-
1
-
-
0032188805
-
The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1,612 patients entered into the MRC AML 10 trial
-
Grimwade D, Walker H, Oliver F, et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties. Blood. 1998;92(7):2322-2333. (Pubitemid 28452973)
-
(1998)
Blood
, vol.92
, Issue.7
, pp. 2322-2333
-
-
Grimwade, D.1
Walker, H.2
Oliver, F.3
Wheatley, K.4
Harrison, C.5
Harrison, G.6
Rees, J.7
Hann, I.8
Stevens, R.9
Burnett, A.10
Goldstone, A.11
-
2
-
-
0035469883
-
The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): Analysis of 1065 patients entered into the United Kingdom Medical Research Council AML 11 trial
-
Grimwade D, Walker H, Harrison G, et al. The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): analysis of 1065 patients entered into the United Kingdom Medical Research Council AML 11 trial. Blood. 2001;98(5):1312-1320.
-
(2001)
Blood
, vol.98
, Issue.5
, pp. 1312-1320
-
-
Grimwade, D.1
Walker, H.2
Harrison, G.3
-
3
-
-
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 RK, Moorman AV, 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(3):354-365.
-
(2010)
Blood
, vol.116
, Issue.3
, pp. 354-365
-
-
Grimwade, D.1
Hills, R.K.2
Moorman, A.V.3
-
4
-
-
0035135876
-
Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: A study of 90 patients
-
DOI 10.1046/j.1365-2141.2001.02511.x
-
Schoch C, Haferlach T, Haase D, et al. Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients. Br J Haematol. 2001;112(1):118-126. (Pubitemid 32151159)
-
(2001)
British Journal of Haematology
, vol.112
, Issue.1
, pp. 118-126
-
-
Schoch, C.1
Haferlach, T.2
Haase, D.3
Fonatsch, C.4
Loffler, H.5
Schlegelberger, B.6
Staib, P.7
Sauerland, M.C.8
Heinecke, A.9
Buchner, T.10
Hiddemann, W.11
-
5
-
-
19944427850
-
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
-
DOI 10.1056/NEJMoa041974
-
Falini B, Mecucci C, Tiacci E, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med. 2005;352(3):254-266. (Pubitemid 40110814)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.3
, pp. 254-266
-
-
Falini, B.1
Mecucci, C.2
Tiacci, E.3
Alcalay, M.4
Rosati, R.5
Pasqualucci, L.6
La, S.R.7
Diverio, D.8
Colombo, E.9
Santucci, A.10
Bigerna, B.11
Pacini, R.12
Pucciarini, A.13
Liso, A.14
Vignetti, M.15
Fazi, P.16
Meani, N.17
Pettirossi, V.18
Saglio, G.19
Mandelli, F.20
Lo-Coco, F.21
Pelicci, P.-G.22
Martelli, M.F.23
more..
-
6
-
-
79954448043
-
RUNX1 mutations in acute myeloid leukemia: Results from a comprehensive genetic and clinical analysis from the AML Study Group
-
Gaidzik VI, Bullinger L, Schlenk RF, et al. RUNX1 mutations in acute myeloid leukemia: results from a comprehensive genetic and clinical analysis from the AML Study Group. J Clin Oncol. 2011; 29(10):1364-1372.
-
(2011)
J Clin Oncol
, vol.29
, Issue.10
, pp. 1364-1372
-
-
Gaidzik, V.I.1
Bullinger, L.2
Schlenk, R.F.3
-
7
-
-
42949142189
-
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
-
DOI 10.1056/NEJMoa074306
-
Schlenk RF, Döhner K, Krauter J, et al. Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia. N Engl J Med. 2008;358(18):1909-1918. (Pubitemid 351620111)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.18
, pp. 1909-1918
-
-
Schlenk, R.F.1
Dohner, K.2
Krauter, J.3
Frohling, S.4
Corbacioglu, A.5
Bullinger, L.6
Habdank, M.7
Spath, D.8
Morgan, M.9
Benner, A.10
Schlegelberger, B.11
Heil, G.12
Ganser, A.13
Dohner, H.14
-
8
-
-
0036659931
-
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: Correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
-
DOI 10.1182/blood.V100.1.59
-
Schnittger S, Schoch C, Dugas M, et al. Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood. 2002;100(1):59-66. (Pubitemid 35177429)
-
(2002)
Blood
, vol.100
, Issue.1
, pp. 59-66
-
-
Schnittger, S.1
Schoch, C.2
Dugas, M.3
Kern, W.4
Staib, P.5
Wuchter, C.6
Loffler, H.7
Sauerland, C.M.8
Serve, H.9
Buchner, T.10
Haferlach, T.11
Hiddemann, W.12
-
9
-
-
28444449081
-
Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype
-
DOI 10.1182/blood-2005-06-2248
-
Schnittger S, Schoch C, Kern W, et al. Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. Blood. 2005;106(12):3733-3739. (Pubitemid 41739006)
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3733-3739
-
-
Schnittger, S.1
Schoch, C.2
Kern, W.3
Mecucci, C.4
Tschulik, C.5
Martelli, M.F.6
Haferlach, T.7
Hiddemann, W.8
Falini, B.9
-
10
-
-
79952134550
-
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
-
Schnittger S, Dicker F, Kern W, et al. RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis. Blood. 2011;117(8):2348-2357.
-
(2011)
Blood
, vol.117
, Issue.8
, pp. 2348-2357
-
-
Schnittger, S.1
Dicker, F.2
Kern, W.3
-
11
-
-
84857699307
-
Acquired mutations in ASXL1 in acute myeloid leukemia: Prevalence and prognostic value
-
Pratcorona M, Abbas S, Sanders MA, et al. Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value. Haematologica. 2012;97(3):388-392.
-
(2012)
Haematologica
, vol.97
, Issue.3
, pp. 388-392
-
-
Pratcorona, M.1
Abbas, S.2
Sanders, M.A.3
-
12
-
-
84255176496
-
ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN favorable genetic category
-
Metzeler KH, Becker H, Maharry K, et al. ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN favorable genetic category. Blood. 2011;118(26):6920-6929.
-
(2011)
Blood
, vol.118
, Issue.26
, pp. 6920-6929
-
-
Metzeler, K.H.1
Becker, H.2
Maharry, K.3
-
13
-
-
79952122978
-
Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: Further evidence for CEBPA double mutant AML as a distinctive disease entity
-
Taskesen E, Bullinger L, Corbacioglu A, et al. Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: further evidence for CEBPA double mutant AML as a distinctive disease entity. Blood. 2011;117(8):2469-2475.
-
(2011)
Blood
, vol.117
, Issue.8
, pp. 2469-2475
-
-
Taskesen, E.1
Bullinger, L.2
Corbacioglu, A.3
-
14
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau F, Dupont S, Della V, et al. Mutation in TET2 in myeloid cancers. N Engl J Med. 2009;360(22):2289-2301.
-
(2009)
N Engl J Med
, vol.360
, Issue.22
, pp. 2289-2301
-
-
Delhommeau, F.1
Dupont, S.2
Della, V.3
-
15
-
-
83055161507
-
Wholeexome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype
-
Grossmann V, Tiacci E, Holmes AB, et al. Wholeexome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype. Blood. 2011;118(23):6153-6163.
-
(2011)
Blood
, vol.118
, Issue.23
, pp. 6153-6163
-
-
Grossmann, V.1
Tiacci, E.2
Holmes, A.B.3
-
16
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley TJ, Ding L, Walter MJ, et al. DNMT3A mutations in acute myeloid leukemia. N Engl J Med. 2010;363(25):2424-2433.
-
(2010)
N Engl J Med
, vol.363
, Issue.25
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
-
17
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med. 2009;361(11):1058- 1066.
-
(2009)
N Engl J Med
, vol.361
, Issue.11
, pp. 1058-1066
-
-
Mardis, E.R.1
Ding, L.2
Dooling, D.J.3
-
18
-
-
77449159028
-
Diagnosis and management of acute myeloid leukemia in adults: Recommendations from an international expert panel, on behalf of the European Leukemia-Net
-
Do&diehner H, Estey EH, Amadori S, et al. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European Leukemia-Net. Blood. 2010;115(3):453-474.
-
(2010)
Blood
, vol.115
, Issue.3
, pp. 453-474
-
-
Dodiehner, H.1
Estey, E.H.2
Amadori, S.3
-
20
-
-
84867808556
-
Evaluation of the new genetic risk classification of the European LeukemiaNet recommendations in 1,110 patients with de novo AML and proposal of a refined version
-
abstract. Abstract 413
-
Alpermann T, Kern W, Schnittger S, Haferlach C, Haferlach T. Evaluation of the new genetic risk classification of the European LeukemiaNet recommendations in 1,110 patients with de novo AML and proposal of a refined version [abstract]. Blood (ASH Annual Meeting Abstracts). 2012;118(21):Abstract 413.
-
(2012)
Blood (ASH Annual Meeting Abstracts)
, vol.118
, Issue.21
-
-
Alpermann, T.1
Kern, W.2
Schnittger, S.3
Haferlach, C.4
Haferlach, T.5
-
21
-
-
77956237515
-
Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1
-
Kohlmann A, Grossmann V, Klein HU, et al. Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1. J Clin Oncol. 2010;28(24):3858-3865.
-
(2010)
J Clin Oncol
, vol.28
, Issue.24
, pp. 3858-3865
-
-
Kohlmann, A.1
Grossmann, V.2
Klein, H.U.3
-
22
-
-
83555166249
-
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: A deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories
-
Kohlmann A, Klein HU, Weissmann S, et al. The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories. Leukemia. 2011;25(12):1840-1848.
-
(2011)
Leukemia
, vol.25
, Issue.12
, pp. 1840-1848
-
-
Kohlmann, A.1
Klein, H.U.2
Weissmann, S.3
-
23
-
-
49349140725
-
Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype
-
Haferlach C, Dicker F, Herholz H, et al. Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype. Leukemia. 2008;22(8):1539-1541.
-
(2008)
Leukemia
, vol.22
, Issue.8
, pp. 1539-1541
-
-
Haferlach, C.1
Dicker, F.2
Herholz, H.3
-
24
-
-
84857734093
-
TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome
-
Rucker FG, Schlenk RF, Bullinger L, et al. TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. Blood. 2012;119(9):2114-2121.
-
(2012)
Blood
, vol.119
, Issue.9
, pp. 2114-2121
-
-
Rucker, F.G.1
Schlenk, R.F.2
Bullinger, L.3
-
25
-
-
0345104178
-
Double induction strategy for acute myeloid leukemia: The effect of high-dose cytarabine with mitoxantrone instead of standard-dose cytarabine with daunorubicin and 6-thioguanine: A randomized trial by the German AML Cooperative Group
-
Buchner T, Hiddemann W, Wormann B, et al. Double induction strategy for acute myeloid leukemia: the effect of high-dose cytarabine with mitoxantrone instead of standard-dose cytarabine with daunorubicin and 6-thioguanine: a randomized trial by the German AML Cooperative Group. Blood. 1999;93(12):4116-4124. (Pubitemid 29279253)
-
(1999)
Blood
, vol.93
, Issue.12
, pp. 4116-4124
-
-
Buchner, T.1
Hiddemann, W.2
Wormann, B.3
Loffler, H.4
Gassmann, W.5
Haferlach, T.6
Fonatsch, C.7
Haase, D.8
Schoch, C.9
Hossfeld, D.10
Lengfelder, E.11
Aul, C.12
Heyll, A.13
Maschmeyer, G.14
Ludwig, W.-D.15
Sauerland, M.-C.16
Heinecke, A.17
-
26
-
-
79960118884
-
Cytarabine dose of 36 g/m(2) compared with 12 g/m(2) within first consolidation in acute myeloid leukemia: Results of patients enrolled onto the prospective randomized AML96 study
-
Schaich M, Rollig C, Soucek S, et al. Cytarabine dose of 36 g/m(2) compared with 12 g/m(2) within first consolidation in acute myeloid leukemia: results of patients enrolled onto the prospective randomized AML96 study. J Clin Oncol. 2011;29(19):2696-2702.
-
(2011)
J Clin Oncol
, vol.29
, Issue.19
, pp. 2696-2702
-
-
Schaich, M.1
Rollig, C.2
Soucek, S.3
-
27
-
-
85009854501
-
Comparison of chromosome banding analysis, interphase- and hypermetaphase-FISH, qualitative and quantitative PCR for diagnosis and for follow-up in chronic myeloid leukemia: A study on 350 cases
-
DOI 10.1038/sj/leu/2402329
-
Schoch C, Schnittger S, Bursch S, et al. Comparison of chromosome banding analysis, interphase- and hypermetaphase-FISH, qualitative and quantitative PCR for diagnosis and for follow-up in chronic myeloid leukemia: a study on 350 cases. Leukemia. 2002;16(1):53-59. (Pubitemid 34105599)
-
(2002)
Leukemia
, vol.16
, Issue.1
, pp. 53-59
-
-
Schoch, C.1
Schnittger, S.2
Bursch, S.3
Gerstner, D.4
Hochhaus, A.5
Berger, U.6
Hehlmann, R.7
Hiddemann, W.8
Haferlach, T.9
-
28
-
-
0036022067
-
Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: A detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH
-
DOI 10.1002/gcc.10088
-
Schoch C, Haferlach T, Bursch S, et al. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH. Genes Chromosomes Cancer. 2002;35(1):20-29. (Pubitemid 34847865)
-
(2002)
Genes Chromosomes and Cancer
, vol.35
, Issue.1
, pp. 20-29
-
-
Schoch, C.1
Haferlach, T.2
Bursch, S.3
Gerstner, D.4
Schnittger, S.5
Dugas, M.6
Kern, W.7
Loffler, H.8
Hiddemann, W.9
-
29
-
-
0034097609
-
Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML
-
Schnittger S, Kinkelin U, Schoch C, et al. Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML. Leukemia. 2000;14(5):796-804. (Pubitemid 30235055)
-
(2000)
Leukemia
, vol.14
, Issue.5
, pp. 796-804
-
-
Schnittger, S.1
Kinkelin, U.2
Schoch, C.3
Heinecke, A.4
Haase, D.5
Haferlach, T.6
Buchner, T.7
Wormann, B.8
Hiddemann, W.9
Griesinger, F.10
-
30
-
-
70349579540
-
Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML
-
Schnittger S, Kern W, Tschulik C, et al. Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. Blood. 2009;114(11):2220-2231.
-
(2009)
Blood
, vol.114
, Issue.11
, pp. 2220-2231
-
-
Schnittger, S.1
Kern, W.2
Tschulik, C.3
-
31
-
-
34548044732
-
Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia
-
DOI 10.1182/blood-2007-02-072595
-
Dicker F, Haferlach C, Kern W, Haferlach T, Schnittger S. Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia. Blood. 2007;110(4):1308-1316. (Pubitemid 47281430)
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1308-1316
-
-
Dicker, F.1
Haferlach, C.2
Kern, W.3
Haferlach, T.4
Schnittger, S.5
-
32
-
-
78650214949
-
A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: An analysis in 1135 patients with AML and 187 healthy controls
-
Schnittger S, Bacher U, Eder C, et al. A copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controls. Exp Hematol. 2011;39(1):87-94.
-
(2011)
Exp Hematol
, vol.39
, Issue.1
, pp. 87-94
-
-
Schnittger, S.1
Bacher, U.2
Eder, C.3
-
33
-
-
84867782129
-
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an extremely poor outcome
-
abstract. Abstract 416
-
Schnittger S, Eder C, Alpermann T, et al. ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an extremely poor outcome [abstract]. Blood (ASH Annual Meeting Abstracts). 2011;118(21):Abstract 416.
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
, Issue.21
-
-
Schnittger, S.1
Eder, C.2
Alpermann, T.3
-
34
-
-
79952451556
-
A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases
-
Grossmann V, Kohlmann A, Zenger M, et al. A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases. Leukemia. 2011;25(3):557-560.
-
(2011)
Leukemia
, vol.25
, Issue.3
, pp. 557-560
-
-
Grossmann, V.1
Kohlmann, A.2
Zenger, M.3
-
35
-
-
79952254129
-
Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology
-
Grossmann V, Schnittger S, Schindela S, et al. Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology. J Mol Diagn. 2011;13(2):129-136.
-
(2011)
J Mol Diagn
, vol.13
, Issue.2
, pp. 129-136
-
-
Grossmann, V.1
Schnittger, S.2
Schindela, S.3
-
36
-
-
77957771067
-
IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status
-
Schnittger S, Haferlach C, Ulke M, et al. IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status. Blood. 2010;116(25):5486-5496.
-
(2010)
Blood
, vol.116
, Issue.25
, pp. 5486-5496
-
-
Schnittger, S.1
Haferlach, C.2
Ulke, M.3
-
37
-
-
84860703461
-
Landscape of TET2 mutations in acute myeloid leukemia
-
Weissmann S, Alpermann T, Grossmann V, et al. Landscape of TET2 mutations in acute myeloid leukemia. Leukemia. 2012;26(5):934-942.
-
(2012)
Leukemia
, vol.26
, Issue.5
, pp. 934-942
-
-
Weissmann, S.1
Alpermann, T.2
Grossmann, V.3
-
38
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7(4):248-249.
-
(2010)
Nat Methods
, vol.7
, Issue.4
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
-
39
-
-
84863393263
-
Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
-
Patel JP, Gonen M, Figueroa ME, et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med. 2012;366(12):1079- 1089.
-
(2012)
N Engl J Med
, vol.366
, Issue.12
, pp. 1079-1089
-
-
Patel, J.P.1
Gonen, M.2
Figueroa, M.E.3
-
40
-
-
79953090055
-
Towards individualized follow-up in adult acute myeloid leukemia in remission
-
Hokland P, Ommen HB. Towards individualized follow-up in adult acute myeloid leukemia in remission. Blood. 2011;117(9):2577-2584.
-
(2011)
Blood
, vol.117
, Issue.9
, pp. 2577-2584
-
-
Hokland, P.1
Ommen, H.B.2
-
41
-
-
79960127726
-
Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia: A study from the German-Austrian acute myeloid leukemia study group
-
Kronke J, Schlenk RF, Jensen KO, et al. Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia: a study from the German-Austrian acute myeloid leukemia study group. J Clin Oncol. 2011;29(19):2709-2716.
-
(2011)
J Clin Oncol
, vol.29
, Issue.19
, pp. 2709-2716
-
-
Kronke, J.1
Schlenk, R.F.2
Jensen, K.O.3
-
42
-
-
75649091203
-
Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemias
-
Ommen HB, Schnittger S, Jovanovic JV, et al. Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemias. Blood. 2010;115(2):198-205.
-
(2010)
Blood
, vol.115
, Issue.2
, pp. 198-205
-
-
Ommen, H.B.1
Schnittger, S.2
Jovanovic, J.V.3
-
43
-
-
2642511275
-
FLT3 length mutations as marker for follow-up studies in acute myeloid leukaemia
-
DOI 10.1159/000077561
-
Schnittger S, Schoch C, Kern W, Hiddemann W, Haferlach T. FLT3 length mutations as marker for follow-up studies in acute myeloid leukaemia. Acta Haematol. 2004;112(1-2):68-78. (Pubitemid 38716251)
-
(2004)
Acta Haematologica
, vol.112
, Issue.1-2
, pp. 68-78
-
-
Schnittger, S.1
Schoch, C.2
Kern, W.3
Hiddemann, W.4
Haferlach, T.5
-
44
-
-
84873080329
-
Applicability of DHPLC for low sensitive residual disease detection in RUNX1 and CEBPA mutated AML
-
abstract. Abstract 3067
-
Schnittger S, Dicker F, Sundermann J, et al. Applicability of DHPLC for low sensitive residual disease detection in RUNX1 and CEBPA mutated AML [abstract]. Blood (ASH Annual Meeting Abstracts). 2009;114(111):Abstract 3067.
-
(2009)
Blood (ASH Annual Meeting Abstracts)
, vol.114
, Issue.111
-
-
Schnittger, S.1
Dicker, F.2
Sundermann, J.3
-
45
-
-
84872147611
-
DNMT3A mutations predict for inferior outcome in NPM1- Wildtype and molecular unfavorable cytogenetically-normal acute myeloid leukemia: A study of the German-Austrian AMLSG
-
abstract. Abstract 415
-
Gaidzik VI, Schlenk R, Paschka P, et al. DNMT3A mutations predict for inferior outcome in NPM1- wildtype and molecular unfavorable cytogenetically-normal acute myeloid leukemia: a study of the German-Austrian AMLSG [abstract]. Blood (ASH Annual Meeting Abstracts). 2011;118(21):Abstract 415.
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
, Issue.21
-
-
Gaidzik, V.I.1
Schlenk, R.2
Paschka, P.3
-
46
-
-
77957192661
-
Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: Prevalence and prognostic value
-
Abbas S, Lugthart S, Kavelaars FG, et al. Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: prevalence and prognostic value. Blood. 2010;116(12):2122-2126.
-
(2010)
Blood
, vol.116
, Issue.12
, pp. 2122-2126
-
-
Abbas, S.1
Lugthart, S.2
Kavelaars, F.G.3
-
47
-
-
77956050251
-
Prognostic impact of IDH2 mutations in cytogenetically normal acute myeloid leukemia
-
Thol F, Damm F, Wagner K, et al. Prognostic impact of IDH2 mutations in cytogenetically normal acute myeloid leukemia. Blood. 2010;116(4):614-616.
-
(2010)
Blood
, vol.116
, Issue.4
, pp. 614-616
-
-
Thol, F.1
Damm, F.2
Wagner, K.3
-
48
-
-
84862266735
-
TET2 mutations in acute myeloid leukemia (AML): Results from a comprehensive genetic and clinical analysis of the AML Study Group
-
Gaidzik VI, Paschka P, Spath D, et al. TET2 mutations in acute myeloid leukemia (AML): results from a comprehensive genetic and clinical analysis of the AML Study Group. J Clin Oncol. 2012;30(12):1350-1357.
-
(2012)
J Clin Oncol
, vol.30
, Issue.12
, pp. 1350-1357
-
-
Gaidzik, V.I.1
Paschka, P.2
Spath, D.3
-
49
-
-
79954428737
-
TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia: A Cancer and Leukemia Group B Study
-
Metzeler KH, Maharry K, Radmacher MD, et al. TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia: a Cancer and Leukemia Group B Study. J Clin Oncol. 2011;29(10):1373-1381.
-
(2011)
J Clin Oncol
, vol.29
, Issue.10
, pp. 1373-1381
-
-
Metzeler, K.H.1
Maharry, K.2
Radmacher, M.D.3
-
50
-
-
84873083385
-
ASXL1 mutations predict for resistance to chemotherapy and inferior outcome in younger adult patients with acute myeloid leukemia (AML): A study of the German-Austrian AMLSG
-
abstract. Abstract 412
-
Paschka P, Schlenk RF, Herzig J, et al. ASXL1 mutations predict for resistance to chemotherapy and inferior outcome in younger adult patients with acute myeloid leukemia (AML): a study of the German-Austrian AMLSG [abstract]. Blood (ASH Annual Meeting Abstracts). 2011;118(21):Abstract 412.
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
, Issue.21
-
-
Paschka, P.1
Schlenk, R.F.2
Herzig, J.3
-
51
-
-
63849241865
-
Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome
-
Wouters BJ, Lowenberg B, Erpelinck- Verschueren CA, et al. Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome. Blood. 2009;113(13):3088-3091.
-
(2009)
Blood
, vol.113
, Issue.13
, pp. 3088-3091
-
-
Wouters, B.J.1
Lowenberg, B.2
Erpelinck- Verschueren, C.A.3
-
52
-
-
0038208034
-
Comparative analysis of MLL partial tandem duplication and FLT3 internal tandem duplication mutations in 956 adult patients with acute myeloid leukemia
-
DOI 10.1002/gcc.10219
-
Steudel C, Wermke M, Schaich M, et al. Comparative analysis of MLL partial tandem duplication and FLT3 internal tandem duplication mutations in 956 adult patients with acute myeloid leukemia. Genes Chromosomes Cancer. 2003;37(3):237-251. (Pubitemid 36667562)
-
(2003)
Genes Chromosomes and Cancer
, vol.37
, Issue.3
, pp. 237-251
-
-
Steudel, C.1
Wermke, M.2
Schaich, M.3
Schakel, U.4
Illmer, T.5
Ehninger, G.6
Thiede, C.7
-
53
-
-
0036682174
-
Prognostic significance of partial tandem duplications of the MLL gene in adult patients 16 to 60 years old with acute myeloid leukemia and normal cytogenetics: A study of the Acute Myeloid Leukemia Study Group Ulm
-
DOI 10.1200/JCO.2002.09.088
-
Döhner K, Tobis K, Ulrich R, et al. Prognostic significance of partial tandem duplications of the MLL gene in adult patients 16 to 60 years old with acute myeloid leukemia and normal cytogenetics: a study of the Acute Myeloid Leukemia Study Group Ulm. J Clin Oncol. 2002;20(15):3254-3261. (Pubitemid 34831523)
-
(2002)
Journal of Clinical Oncology
, vol.20
, Issue.15
, pp. 3254-3261
-
-
Dohner, K.1
Tobis, K.2
Ulrich, R.3
Frohling, S.4
Benner, A.5
Schlenk, R.F.6
Dohner, H.7
-
54
-
-
84858638813
-
Profiles in leukemia
-
Godley LA. Profiles in leukemia. N Engl J Med. 2012;366(12):1152-1153.
-
(2012)
N Engl J Med
, vol.366
, Issue.12
, pp. 1152-1153
-
-
Godley, L.A.1
-
55
-
-
84867808559
-
Monitoring of minimal residual disease using next-generation deep-sequencing in 460 acute myeloid leukemia cases identifies RUNX1 mutated patients with resistant disease
-
abstract. Abstract 747
-
Kohlmann A, Grossmann V, Harbich S, et al. Monitoring of minimal residual disease using next-generation deep-sequencing in 460 acute myeloid leukemia cases identifies RUNX1 mutated patients with resistant disease [abstract]. Blood (ASH Annual Meeting Abstracts). 2011;118(21):Abstract 747.
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
, Issue.21
-
-
Kohlmann, A.1
Grossmann, V.2
Harbich, S.3
-
56
-
-
84860675045
-
Next-generation sequencing for minimal residual disease monitoring in acute myeloid leukemia patients with FLT3-ITD or NPM1 mutations
-
Thol F, Kolking B, Damm F, et al. Next-generation sequencing for minimal residual disease monitoring in acute myeloid leukemia patients with FLT3-ITD or NPM1 mutations. Genes Chromosomes Cancer. 2012;51(7):689-695.
-
(2012)
Genes Chromosomes Cancer
, vol.51
, Issue.7
, pp. 689-695
-
-
Thol, F.1
Kolking, B.2
Damm, F.3
|