Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.
|
Cancer Cell
|
2005
|
17.41
|
2
|
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia.
|
Nature
|
2012
|
9.89
|
3
|
Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants.
|
Gastroenterology
|
2005
|
3.90
|
4
|
Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia.
|
Nat Genet
|
2007
|
3.48
|
5
|
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
|
Nat Genet
|
2012
|
2.64
|
6
|
Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness.
|
Blood
|
2003
|
2.61
|
7
|
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.
|
Nat Genet
|
2007
|
2.55
|
8
|
Efficacy of the kinase inhibitor SU11248 against gastrointestinal stromal tumor mutants refractory to imatinib mesylate.
|
Clin Cancer Res
|
2006
|
2.23
|
9
|
The small molecule tyrosine kinase inhibitor AMN107 inhibits TEL-PDGFRbeta and FIP1L1-PDGFRalpha in vitro and in vivo.
|
Blood
|
2005
|
2.14
|
10
|
The FIP1L1-PDGFRalpha fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: implications for diagnosis, classification, and management.
|
Blood
|
2003
|
2.09
|
11
|
The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia.
|
Blood
|
2008
|
1.95
|
12
|
Meta-analysis of neuroblastomas reveals a skewed ALK mutation spectrum in tumors with MYCN amplification.
|
Clin Cancer Res
|
2010
|
1.79
|
13
|
Atonal homolog 1 is a tumor suppressor gene.
|
PLoS Biol
|
2009
|
1.76
|
14
|
In vitro validation of gamma-secretase inhibitors alone or in combination with other anti-cancer drugs for the treatment of T-cell acute lymphoblastic leukemia.
|
Haematologica
|
2008
|
1.69
|
15
|
Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia.
|
Nat Genet
|
2010
|
1.68
|
16
|
CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy.
|
Blood
|
2003
|
1.63
|
17
|
Genetic insights in the pathogenesis of T-cell acute lymphoblastic leukemia.
|
Haematologica
|
2005
|
1.43
|
18
|
Activation of FIP1L1-PDGFRalpha requires disruption of the juxtamembrane domain of PDGFRalpha and is FIP1L1-independent.
|
Proc Natl Acad Sci U S A
|
2006
|
1.40
|
19
|
Targeting PIM kinases impairs survival of hematopoietic cells transformed by kinase inhibitor-sensitive and kinase inhibitor-resistant forms of Fms-like tyrosine kinase 3 and BCR/ABL.
|
Cancer Res
|
2006
|
1.34
|
20
|
The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors.
|
Haematologica
|
2007
|
1.28
|
21
|
Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32).
|
Blood
|
2005
|
1.27
|
22
|
Loss or inhibition of stromal-derived PlGF prolongs survival of mice with imatinib-resistant Bcr-Abl1(+) leukemia.
|
Cancer Cell
|
2011
|
1.27
|
23
|
Potentiation of antileukemic therapies by Smac mimetic, LBW242: effects on mutant FLT3-expressing cells.
|
Mol Cancer Ther
|
2007
|
1.18
|
24
|
MOHITO, a novel mouse cytokine-dependent T-cell line, enables studies of oncogenic signaling in the T-cell context.
|
Haematologica
|
2010
|
1.16
|
25
|
Activity of dasatinib, a dual SRC/ABL kinase inhibitor, and IPI-504, a heat shock protein 90 inhibitor, against gastrointestinal stromal tumor-associated PDGFRAD842V mutation.
|
Clin Cancer Res
|
2008
|
1.16
|
26
|
Molecular mechanisms underlying FIP1L1-PDGFRA-mediated myeloproliferation.
|
Cancer Res
|
2007
|
1.15
|
27
|
ALK-positive large B-cell lymphomas with cryptic SEC31A-ALK and NPM1-ALK fusions.
|
Haematologica
|
2010
|
1.14
|
28
|
Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518.
|
Blood
|
2004
|
1.13
|
29
|
Sorafenib is a potent inhibitor of FIP1L1-PDGFRalpha and the imatinib-resistant FIP1L1-PDGFRalpha T674I mutant.
|
Blood
|
2006
|
1.10
|
30
|
The kinase inhibitor TKI258 is active against the novel CUX1-FGFR1 fusion detected in a patient with T-lymphoblastic leukemia/lymphoma and t(7;8)(q22;p11).
|
Haematologica
|
2011
|
1.10
|
31
|
JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphoma.
|
Blood
|
2011
|
1.09
|
32
|
High accuracy mutation detection in leukemia on a selected panel of cancer genes.
|
PLoS One
|
2012
|
1.08
|
33
|
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation.
|
Hum Mutat
|
2008
|
1.07
|
34
|
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA.
|
Gastroenterology
|
2006
|
1.03
|
35
|
Novel approaches to therapy of hypereosinophilic syndromes.
|
Immunol Allergy Clin North Am
|
2007
|
1.01
|
36
|
Mutation of the receptor tyrosine phosphatase PTPRC (CD45) in T-cell acute lymphoblastic leukemia.
|
Blood
|
2012
|
1.01
|
37
|
Antileukemic effects of the novel, mutant FLT3 inhibitor NVP-AST487: effects on PKC412-sensitive and -resistant FLT3-expressing cells.
|
Blood
|
2008
|
1.01
|
38
|
Kinase activation and transformation by NUP214-ABL1 is dependent on the context of the nuclear pore.
|
Mol Cell
|
2008
|
0.98
|
39
|
The fusion proteins TEL-PDGFRbeta and FIP1L1-PDGFRalpha escape ubiquitination and degradation.
|
Haematologica
|
2009
|
0.96
|
40
|
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusion.
|
Haematologica
|
2008
|
0.96
|
41
|
PTPN2 negatively regulates oncogenic JAK1 in T-cell acute lymphoblastic leukemia.
|
Blood
|
2011
|
0.94
|
42
|
Uniform sensitivity of FLT3 activation loop mutants to the tyrosine kinase inhibitor midostaurin.
|
Blood
|
2007
|
0.92
|
43
|
Genetic and epigenetic studies offer new therapeutic options for the treatment of T-cell acute lymphoblastic leukemia.
|
Haematologica
|
2012
|
0.90
|
44
|
Cancer: Mutations close in on gene regulation.
|
Nature
|
2013
|
0.90
|
45
|
Identification of protein tyrosine kinases with oncogenic potential using a retroviral insertion mutagenesis screen.
|
Haematologica
|
2009
|
0.89
|
46
|
Mutation analysis of the tyrosine phosphatase PTPN2 in Hodgkin's lymphoma and T-cell non-Hodgkin's lymphoma.
|
Haematologica
|
2011
|
0.87
|
47
|
A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
|
Genes Chromosomes Cancer
|
2003
|
0.87
|
48
|
Cellular transformation of NIH3T3 fibroblasts by CIZ/NMP4 fusions.
|
J Cell Biochem
|
2005
|
0.86
|
49
|
G-749, a novel FLT3 kinase inhibitor, can overcome drug resistance for the treatment of acute myeloid leukemia.
|
Blood
|
2014
|
0.86
|
50
|
Improvements in the survival of children and adolescents with acute lymphoblastic leukemia.
|
Haematologica
|
2012
|
0.86
|
51
|
JAK1 mutation analysis in T-cell acute lymphoblastic leukemia cell lines.
|
Haematologica
|
2009
|
0.85
|
52
|
Identification of a novel, recurrent MBTD1-CXorf67 fusion in low-grade endometrial stromal sarcoma.
|
Int J Cancer
|
2013
|
0.82
|
53
|
EGFR inhibition in non-small cell lung cancer: resistance, once again, rears its ugly head.
|
PLoS Med
|
2005
|
0.82
|
54
|
The N676D and G697R mutations in the kinase domain of FLT3 confer resistance to the inhibitor AC220.
|
Haematologica
|
2012
|
0.80
|
55
|
FLT1 kinase is a mediator of radioresistance and survival in head and neck squamous cell carcinoma.
|
Acta Oncol
|
2013
|
0.79
|
56
|
When splicing turns bad.
|
Haematologica
|
2012
|
0.78
|
57
|
FIP1L1-PDGFRalpha in hypereosinophilic syndrome and mastocytosis.
|
Hematol J
|
2004
|
0.78
|
58
|
Chromosomal aberrations and fusion genes in myeloid malignancies.
|
Expert Rev Hematol
|
2012
|
0.78
|
59
|
BMI1, the polycomb-group gene, is recurrently targeted by genomic rearrangements in progressive B-cell leukemia/lymphoma.
|
Genes Chromosomes Cancer
|
2013
|
0.78
|
60
|
Recent breakthroughs in the understanding and management of chronic eosinophilic leukemia.
|
Expert Rev Anticancer Ther
|
2009
|
0.78
|
61
|
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia.
|
Haematologica
|
2014
|
0.78
|
62
|
JAK3 specific kinase inhibitors: when specificity is not enough.
|
Chem Biol
|
2011
|
0.78
|
63
|
Rearrangement of NOTCH1 or BCL3 can independently trigger progression of CLL.
|
Blood
|
2012
|
0.78
|
64
|
Using the hemoglobin switch for the treatment of sickle cell disease.
|
Haematologica
|
2012
|
0.77
|
65
|
The hypereosinophilic syndrome: idiopathic or not, that is the question.
|
Haematologica
|
2005
|
0.77
|
66
|
TV6 and PDGFRB: a license to fuse.
|
Haematologica
|
2007
|
0.77
|
67
|
Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).
|
Haematologica
|
2006
|
0.76
|
68
|
Primetime for chemotherapy in acute myeloid leukemia.
|
Haematologica
|
2012
|
0.76
|
69
|
Resolutions for the New Year.
|
Haematologica
|
2016
|
0.75
|
70
|
Development of a siRNA and shRNA screening system based on a kinase fusion protein.
|
RNA
|
2012
|
0.75
|
71
|
A fly's view of the hematopoietic niche.
|
Haematologica
|
2012
|
0.75
|
72
|
New opportunities and new problems for acute myeloid leukemia treatment.
|
Haematologica
|
2012
|
0.75
|
73
|
Detection of clonal blood cells with specific chromosomal abnormalities in the general population.
|
Haematologica
|
2012
|
0.75
|
74
|
New flow cytometry in hematologic malignancies.
|
Haematologica
|
2009
|
0.75
|
75
|
Identification of novel FLT3 kinase inhibitors.
|
Eur J Med Chem
|
2013
|
0.75
|