-
1
-
-
66349104231
-
Therapy-related myeloid neoplasms
-
International Agency for Research on Cancer (IARC), Lyon, S.H. Swerdlow, E. Campo, N.L. Harris, E.S. Jaffe, S.A. Pileri, H. Stein (Eds.)
-
Vardiman J.W., Arber D.A., Brunning R.D., Larson R.A., Matutes E., Baumann I., et al. Therapy-related myeloid neoplasms. WHO classification of tumours of haematopoietic and lymphoid tissues 2008, 127-129. International Agency for Research on Cancer (IARC), Lyon. 4th ed. S.H. Swerdlow, E. Campo, N.L. Harris, E.S. Jaffe, S.A. Pileri, H. Stein (Eds.).
-
(2008)
WHO classification of tumours of haematopoietic and lymphoid tissues
, pp. 127-129
-
-
Vardiman, J.W.1
Arber, D.A.2
Brunning, R.D.3
Larson, R.A.4
Matutes, E.5
Baumann, I.6
-
2
-
-
77956870600
-
Promoter methylation of DAPK1, E-cadherin and thrombospondin-1 in de novo and therapy-related myeloid neoplasms
-
Greco M., D'Alo F., Scardocci A., Criscuolo M., Fabiani E., Guidi F., et al. Promoter methylation of DAPK1, E-cadherin and thrombospondin-1 in de novo and therapy-related myeloid neoplasms. Blood Cells, Mol, Dis 2010, 45:181-185.
-
(2010)
Blood Cells, Mol, Dis
, vol.45
, pp. 181-185
-
-
Greco, M.1
D'Alo, F.2
Scardocci, A.3
Criscuolo, M.4
Fabiani, E.5
Guidi, F.6
-
3
-
-
77950629779
-
Epigenetic changes in therapy-related MDS/AML
-
Voso M.T., D'Alo F., Greco M., Fabiani E., Criscuolo M., Migliara G., et al. Epigenetic changes in therapy-related MDS/AML. Chem-Biol Interact 2010, 184:46-49.
-
(2010)
Chem-Biol Interact
, vol.184
, pp. 46-49
-
-
Voso, M.T.1
D'Alo, F.2
Greco, M.3
Fabiani, E.4
Criscuolo, M.5
Migliara, G.6
-
5
-
-
0038305924
-
Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series
-
Smith S.M., Le Beau M.M., Huo D., Karrison T., Sobecks R.M., Anastasi J., et al. Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series. Blood 2003, 102:43-52.
-
(2003)
Blood
, vol.102
, pp. 43-52
-
-
Smith, S.M.1
Le Beau, M.M.2
Huo, D.3
Karrison, T.4
Sobecks, R.M.5
Anastasi, J.6
-
6
-
-
84856553821
-
Therapy-related myeloid neoplasms following fludarabine, cyclophosphamide, and rituximab (FCR) treatment in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma
-
Zhou Y., Tang G., Medeiros L.J., McDonnell T.J., Keating M.J., Wierda W.G., et al. Therapy-related myeloid neoplasms following fludarabine, cyclophosphamide, and rituximab (FCR) treatment in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. Mod Pathol 2012, 25:237-245.
-
(2012)
Mod Pathol
, vol.25
, pp. 237-245
-
-
Zhou, Y.1
Tang, G.2
Medeiros, L.J.3
McDonnell, T.J.4
Keating, M.J.5
Wierda, W.G.6
-
7
-
-
84891870816
-
Application of the International Prognostic Scoring System-Revised in therapy-related myelodysplastic syndromes and oligoblastic acute myeloid leukemia
-
Ok C.Y., Hasserjian R.P., Fox P.S., Stingo F., Zuo Z., Young K.H., et al. Application of the International Prognostic Scoring System-Revised in therapy-related myelodysplastic syndromes and oligoblastic acute myeloid leukemia. Leukemia 2014, 28:185-189.
-
(2014)
Leukemia
, vol.28
, pp. 185-189
-
-
Ok, C.Y.1
Hasserjian, R.P.2
Fox, P.S.3
Stingo, F.4
Zuo, Z.5
Young, K.H.6
-
8
-
-
84878900540
-
Clonal diversity of recurrently mutated genes in myelodysplastic syndromes
-
Walter M.J., Shen D., Shao J., Ding L., White B.S., Kandoth C., et al. Clonal diversity of recurrently mutated genes in myelodysplastic syndromes. Leukemia 2013, 27:1275-1282.
-
(2013)
Leukemia
, vol.27
, pp. 1275-1282
-
-
Walter, M.J.1
Shen, D.2
Shao, J.3
Ding, L.4
White, B.S.5
Kandoth, C.6
-
9
-
-
84878372012
-
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
-
Cancer Genome Atlas Research Network Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med 2013, 368:2059-2074.
-
(2013)
N Engl J Med
, vol.368
, pp. 2059-2074
-
-
-
10
-
-
84867806184
-
A novel hierarchical prognostic model of AML solely based on molecular mutations
-
Grossmann V., Schnittger S., Kohlmann A., Eder C., Roller A., Dicker F., et al. A novel hierarchical prognostic model of AML solely based on molecular mutations. Blood 2012, 120:2963-2972.
-
(2012)
Blood
, vol.120
, pp. 2963-2972
-
-
Grossmann, V.1
Schnittger, S.2
Kohlmann, A.3
Eder, C.4
Roller, A.5
Dicker, F.6
-
11
-
-
84863393263
-
Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
-
Patel J.P., Gonen M., Figueroa M.E., Fernandez H., Sun Z., Racevskis J., et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med 2012, 366:1079-1089.
-
(2012)
N Engl J Med
, vol.366
, pp. 1079-1089
-
-
Patel, J.P.1
Gonen, M.2
Figueroa, M.E.3
Fernandez, H.4
Sun, Z.5
Racevskis, J.6
-
12
-
-
84866749552
-
Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
-
Bejar R., Stevenson K.E., Caughey B.A., Abdel-Wahab O., Steensma D.P., Galili N., et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J Clin Oncol 2012, 30:3376-3382.
-
(2012)
J Clin Oncol
, vol.30
, pp. 3376-3382
-
-
Bejar, R.1
Stevenson, K.E.2
Caughey, B.A.3
Abdel-Wahab, O.4
Steensma, D.P.5
Galili, N.6
-
13
-
-
84878446656
-
Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia
-
Shih A.H., Chung S.S., Dolezal E.K., Zhang S.J., Abdel-Wahab O.I., Park C.Y., et al. Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia. Haematologica 2013, 98:908-912.
-
(2013)
Haematologica
, vol.98
, pp. 908-912
-
-
Shih, A.H.1
Chung, S.S.2
Dolezal, E.K.3
Zhang, S.J.4
Abdel-Wahab, O.I.5
Park, C.Y.6
-
14
-
-
39149093029
-
Genetics of therapy-related myelodysplasia and acute myeloid leukemia
-
Pedersen-Bjergaard J., Andersen M.K., Andersen M.T., Christiansen D.H. Genetics of therapy-related myelodysplasia and acute myeloid leukemia. Leukemia 2008, 22:240-248.
-
(2008)
Leukemia
, vol.22
, pp. 240-248
-
-
Pedersen-Bjergaard, J.1
Andersen, M.K.2
Andersen, M.T.3
Christiansen, D.H.4
-
15
-
-
84877266636
-
Updating benchtop sequencing performance comparison
-
Junemann S., Sedlazeck F.J., Prior K., Albersmeier A., John U., Kalinowski J., et al. Updating benchtop sequencing performance comparison. Nat Biotechnol 2013, 31:294-296.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 294-296
-
-
Junemann, S.1
Sedlazeck, F.J.2
Prior, K.3
Albersmeier, A.4
John, U.5
Kalinowski, J.6
-
16
-
-
78651271733
-
Integrative genomics viewer
-
Robinson J.T., Thorvaldsdottir H., Winckler W., Guttman M., Lander E.S., Getz G., et al. Integrative genomics viewer. Nat Biotechnol 2011, 29:24-26.
-
(2011)
Nat Biotechnol
, vol.29
, pp. 24-26
-
-
Robinson, J.T.1
Thorvaldsdottir, H.2
Winckler, W.3
Guttman, M.4
Lander, E.S.5
Getz, G.6
-
17
-
-
84888069767
-
OncoSeek: a versatile annotation and reporting system for next generation sequencing-based clinical mutation analysis of cancer specimens. AMP 2012 Meeting Abstract
-
Abstract TT79
-
Routbort M., Handal B., Patel K.P., Singh R., Aldape K., Reddy N., et al. OncoSeek: a versatile annotation and reporting system for next generation sequencing-based clinical mutation analysis of cancer specimens. AMP 2012 Meeting Abstract. J Mol Diagn 2012, 14:637-748. Abstract TT79.
-
(2012)
J Mol Diagn
, vol.14
, pp. 637-748
-
-
Routbort, M.1
Handal, B.2
Patel, K.P.3
Singh, R.4
Aldape, K.5
Reddy, N.6
-
18
-
-
84895770396
-
Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring
-
Luthra R., Patel K.P., Reddy N.G., Haghshenas V., Routbort M.J., Harmon M.A., et al. Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring. Haematologica 2014, 99:465-473.
-
(2014)
Haematologica
, vol.99
, pp. 465-473
-
-
Luthra, R.1
Patel, K.P.2
Reddy, N.G.3
Haghshenas, V.4
Routbort, M.J.5
Harmon, M.A.6
-
19
-
-
0142200874
-
Cytogenetic findings in blastoid mantle cell lymphoma
-
Khoury J.D., Sen F., Abruzzo L.V., Hayes K., Glassman A., Medeiros L.J. Cytogenetic findings in blastoid mantle cell lymphoma. Hum Pathol 2003, 34:1022-1029.
-
(2003)
Hum Pathol
, vol.34
, pp. 1022-1029
-
-
Khoury, J.D.1
Sen, F.2
Abruzzo, L.V.3
Hayes, K.4
Glassman, A.5
Medeiros, L.J.6
-
21
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P., Cox C., LeBeau M.M., Fenaux P., Morel P., Sanz G., et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997, 89:2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
Fenaux, P.4
Morel, P.5
Sanz, G.6
-
22
-
-
77955914238
-
Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials
-
Grimwade D., Hills R.K., Moorman A.V., Walker H., Chatters S., Goldstone A.H., et al. Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials. Blood 2010, 116:354-365.
-
(2010)
Blood
, vol.116
, pp. 354-365
-
-
Grimwade, D.1
Hills, R.K.2
Moorman, A.V.3
Walker, H.4
Chatters, S.5
Goldstone, A.H.6
-
23
-
-
84876129012
-
IDH1 and IDH2 mutations in therapy-related myelodysplastic syndrome and acute myeloid leukemia are associated with a normal karyotype and with der(1;7)(q10;p10)
-
Westman M.K., Pedersen-Bjergaard J., Andersen M.T., Andersen M.K. IDH1 and IDH2 mutations in therapy-related myelodysplastic syndrome and acute myeloid leukemia are associated with a normal karyotype and with der(1;7)(q10;p10). Leukemia 2013, 27:957-959.
-
(2013)
Leukemia
, vol.27
, pp. 957-959
-
-
Westman, M.K.1
Pedersen-Bjergaard, J.2
Andersen, M.T.3
Andersen, M.K.4
-
24
-
-
84893772765
-
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
-
Haferlach T., Nagata Y., Grossmann V., Okuno Y., Bacher U., Nagae G., et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia 2014, 28:241-247.
-
(2014)
Leukemia
, vol.28
, pp. 241-247
-
-
Haferlach, T.1
Nagata, Y.2
Grossmann, V.3
Okuno, Y.4
Bacher, U.5
Nagae, G.6
-
25
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
quiz 99
-
Papaemmanuil E., Gerstung M., Malcovati L., Tauro S., Gundem G., Van Loo P., et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 2013, 122:3616-3627. quiz 99.
-
(2013)
Blood
, vol.122
, pp. 3616-3627
-
-
Papaemmanuil, E.1
Gerstung, M.2
Malcovati, L.3
Tauro, S.4
Gundem, G.5
Van Loo, P.6
-
26
-
-
79960255863
-
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
-
Walter M.J., Ding L., Shen D., Shao J., Grillot M., McLellan M., et al. Recurrent DNMT3A mutations in patients with myelodysplastic syndromes. Leukemia 2011, 25:1153-1158.
-
(2011)
Leukemia
, vol.25
, pp. 1153-1158
-
-
Walter, M.J.1
Ding, L.2
Shen, D.3
Shao, J.4
Grillot, M.5
McLellan, M.6
-
27
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar R., Stevenson K., Abdel-Wahab O., Galili N., Nilsson B., Garcia-Manero G., et al. Clinical effect of point mutations in myelodysplastic syndromes. N Engl J Med 2011, 364:2496-2506.
-
(2011)
N Engl J Med
, vol.364
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
-
28
-
-
84859856420
-
Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
-
Thol F., Kade S., Schlarmann C., Loffeld P., Morgan M., Krauter J., et al. Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes. Blood 2012, 119:3578-3584.
-
(2012)
Blood
, vol.119
, pp. 3578-3584
-
-
Thol, F.1
Kade, S.2
Schlarmann, C.3
Loffeld, P.4
Morgan, M.5
Krauter, J.6
-
29
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M., Mehler E.L., Goldberg R., Zampino G., Brunner H.G., Kremer H., et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001, 29:465-468.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
Zampino, G.4
Brunner, H.G.5
Kremer, H.6
-
30
-
-
34247518152
-
Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations
-
Christiansen D.H., Desta F., Andersen M.K., Pedersen-Bjergaard J. Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations. Genes, Chromosomes Cancer 2007, 46:517-521.
-
(2007)
Genes, Chromosomes Cancer
, vol.46
, pp. 517-521
-
-
Christiansen, D.H.1
Desta, F.2
Andersen, M.K.3
Pedersen-Bjergaard, J.4
-
31
-
-
79952092487
-
Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications
-
Marcucci G., Haferlach T., Dohner H. Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications. J Clin Oncol 2011, 29:475-486.
-
(2011)
J Clin Oncol
, vol.29
, pp. 475-486
-
-
Marcucci, G.1
Haferlach, T.2
Dohner, H.3
-
32
-
-
84872165619
-
Mutational landscape of AML with normal cytogenetics: biological and clinical implications
-
Martelli M.P., Sportoletti P., Tiacci E., Martelli M.F., Falini B. Mutational landscape of AML with normal cytogenetics: biological and clinical implications. Blood Rev 2013, 27:13-22.
-
(2013)
Blood Rev
, vol.27
, pp. 13-22
-
-
Martelli, M.P.1
Sportoletti, P.2
Tiacci, E.3
Martelli, M.F.4
Falini, B.5
-
33
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley T.J., Ding L., Walter M.J., McLellan M.D., Lamprecht T., Larson D.E., et al. DNMT3A mutations in acute myeloid leukemia. N Engl J Med 2010, 363:2424-2433.
-
(2010)
N Engl J Med
, vol.363
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
McLellan, M.D.4
Lamprecht, T.5
Larson, D.E.6
-
34
-
-
84873381393
-
Patients with therapy-related myelodysplastic syndromes and acute myeloid leukemia share genetic features but can be separated by blast counts and cytogenetic risk profiles into prognostically relevant subgroups
-
Bacher U., Haferlach C., Alpermann T., Schnittger S., Kern W., Haferlach T. Patients with therapy-related myelodysplastic syndromes and acute myeloid leukemia share genetic features but can be separated by blast counts and cytogenetic risk profiles into prognostically relevant subgroups. Leuk Lymphoma 2013, 54:639-642.
-
(2013)
Leuk Lymphoma
, vol.54
, pp. 639-642
-
-
Bacher, U.1
Haferlach, C.2
Alpermann, T.3
Schnittger, S.4
Kern, W.5
Haferlach, T.6
|