-
1
-
-
0001639195
-
Some speculations on the myeloproliferative syndromes
-
Dameshek W. Some speculations on the myeloproliferative syndromes. Blood 1951; 6: 372-5.
-
(1951)
Blood
, vol.6
, pp. 372-375
-
-
Dameshek, W.1
-
2
-
-
84974560145
-
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
-
Arber DA, Orazi A, Hasserjian R, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 2016; 127: 2391-405.
-
(2016)
Blood
, vol.127
, pp. 2391-2405
-
-
Arber, D.A.1
Orazi, A.2
Hasserjian, R.3
-
3
-
-
84912016855
-
Modification of British Committee for Standards in Haematology diagnostic criteria for essential thrombocythaemia
-
Harrison CN, Butt N, Campbell P, et al. Modification of British Committee for Standards in Haematology diagnostic criteria for essential thrombocythaemia. Br J Haematol 2014; 167: 421-3.
-
(2014)
Br J Haematol
, vol.167
, pp. 421-423
-
-
Harrison, C.N.1
Butt, N.2
Campbell, P.3
-
4
-
-
34548152255
-
Amendment to the guideline for diagnosis and investigation of polycythaemia/ erythrocytosis
-
McMullin MF, Reilly JT, Campbell P, et al. Amendment to the guideline for diagnosis and investigation of polycythaemia/ erythrocytosis. Br J Haematol 2007; 138: 821-2.
-
(2007)
Br J Haematol
, vol.138
, pp. 821-822
-
-
McMullin, M.F.1
Reilly, J.T.2
Campbell, P.3
-
5
-
-
84912000790
-
Use of JAK inhibitors in the management of myelofibrosis: A revision of the British Committee for Standards in Haematology Guidelines for Investigation and Management of Myelofibrosis 2012
-
Reilly JT, McMullin MF, Beer PA, et al. Use of JAK inhibitors in the management of myelofibrosis: a revision of the British Committee for Standards in Haematology Guidelines for Investigation and Management of Myelofibrosis 2012. Br J Haematol 2014; 167: 418-20.
-
(2014)
Br J Haematol
, vol.167
, pp. 418-420
-
-
Reilly, J.T.1
McMullin, M.F.2
Beer, P.A.3
-
6
-
-
38049188368
-
Bone marrow pathology in essential thrombocythemia: Interobserver reliability and utility for identifying disease subtypes
-
Wilkins BS, Erber WN, Bareford D, et al. Bone marrow pathology in essential thrombocythemia: interobserver reliability and utility for identifying disease subtypes. Blood 2008; 111: 60-70.
-
(2008)
Blood
, vol.111
, pp. 60-70
-
-
Wilkins, B.S.1
Erber, W.N.2
Bareford, D.3
-
7
-
-
84902077783
-
Rethinking the diagnostic criteria of polycythemia vera
-
Barbui T, Thiele J, Vannucchi AM, Tefferi A. Rethinking the diagnostic criteria of polycythemia vera. Leukemia 2014; 28: 1191-5.
-
(2014)
Leukemia
, vol.28
, pp. 1191-1195
-
-
Barbui, T.1
Thiele, J.2
Vannucchi, A.M.3
Tefferi, A.4
-
8
-
-
84890328032
-
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2
-
Nangalia J, Massie CE, Baxter EJ, et al. Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2. N Engl J Med 2013; 369: 2391-405.
-
(2013)
N Engl J Med
, vol.369
, pp. 2391-2405
-
-
Nangalia, J.1
Massie, C.E.2
Baxter, E.J.3
-
9
-
-
84899065964
-
Clonal evolution and clinical correlates of somatic mutations in myeloproliferative neoplasms
-
Lundberg P, Karow A, Nienhold R, et al. Clonal evolution and clinical correlates of somatic mutations in myeloproliferative neoplasms. Blood 2014; 123: 2220-8.
-
(2014)
Blood
, vol.123
, pp. 2220-2228
-
-
Lundberg, P.1
Karow, A.2
Nienhold, R.3
-
10
-
-
84883742034
-
Mutations and prognosis in primary myelofibrosis
-
Vannucchi AM, Lasho TL, Guglielmelli P, et al. Mutations and prognosis in primary myelofibrosis. Leukemia 2013; 27: 1861-9.
-
(2013)
Leukemia
, vol.27
, pp. 1861-1869
-
-
Vannucchi, A.M.1
Lasho, T.L.2
Guglielmelli, P.3
-
11
-
-
85015180955
-
Targeted deep sequencing in polycythemia vera and essential thrombocythemia
-
Tefferi A, Lasho TL, Guglielmelli P, et al. Targeted deep sequencing in polycythemia vera and essential thrombocythemia. Blood Adv 2016; 1: 21-30.
-
(2016)
Blood Adv
, vol.1
, pp. 21-30
-
-
Tefferi, A.1
Lasho, T.L.2
Guglielmelli, P.3
-
12
-
-
85027988327
-
Genetic risk assessment in myeloproliferative neoplasms
-
Tefferi A, Vannucchi AM. Genetic risk assessment in myeloproliferative neoplasms. Mayo Clin Proc 2017; 92: 1283-90.
-
(2017)
Mayo Clin Proc
, vol.92
, pp. 1283-1290
-
-
Tefferi, A.1
Vannucchi, A.M.2
-
13
-
-
84928958369
-
Effect of mutation order on myeloproliferative neoplasms
-
Ortmann CA, Kent DG, Nangalia J, et al. Effect of mutation order on myeloproliferative neoplasms. N Engl J Med 2015; 372: 601-12.
-
(2015)
N Engl J Med
, vol.372
, pp. 601-612
-
-
Ortmann, C.A.1
Kent, D.G.2
Nangalia, J.3
-
14
-
-
84946237823
-
DNMT3A mutations occur early or late in patients with myeloproliferative neoplasms and mutation order influences phenotype
-
Nangalia J, Nice FL, Wedge DC, et al. DNMT3A mutations occur early or late in patients with myeloproliferative neoplasms and mutation order influences phenotype. Haematologica 2015; 100(11): e438-42.
-
(2015)
Haematologica
, vol.100
, Issue.11
, pp. e438-e442
-
-
Nangalia, J.1
Nice, F.L.2
Wedge, D.C.3
-
15
-
-
85026309285
-
Diagnosis and classification of hematologic malignancies on the basis of genetics
-
Taylor J, Xiao W, Abdel-Wahab O. Diagnosis and classification of hematologic malignancies on the basis of genetics. Blood 2017; 130: 410-23.
-
(2017)
Blood
, vol.130
, pp. 410-423
-
-
Taylor, J.1
Xiao, W.2
Abdel-Wahab, O.3
-
16
-
-
85009727770
-
Precision oncology for acute myeloid leukemia using a knowledge bank approach
-
Gerstung M, Papaemmanuil E, Martincorena I, et al. Precision oncology for acute myeloid leukemia using a knowledge bank approach. Nat Genet 2017; 49: 332-40.
-
(2017)
Nat Genet
, vol.49
, pp. 332-340
-
-
Gerstung, M.1
Papaemmanuil, E.2
Martincorena, I.3
-
17
-
-
85026405393
-
A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis
-
Passamonti F, Giorgino T, Mora B, et al. A clinical-molecular prognostic model to predict survival in patients with post polycythemia vera and post essential thrombocythemia myelofibrosis. Leukemia 2017; 31: 2726-31.
-
(2017)
Leukemia
, vol.31
, pp. 2726-2731
-
-
Passamonti, F.1
Giorgino, T.2
Mora, B.3
-
18
-
-
63449099560
-
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms
-
Jones AV, Chase A, Silver RT, et al. JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms. Nat Genet 2009; 41: 446-9.
-
(2009)
Nat Genet
, vol.41
, pp. 446-449
-
-
Jones, A.V.1
Chase, A.2
Silver, R.T.3
-
19
-
-
84927153553
-
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
-
Tapper W, Jones AV, Kralovics R, et al. Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Nat Commun 2015; 6: 6691.
-
(2015)
Nat Commun
, vol.6
, pp. 6691
-
-
Tapper, W.1
Jones, A.V.2
Kralovics, R.3
-
20
-
-
84871464519
-
Seventy-five genetic loci influencing the human red blood cell
-
van der Harst P, Zhang W, Mateo Leach I, et al. Seventy-five genetic loci influencing the human red blood cell. Nature 2012; 492: 369-75.
-
(2012)
Nature
, vol.492
, pp. 369-375
-
-
Van Der Harst, P.1
Zhang, W.2
Mateo Leach, I.3
-
21
-
-
84872621246
-
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
-
Ruark E, Snape K, Humburg P, et al. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer. Nature 2013; 493: 406-10.
-
(2013)
Nature
, vol.493
, pp. 406-410
-
-
Ruark, E.1
Snape, K.2
Humburg, P.3
-
22
-
-
84903627855
-
Exome sequencing identifies somatic gainof- function PPM1D mutations in brainstem gliomas
-
Zhang L, Chen LH, Wan H, et al. Exome sequencing identifies somatic gainof- function PPM1D mutations in brainstem gliomas. Nat Genet 2014; 46: 726-30.
-
(2014)
Nat Genet
, vol.46
, pp. 726-730
-
-
Zhang, L.1
Chen, L.H.2
Wan, H.3
-
23
-
-
84900420439
-
MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia
-
Chen C, Liu Y, Rappaport AR, et al. MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia. Cancer Cell 2014; 25: 652-65.
-
(2014)
Cancer Cell
, vol.25
, pp. 652-665
-
-
Chen, C.1
Liu, Y.2
Rappaport, A.R.3
-
24
-
-
84958162239
-
Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients
-
Cabagnols X, Favale F, Pasquier F, et al. Presence of atypical thrombopoietin receptor (MPL) mutations in triple-negative essential thrombocythemia patients. Blood 2016; 127: 333-42.
-
(2016)
Blood
, vol.127
, pp. 333-342
-
-
Cabagnols, X.1
Favale, F.2
Pasquier, F.3
-
25
-
-
84958213572
-
Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms
-
Milosevic Feenstra JD, Nivarthi H, Gisslinger H, et al. Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms. Blood 2016; 127: 325-32.
-
(2016)
Blood
, vol.127
, pp. 325-332
-
-
Milosevic Feenstra, J.D.1
Nivarthi, H.2
Gisslinger, H.3
-
26
-
-
54349086521
-
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome
-
Bercovich D, Ganmore I, Scott LM, et al. Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome. Lancet 2008; 372: 1484-92.
-
(2008)
Lancet
, vol.372
, pp. 1484-1492
-
-
Bercovich, D.1
Ganmore, I.2
Scott, L.M.3
-
27
-
-
84887219711
-
Disruption of E627 and R683 interaction is responsible for B-cell acute lymphoblastic leukemia caused by JAK2 R683G(S) mutations
-
Wu Q-Y, Guo H-Y, Li F, Li Z-Y, Zeng L-Y, Xu K-L. Disruption of E627 and R683 interaction is responsible for B-cell acute lymphoblastic leukemia caused by JAK2 R683G(S) mutations. Leuk Lymphoma 2013; 54: 2693-700.
-
(2013)
Leuk Lymphoma
, vol.54
, pp. 2693-2700
-
-
Wu, Q.-Y.1
Guo, H.-Y.2
Li, F.3
Li, Z.-Y.4
Zeng, L.-Y.5
Xu, K.-L.6
-
28
-
-
60249086789
-
Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia
-
Kearney L, Gonzalez De Castro D, Yeung J, et al. Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia. Blood 2009; 113: 646-8.
-
(2009)
Blood
, vol.113
, pp. 646-648
-
-
Kearney, L.1
Gonzalez De Castro, D.2
Yeung, J.3
-
29
-
-
84899696697
-
Germ-line JAK2 mutations in the kinase domain are responsible for hereditary thrombocytosis and are resistant to JAK2 and HSP90 inhibitors
-
Marty C, Saint-Martin C, Pecquet C, et al. Germ-line JAK2 mutations in the kinase domain are responsible for hereditary thrombocytosis and are resistant to JAK2 and HSP90 inhibitors. Blood 2014; 123: 1372-83.
-
(2014)
Blood
, vol.123
, pp. 1372-1383
-
-
Marty, C.1
Saint-Martin, C.2
Pecquet, C.3
-
30
-
-
84920024296
-
Clonal hematopoiesis and bloodcancer risk inferred from blood DNA sequence
-
Genovese G, Kähler AK, Handsaker RE, et al. Clonal hematopoiesis and bloodcancer risk inferred from blood DNA sequence. N Engl J Med 2014; 371: 2477-87.
-
(2014)
N Engl J Med
, vol.371
, pp. 2477-2487
-
-
Genovese, G.1
Kähler, A.K.2
Handsaker, R.E.3
-
31
-
-
84920053873
-
Age-related clonal hematopoiesis associated with adverse outcomes
-
Jaiswal S, Fontanillas P, Flannick J, et al. Age-related clonal hematopoiesis associated with adverse outcomes. N Engl J Med 2014; 371: 2488-98.
-
(2014)
N Engl J Med
, vol.371
, pp. 2488-2498
-
-
Jaiswal, S.1
Fontanillas, P.2
Flannick, J.3
-
32
-
-
84973879698
-
Genomic classification and prognosis in acute myeloid leukemia
-
Papaemmanuil E, Gerstung M, Bullinger L, et al. Genomic classification and prognosis in acute myeloid leukemia. N Engl J Med 2016; 374: 2209-21.
-
(2016)
N Engl J Med
, vol.374
, pp. 2209-2221
-
-
Papaemmanuil, E.1
Gerstung, M.2
Bullinger, L.3
-
33
-
-
84907346397
-
Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia
-
Malcovati L, Papaemmanuil E, Ambaglio I, et al. Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia. Blood 2014; 124: 1513-21.
-
(2014)
Blood
, vol.124
, pp. 1513-1521
-
-
Malcovati, L.1
Papaemmanuil, E.2
Ambaglio, I.3
-
34
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
Papaemmanuil E, Gerstung M, Malcovati L, et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 2013; 122: 3616-27.
-
(2013)
Blood
, vol.122
, pp. 3616-3627
-
-
Papaemmanuil, E.1
Gerstung, M.2
Malcovati, L.3
-
35
-
-
84991030262
-
The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: An analysis of 3307 cases
-
Stengel A, Kern W, Haferlach T, Meggendorfer M, Fasan A, Haferlach C. The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 cases. Leukemia 2017; 31: 705-11.
-
(2017)
Leukemia
, vol.31
, pp. 705-711
-
-
Stengel, A.1
Kern, W.2
Haferlach, T.3
Meggendorfer, M.4
Fasan, A.5
Haferlach, C.6
-
36
-
-
84865193045
-
Patterns of survival among patients with myeloproliferative neoplasms diagnosed in Sweden from 1973 to 2008: A population-based study
-
Hultcrantz M, Kristinsson SY, Andersson TM-L, et al. Patterns of survival among patients with myeloproliferative neoplasms diagnosed in Sweden from 1973 to 2008: a population-based study. J Clin Oncol 2012; 30: 2995-3001.
-
(2012)
J Clin Oncol
, vol.30
, pp. 2995-3001
-
-
Hultcrantz, M.1
Kristinsson, S.Y.2
Tm-L, A.3
-
37
-
-
84936119720
-
Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations
-
Al Assaf C, Van Obbergh F, Billiet J, et al. Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations. Haematologica 2015; 100: 893-7.
-
(2015)
Haematologica
, vol.100
, pp. 893-897
-
-
Al Assaf, C.1
Van Obbergh, F.2
Billiet, J.3
-
38
-
-
63849328927
-
New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment
-
Cervantes F, Dupriez B, Pereira A, et al. New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. Blood 2009; 113: 2895-901.
-
(2009)
Blood
, vol.113
, pp. 2895-2901
-
-
Cervantes, F.1
Dupriez, B.2
Pereira, A.3
-
39
-
-
77950352432
-
A dynamic prognostic model to predict survival in primary myelofibrosis: A study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment)
-
Passamonti F, Cervantes F, Vannucchi AM, et al. A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment). Blood 2010; 115: 1703-8.
-
(2010)
Blood
, vol.115
, pp. 1703-1708
-
-
Passamonti, F.1
Cervantes, F.2
Vannucchi, A.M.3
-
40
-
-
84865187605
-
A prognostic model to predict survival in 867 World Health Organization-defined essential thrombocythemia at diagnosis: A study by the International Working Group on Myelofibrosis Research and Treatment
-
Passamonti F, Thiele J, Girodon F, et al. A prognostic model to predict survival in 867 World Health Organization-defined essential thrombocythemia at diagnosis: a study by the International Working Group on Myelofibrosis Research and Treatment. Blood 2012; 120: 1197-201.
-
(2012)
Blood
, vol.120
, pp. 1197-1201
-
-
Passamonti, F.1
Thiele, J.2
Girodon, F.3
|