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About
David Oscier
Author PubWeight™ 71.93
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Nat Genet
2010
7.96
2
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.
Blood
2005
6.05
3
Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation.
J Exp Med
2011
4.37
4
Eradication of minimal residual disease in B-cell chronic lymphocytic leukemia after alemtuzumab therapy is associated with prolonged survival.
J Clin Oncol
2005
4.27
5
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms.
Blood
2009
3.69
6
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms.
Nat Genet
2009
3.21
7
Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes.
Br J Haematol
2003
2.54
8
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.
Nat Genet
2010
2.45
9
Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.
Blood
2006
2.29
10
ZAP-70 methylation status is associated with ZAP-70 expression status in chronic lymphocytic leukemia.
Haematologica
2005
1.93
11
ZAP-70 expression is associated with enhanced ability to respond to migratory and survival signals in B-cell chronic lymphocytic leukemia (B-CLL).
Blood
2005
1.91
12
Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia.
Blood
2002
1.85
13
Mutation status of the residual ATM allele is an important determinant of the cellular response to chemotherapy and survival in patients with chronic lymphocytic leukemia containing an 11q deletion.
J Clin Oncol
2007
1.82
14
Mutational status of the TP53 gene as a predictor of response and survival in patients with chronic lymphocytic leukemia: results from the LRF CLL4 trial.
J Clin Oncol
2011
1.71
15
Clonal B-cell lymphocytosis exhibiting immunophenotypic features consistent with a marginal-zone origin: is this a distinct entity?
Blood
2013
1.68
16
Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha.
Blood
2005
1.64
17
Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis.
Blood
2008
1.59
18
A subset of t(11;14) lymphoma with mantle cell features displays mutated IgVH genes and includes patients with good prognosis, nonnodal disease.
Blood
2003
1.41
19
Biallelic ATM inactivation significantly reduces survival in patients treated on the United Kingdom Leukemia Research Fund Chronic Lymphocytic Leukemia 4 trial.
J Clin Oncol
2012
1.36
20
Alemtuzumab in combination with methylprednisolone is a highly effective induction regimen for patients with chronic lymphocytic leukemia and deletion of TP53: final results of the national cancer research institute CLL206 trial.
J Clin Oncol
2012
1.35
21
DLEU2, frequently deleted in malignancy, functions as a critical host gene of the cell cycle inhibitory microRNAs miR-15a and miR-16-1.
Exp Cell Res
2009
1.22
22
Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.
Blood
2010
1.21
23
The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms.
Blood
2010
1.16
24
Two main genetic pathways lead to the transformation of chronic lymphocytic leukemia to Richter syndrome.
Blood
2013
1.06
25
Distinct organization of the candidate tumor suppressor gene RFP2 in human and mouse: multiple mRNA isoforms in both species- and human-specific antisense transcript RFP2OS.
Gene
2003
1.05
26
Abnormal serum free light chain ratios are associated with poor survival and may reflect biological subgroups in patients with chronic lymphocytic leukaemia.
Br J Haematol
2008
1.05
27
Chromosomal translocations and karyotype complexity in chronic lymphocytic leukemia: a systematic reappraisal of classic cytogenetic data.
Am J Hematol
2014
1.05
28
Exome sequence read depth methods for identifying copy number changes.
Brief Bioinform
2014
1.00
29
High-throughput sequencing analysis of the chromosome 7q32 deletion reveals IRF5 as a potential tumour suppressor in splenic marginal-zone lymphoma.
Br J Haematol
2012
1.00
30
The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre-mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1.
Genes Chromosomes Cancer
2008
0.96
31
Defining the prognosis of early stage chronic lymphocytic leukaemia patients.
Br J Haematol
2011
0.96
32
ZAP-70 in B cell malignancies.
Leuk Lymphoma
2005
0.92
33
CLLU1 expression has prognostic value in chronic lymphocytic leukemia after first-line therapy in younger patients and in those with mutated IGHV genes.
Haematologica
2012
0.87
34
Immunoglobulin heavy variable (IGHV) genes and alleles: new entities, new names and implications for research and prognostication in chronic lymphocytic leukaemia.
Immunogenetics
2014
0.83
35
Cross-talk between DNA methylation and active histone modifications regulates aberrant expression of ZAP70 in CLL.
J Cell Mol Med
2012
0.82
36
The frequency of TP53 gene defects differs between chronic lymphocytic leukaemia subgroups harbouring distinct antigen receptors.
Br J Haematol
2014
0.81
37
Capillary electrophoresis-laser induced fluorescence analysis of endogenous damage in mitochondrial and genomic DNA.
Electrophoresis
2005
0.81
38
Splenic marginal-zone lymphoma: ontogeny and genetics.
Leuk Lymphoma
2014
0.80
39
A new minimal deleted region at 11q22.3 reveals the importance of interpretation of diminished FISH signals and the choice of probe for ATM deletion screening in chronic lymphocytic leukemia.
Leuk Res
2011
0.75
40
History revisited...
Br J Haematol
2003
0.75