognostic significance of hypodiploidy in pediatric patients with acute lymphoblastic leukemia
-
Raimondi SC, Zhou Y, Mathew S, et al. Reassessment of the prognostic significance of hypodiploidy in pediatric patients with acute lymphoblastic leukemia. Cancer. 2003;98(12): 2715-2722.
-
(2003)
Cancer
, vol.98
, Issue.12
, pp. 2715-2722
-
-
Raimondi, S.C.1
Zhou, Y.2
Mathew, S.3
-
48
-
-
84874647204
-
The genomic landscape of hypodiploid acute lymphoblastic leukemia
-
Holmfeldt L, Wei L, Diaz-Flores E, et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat Genet. 2013;45(3): 242-252.
-
(2013)
Nat Genet.
, vol.45
, Issue.3
, pp. 242-252
-
-
Holmfeldt, L.1
Wei, L.2
Diaz-Flores, E.3
-
49
-
-
79957474904
-
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: A prospective observational study
-
Villani A, Tabori U, Schiffman J, et al. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study. Lancet Oncol. 2011;12(6): 559-567.
-
(2011)
Lancet Oncol.
, vol.12
, Issue.6
, pp. 559-567
-
-
Villani, A.1
Tabori, U.2
Schiffman, J.3
-
50
-
-
84876447944
-
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing
-
Powell BC, Jiang L, Muzny DM, et al. Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing. Pediatr Blood Cancer. 2013;60(6): E1-E3.
-
(2013)
Pediatr Blood Cancer
, vol.60
, Issue.6
, pp. E1-E3
-
-
Powell, B.C.1
Jiang, L.2
Muzny, D.M.3
-
51
-
-
84884999671
-
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
-
[published online ahead of print September 8, 2013]
-
Shah S, Schrader KA, Waanders E, et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia [published online ahead of print September 8, 2013]. Nat Genet.
-
Nat Genet
-
-
Shah, S.1
Schrader, K.A.2
Waanders, E.3
-
52
-
-
0027259413
-
Cytogenetically different leukemic clones at relapse of childhood acute lymphoblastic leukemia
-
Raimondi SC, Pui CH, Head DR, Rivera GK, Behm FG. Cytogenetically different leukemic clones at relapse of childhood acute lymphoblastic leukemia. Blood. 1993;82(2): 576-580.
-
(1993)
Blood
, vol.82
, Issue.2
, pp. 576-580
-
-
Raimondi, S.C.1
Pui, C.H.2
Head, D.R.3
Rivera, G.K.4
Behm, F.G.5
-
53
-
-
57149118627
-
Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia
-
Mullighan CG, Phillips LA, Su X, Ma J, Miller CB, Shurtleff SA, Downing JR. Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia. Science. 2008; 322(5906):1377-1380.
-
(2008)
Science
, vol.322
, Issue.5906
, pp. 1377-1380
-
-
Mullighan, C.G.1
Phillips, L.A.2
Su, X.3
Ma, J.4
Miller, C.B.5
Shurtleff, S.A.6
Downing, J.R.7
-
54
-
-
61549114444
-
Genomewide copy number profiling reveals molecular evolution from diagnosis to relapse in childhood acute lymphoblastic leukemia
-
Yang JJ, Bhojwani D, Yang W, et al. Genomewide copy number profiling reveals molecular evolution from diagnosis to relapse in childhood acute lymphoblastic leukemia. Blood. 2008; 112(10):4178-4183.
-
(2008)
Blood
, vol.112
, Issue.10
, pp. 4178-4183
-
-
Yang, J.J.1
Bhojwani, D.2
Yang, W.3
-
55
-
-
84864865832
-
CREBBP HAT domain mutations prevail in relapse cases of high hyperdiploid childhood acute lymphoblastic leukemia
-
Inthal A, Zeitlhofer P, Zeginigg M, et al. CREBBP HAT domain mutations prevail in relapse cases of high hyperdiploid childhood acute lymphoblastic leukemia. Leukemia. 2012;26(8): 1797-1803.
-
(2012)
Leukemia
, vol.26
, Issue.8
, pp. 1797-1803
-
-
Inthal, A.1
Zeitlhofer, P.2
Zeginigg, M.3
-
56
-
-
79952430906
-
Inactivating mutations of acetyltransferase genes in B-cell lymphoma
-
Pasqualucci L, Dominguez-Sola D, Chiarenza A, et al. Inactivating mutations of acetyltransferase genes in B-cell lymphoma. Nature. 2011; 471(7337):189-195.
-
(2011)
Nature
, vol.471
, Issue.7337
, pp. 189-195
-
-
Pasqualucci, L.1
Dominguez-Sola, D.2
Chiarenza, A.3
-
57
-
-
84874663688
-
Relapsespecific mutations in NT5C2 in childhood acute lymphoblastic leukemia
-
Meyer JA, Wang J, Hogan LE, et al. Relapsespecific mutations in NT5C2 in childhood acute lymphoblastic leukemia. Nat Genet. 2013;45(3): 290-294.
-
(2013)
Nat Genet.
, vol.45
, Issue.3
, pp. 290-294
-
-
Meyer, J.A.1
Wang, J.2
Hogan, L.E.3
-
58
-
-
84875158235
-
Activating mutations in the NT5C2 nucleotidase gene drive chemotherapy resistance in relapsed ALL
-
Tzoneva G, Perez-Garcia A, Carpenter Z, et al. Activating mutations in the NT5C2 nucleotidase gene drive chemotherapy resistance in relapsed ALL. Nat Med. 2013;19(3):368-371.
-
(2013)
Nat Med.
, vol.19
, Issue.3
, pp. 368-371
-
-
Tzoneva, G.1
Perez-Garcia, A.2
Carpenter, Z.3
-
59
-
-
79955961315
-
The 2008 WHO classification of lymphoid neoplasms and beyond: Evolving concepts and practical applications
-
Campo E, Swerdlow SH, Harris NL, Pileri S, Stein H, Jaffe ES. The 2008 WHO classification of lymphoid neoplasms and beyond: evolving concepts and practical applications. Blood. 2011; 117(19):5019-5032.
-
(2011)
Blood
, vol.117
, Issue.19
, pp. 5019-5032
-
-
Campo, E.1
Swerdlow, S.H.2
Harris, N.L.3
Pileri, S.4
Stein, H.5
Jaffe, E.S.6
-
60
-
-
84880202725
-
The genetic basis of diffuse large B-cell lymphoma
-
Pasqualucci L. The genetic basis of diffuse large B-cell lymphoma. Curr Opin Hematol. 2013; 20(4):336-344.
-
(2013)
Curr Opin Hematol.
, vol.20
, Issue.4
, pp. 336-344
-
-
Pasqualucci, L.1
-
61
-
-
75749124332
-
Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin
-
Morin RD, Johnson NA, Severson TM, et al. Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. Nat Genet. 2010;42(2): 181-185.
-
(2010)
Nat Genet.
, vol.42
, Issue.2
, pp. 181-185
-
-
Morin, R.D.1
Johnson, N.A.2
Severson, T.M.3
-
62
-
-
80052029516
-
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma
-
Morin RD, Mendez-Lago M, Mungall AJ, et al. Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma. Nature. 2011; 476(7360):298-303.
-
(2011)
Nature
, vol.476
, Issue.7360
, pp. 298-303
-
-
Morin, R.D.1
Mendez-Lago, M.2
Mungall, A.J.3
-
63
-
-
80052269038
-
Analysis of the coding genome of diffuse large B-cell lymphoma
-
Pasqualucci L, Trifonov V, Fabbri G, et al. Analysis of the coding genome of diffuse large B-cell lymphoma. Nat Genet. 2011;43(9): 830-837.
-
(2011)
Nat Genet.
, vol.43
, Issue.9
, pp. 830-837
-
-
Pasqualucci, L.1
Trifonov, V.2
Fabbri, G.3
-
64
-
-
84857942952
-
Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing
-
Lohr JG, Stojanov P, Lawrence MS, et al. Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing. Proc Natl Acad Sci USA. 2012;109(10):3879-3884.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, Issue.10
, pp. 3879-3884
-
-
Lohr, J.G.1
Stojanov, P.2
Lawrence, M.S.3
-
65
-
-
84872856782
-
Genetic heterogeneity of diffuse large B-cell lymphoma
-
Zhang J, Grubor V, Love CL, et al. Genetic heterogeneity of diffuse large B-cell lymphoma. Proc Natl Acad Sci USA. 2013;110(4): 1398-1403.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, Issue.4
, pp. 1398-1403
-
-
Zhang, J.1
Grubor, V.2
Love, C.L.3
-
66
-
-
51649111684
-
Molecular subtypes of diffuse large B-cell lymphoma arise by distinct genetic pathways
-
Lenz G, Wright GW, Emre NC, et al. Molecular subtypes of diffuse large B-cell lymphoma arise by distinct genetic pathways. Proc Natl Acad Sci USA. 2008;105(36):13520-13525.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.36
, pp. 13520-13525
-
-
Lenz, G.1
Wright, G.W.2
Emre, N.C.3
-
67
-
-
73849145729
-
Chronic active B-cell-receptor signalling in diffuse large B-cell lymphoma
-
Davis RE, Ngo VN, Lenz G, et al. Chronic active B-cell-receptor signalling in diffuse large B-cell lymphoma. Nature. 2010;463(7277):88-92.
-
(2010)
Nature
, vol.463
, Issue.7277
, pp. 88-92
-
-
Davis, R.E.1
Ngo, V.N.2
Lenz, G.3
-
68
-
-
84879734857
-
Analysis of FOXO1 mutations in diffuse large B-cell lymphoma
-
Trinh DL, Scott DW, Morin RD, et al. Analysis of FOXO1 mutations in diffuse large B-cell lymphoma. Blood. 2013;121(18):3666-3674.
-
(2013)
Blood
, vol.121
, Issue.18
, pp. 3666-3674
-
-
Trinh, D.L.1
Scott, D.W.2
Morin, R.D.3
-
69
-
-
78650454078
-
Coordinated activities of wild-type plus mutant EZH2 drive tumor-associated hypertrimethylation of lysine 27 on histone H3 (H3K27) in human B-cell lymphomas
-
Sneeringer CJ, Scott MP, Kuntz KW, Knutson SK, Pollock RM, Richon VM, Copeland RA. Coordinated activities of wild-type plus mutant EZH2 drive tumor-associated hypertrimethylation of lysine 27 on histone H3 (H3K27) in human B-cell lymphomas. Proc Natl Acad Sci USA. 2010;107(49):20980-20985.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, Issue.49
, pp. 20980-20985
-
-
Sneeringer, C.J.1
Scott, M.P.2
Kuntz, K.W.3
Knutson, S.K.4
Pollock, R.M.5
Richon, V.M.6
Copeland, R.A.7
-
70
-
-
79952167230
-
Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation
-
Yap DB, Chu J, Berg T, et al. Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation. Blood. 2011;117(8):2451-2459.
-
(2011)
Blood
, vol.117
, Issue.8
, pp. 2451-2459
-
-
Yap, D.B.1
Chu, J.2
Berg, T.3
-
71
-
-
84886290682
-
Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing
-
Morin RD, Mungall K, Pleasance E, et al. Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing. Blood. 2013;122(7):1256-1265.
-
(2013)
Blood
, vol.122
, Issue.7
, pp. 1256-1265
-
-
Morin, R.D.1
Mungall, K.2
Pleasance, E.3
-
72
-
-
84861495531
-
TBL1XR1/TP63: A novel recurrent gene fusion in B-cell non-Hodgkin lymphoma
-
Scott DW, Mungall KL, Ben-Neriah S, et al. TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma. Blood. 2012; 119(21):4949-4952.
-
(2012)
Blood
, vol.119
, Issue.21
, pp. 4949-4952
-
-
Scott, D.W.1
Mungall, K.L.2
Ben-Neriah, S.3
-
73
-
-
84866392764
-
Wholegenome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma
-
Kiel MJ, Velusamy T, Betz BL, et al. Wholegenome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma. J Exp Med. 2012;209(9):1553-1565.
-
(2012)
J Exp Med.
, vol.209
, Issue.9
, pp. 1553-1565
-
-
Kiel, M.J.1
Velusamy, T.2
Betz, B.L.3
-
74
-
-
84857763426
-
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma
-
Kridel R, Meissner B, Rogic S, et al. Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Blood. 2012;119(9):1963-1971.
-
(2012)
Blood
, vol.119
, Issue.9
, pp. 1963-1971
-
-
Kridel, R.1
Meissner, B.2
Rogic, S.3
-
75
-
-
84879157224
-
The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma
-
Meissner B, Kridel R, Lim RS, et al. The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma. Blood. 2013;121(16): 3161-3164.
-
(2013)
Blood
, vol.121
, Issue.16
, pp. 3161-3164
-
-
Meissner, B.1
Kridel, R.2
Lim, R.S.3
-
76
-
-
79952816655
-
MHC class II transactivator CIITA is a recurrent gene fusion partner in lymphoid cancers
-
Steidl C, Shah SP, Woolcock BW, et al. MHC class II transactivator CIITA is a recurrent gene fusion partner in lymphoid cancers. Nature. 2011;471(7338):377-381.
-
(2011)
Nature
, vol.471
, Issue.7338
, pp. 377-381
-
-
Steidl, C.1
Shah, S.P.2
Woolcock, B.W.3
-
77
-
-
84870538715
-
The genetic landscape of mutations in Burkitt lymphoma
-
Love C, Sun Z, Jima D, et al. The genetic landscape of mutations in Burkitt lymphoma. Nat Genet. 2012;44(12):1321-1325.
-
(2012)
Nat Genet.
, vol.44
, Issue.12
, pp. 1321-1325
-
-
Love, C.1
Sun, Z.2
Jima, D.3
-
78
-
-
84870544677
-
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing
-
Richter J, Schlesner M, Hoffmann S, et al; ICGC MMML-Seq Project. Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing. Nat Genet. 2012;44(12):1316-1320.
-
(2012)
Nat Genet.
, vol.44
, Issue.12
, pp. 1316-1320
-
-
Richter, J.1
Schlesner, M.2
Hoffmann, S.3
-
79
-
-
84867051939
-
Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics
-
Schmitz R, Young RM, Ceribelli M, et al. Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics. Nature. 2012;490(7418):116-120.
-
(2012)
Nature
, vol.490
, Issue.7418
, pp. 116-120
-
-
Schmitz, R.1
Young, R.M.2
Ceribelli, M.3
-
80
-
-
84880222541
-
Genetic and epigenetic basis of chronic lymphocytic leukemia
-
Martín-Subero JI, López-Otín C, Campo E. Genetic and epigenetic basis of chronic lymphocytic leukemia. Curr Opin Hematol. 2013; 20(4):362-368.
-
(2013)
Curr Opin Hematol.
, vol.20
, Issue.4
, pp. 362-368
-
-
Martín-Subero, J.I.1
López-Otín, C.2
Campo, E.3
-
81
-
-
84855370035
-
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia
-
Wang L, Lawrence MS, Wan Y, et al. SF3B1 and other novel cancer genes in chronic lymphocytic leukemia. N Engl J Med. 2011;365(26): 2497-2506.
-
(2011)
N Engl J Med.
, vol.365
, Issue.26
, pp. 2497-2506
-
-
Wang, L.1
Lawrence, M.S.2
Wan, Y.3
-
82
-
-
79960036578
-
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
-
Puente XS, Pinyol M, Quesada V, et al. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature. 2011;475(7354):101-105.
-
(2011)
Nature
, vol.475
, Issue.7354
, pp. 101-105
-
-
Puente, X.S.1
Pinyol, M.2
Quesada, V.3
-
83
-
-
79960353160
-
Analysis of the chronic lymphocytic leukemia coding genome: Role of NOTCH1 mutational activation
-
Fabbri G, Rasi S, Rossi D, et al. Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation. J Exp Med. 2011;208(7):1389-1401.
-
(2011)
J Exp Med.
, vol.208
, Issue.7
, pp. 1389-1401
-
-
Fabbri, G.1
Rasi, S.2
Rossi, D.3
-
84
-
-
84555171449
-
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
-
Quesada V, Conde L, Villamor N, et al. Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia. Nat Genet. 2012;44(1): 47-52.
-
(2012)
Nat Genet.
, vol.44
, Issue.1
, pp. 47-52
-
-
Quesada, V.1
Conde, L.2
Villamor, N.3
-
85
-
-
84877106592
-
The genomic landscape of chronic lymphocytic leukemia: Clinical implications
-
Quesada V, Ramsay AJ, Rodríguez D, Puente XS, Campo E, López-Otín C. The genomic landscape of chronic lymphocytic leukemia: clinical implications. BMC Med. 2013;11:124.
-
(2013)
BMC Med.
, vol.11
, pp. 124
-
-
Quesada, V.1
Ramsay, A.J.2
Rodríguez, D.3
Puente, X.S.4
Campo, E.5
López-Otín, C.6
-
86
-
-
84878551940
-
POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia
-
Ramsay AJ, Quesada V, Foronda M, et al. POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia. Nat Genet. 2013;45(5): 526-530.
-
(2013)
Nat Genet.
, vol.45
, Issue.5
, pp. 526-530
-
-
Ramsay, A.J.1
Quesada, V.2
Foronda, M.3
-
87
-
-
84880310708
-
Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia
-
Ramsay AJ, Rodríguez D, Villamor N, et al. Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia. Leukemia. 2013;27(7): 1600-1603.
-
(2013)
Leukemia
, vol.27
, Issue.7
, pp. 1600-1603
-
-
Ramsay, A.J.1
Rodríguez, D.2
Villamor, N.3
-
88
-
-
84855854025
-
Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia
-
Rossi D, Rasi S, Fabbri G, et al. Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia. Blood. 2012;119(2):521-529.
-
(2012)
Blood
, vol.119
, Issue.2
, pp. 521-529
-
-
Rossi, D.1
Rasi, S.2
Fabbri, G.3
-
89
-
-
84874428346
-
Integrated mutational and cytogenetic analysis identifies new prognostic subgroups in chronic lymphocytic leukemia
-
Rossi D, Rasi S, Spina V, et al. Integrated mutational and cytogenetic analysis identifies new prognostic subgroups in chronic lymphocytic leukemia. Blood. 2013;121(8): 1403-1412.
-
(2013)
Blood
, vol.121
, Issue.8
, pp. 1403-1412
-
-
Rossi, D.1
Rasi, S.2
Spina, V.3
-
90
-
-
84874102335
-
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
-
Landau DA, Carter SL, Stojanov P, et al. Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell. 2013;152(4): 714-726.
-
(2013)
Cell
, vol.152
, Issue.4
, pp. 714-726
-
-
Landau, D.A.1
Carter, S.L.2
Stojanov, P.3
-
91
-
-
79959293462
-
BRAF mutations in hairy-cell leukemia
-
Tiacci E, Trifonov V, Schiavoni G, et al. BRAF mutations in hairy-cell leukemia. N Engl J Med. 2011;364(24):2305-2315.
-
(2011)
N Engl J Med.
, vol.364
, Issue.24
, pp. 2305-2315
-
-
Tiacci, E.1
Trifonov, V.2
Schiavoni, G.3
-
92
-
-
84868358948
-
Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms
-
Trifa AP, Popp RA, Cucuianu A, et al. Absence of BRAF V600E mutation in a cohort of 402 patients with various chronic and acute myeloid neoplasms. Leuk Lymphoma. 2012;53(12): 2496-2497.
-
(2012)
Leuk Lymphoma.
, vol.53
, Issue.12
, pp. 2496-2497
-
-
Trifa, A.P.1
Popp, R.A.2
Cucuianu, A.3
-
93
-
-
84855590382
-
The BRAF V600E mutation in hairy cell leukemia and other mature B-cell neoplasms
-
Arcaini L, Zibellini S, Boveri E, et al. The BRAF V600E mutation in hairy cell leukemia and other mature B-cell neoplasms. Blood. 2012;119(1): 188-191.
-
(2012)
Blood
, vol.119
, Issue.1
, pp. 188-191
-
-
Arcaini, L.1
Zibellini, S.2
Boveri, E.3
-
94
-
-
84883308696
-
BRAF V600E mutation-specific antibody, a sensitive diagnostic marker revealing minimal residual disease in hairy cell leukaemia
-
Akarca AU, Shende VH, Ramsay AD, et al. BRAF V600E mutation-specific antibody, a sensitive diagnostic marker revealing minimal residual disease in hairy cell leukaemia. Br J Haematol. 2013;162(6):848-851.
-
(2013)
Br J Haematol.
, vol.162
, Issue.6
, pp. 848-851
-
-
Akarca, A.U.1
Shende, V.H.2
Ramsay, A.D.3
-
95
-
-
84861417677
-
BRAF inhibition in refractory hairycell leukemia
-
Dietrich S, Glimm H, Andrulis M, von Kalle C, Ho AD, Zenz T. BRAF inhibition in refractory hairycell leukemia. N Engl J Med. 2012;366(21): 2038-2040.
-
(2012)
N Engl J Med.
, vol.366
, Issue.21
, pp. 2038-2040
-
-
Dietrich, S.1
Glimm, H.2
Andrulis, M.3
Von Kalle, C.4
Ho, A.D.5
Zenz, T.6
-
96
-
-
79951494668
-
Initial genome sequencing and analysis of multiple myeloma
-
Chapman MA, Lawrence MS, Keats JJ, et al. Initial genome sequencing and analysis of multiple myeloma. Nature. 2011;471(7339):467-472.
-
(2011)
Nature
, vol.471
, Issue.7339
, pp. 467-472
-
-
Chapman, M.A.1
Lawrence, M.S.2
Keats, J.J.3
-
97
-
-
84893803493
-
Intraclonal heterogeneity is a critical early event in the development of myeloma and precedes the development of clinical symptoms
-
[published online ahead of print July 2, 2013]
-
Walker BA, Wardell CP, Melchor L, et al. Intraclonal heterogeneity is a critical early event in the development of myeloma and precedes the development of clinical symptoms [published online ahead of print July 2, 2013]. Leukemia.
-
Leukemia
-
-
Walker, B.A.1
Wardell, C.P.2
Melchor, L.3
-
98
-
-
84865475885
-
MYD88 L265P somatic mutation in Waldenström's macroglobulinemia
-
Treon SP, Xu L, Yang G, et al. MYD88 L265P somatic mutation in Waldenström's macroglobulinemia. N Engl J Med. 2012;367(9): 826-833.
-
(2012)
N Engl J Med.
, vol.367
, Issue.9
, pp. 826-833
-
-
Treon, S.P.1
Xu, L.2
Yang, G.3
-
99
-
-
34250630491
-
Multicenter clinical trial of bortezomib in relapsed/refractory Waldenstrom's macroglobulinemia: Results of WMCTG Trial 03-248
-
Treon SP, Hunter ZR, Matous J, et al. Multicenter clinical trial of bortezomib in relapsed/refractory Waldenstrom's macroglobulinemia: results of WMCTG Trial 03-248. Clin Cancer Res. 2007; 13(11):3320-3325.
-
(2007)
Clin Cancer Res.
, vol.13
, Issue.11
, pp. 3320-3325
-
-
Treon, S.P.1
Hunter, Z.R.2
Matous, J.3
-
100
-
-
84877278637
-
Implementing personalized cancer genomics in clinical trials
-
Simon R, Roychowdhury S. Implementing personalized cancer genomics in clinical trials. Nat Rev Drug Discov. 2013;12(5):358-369.
-
(2013)
Nat Rev Drug Discov.
, vol.12
, Issue.5
, pp. 358-369
-
-
Simon, R.1
Roychowdhury, S.2
-
101
-
-
79961007031
-
CREST maps somatic structural variation in cancer genomes with base-pair resolution
-
Wang J, Mullighan CG, Easton J, et al. CREST maps somatic structural variation in cancer genomes with base-pair resolution. Nat Methods. 2011;8(8):652-654.
-
(2011)
Nat Methods
, vol.8
, Issue.8
, pp. 652-654
-
-
Wang, J.1
Mullighan, C.G.2
Easton, J.3
-
102
-
-
84887805156
-
Genetic loss of SH2B3 in acute lymphoblastic leukemia
-
[published online ahead of print August 1, 2013]
-
Perez-Garcia A, Ambesi-Impiombato A, Hadler M, et al. Genetic loss of SH2B3 in acute lymphoblastic leukemia [published online ahead of print August 1, 2013]. Blood.
-
Blood
-
-
Perez-Garcia, A.1
Ambesi-Impiombato, A.2
Hadler, M.3
-
103
-
-
69349101565
-
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
-
Papaemmanuil E, Hosking FJ, Vijayakrishnan J, et al. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat Genet. 2009;41(9): 1006-1010.
-
(2009)
Nat Genet.
, vol.41
, Issue.9
, pp. 1006-1010
-
-
Papaemmanuil, E.1
Hosking, F.J.2
Vijayakrishnan, J.3
-
104
-
-
84877969387
-
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations
-
Xu H, Yang W, Perez-Andreu V, et al. Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. J Natl Cancer Inst. 2013;105(10): 733-742.
-
(2013)
J Natl Cancer Inst.
, vol.105
, Issue.10
, pp. 733-742
-
-
Xu, H.1
Yang, W.2
Perez-Andreu, V.3
-
105
-
-
79952188025
-
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia
-
Yang JJ, Cheng C, Devidas M, et al. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nat Genet. 2011;43(3): 237-241.
-
(2011)
Nat Genet.
, vol.43
, Issue.3
, pp. 237-241
-
-
Yang, J.J.1
Cheng, C.2
Devidas, M.3
-
106
-
-
59249100224
-
Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia
-
Yang JJ, Cheng C, Yang W, et al. Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. JAMA. 2009; 301(4):393-403.
-
(2009)
JAMA
, vol.301
, Issue.4
, pp. 393-403
-
-
Yang, J.J.1
Cheng, C.2
Yang, W.3
-
107
-
-
69349091330
-
Germline genomic variants associated with childhood acute lymphoblastic leukemia
-
Treviño LR, Yang W, French D, et al. Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat Genet. 2009; 41(9):1001-1005.
-
(2009)
Nat Genet.
, vol.41
, Issue.9
, pp. 1001-1005
-
-
Treviño, L.R.1
Yang, W.2
French, D.3
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