1
|
A biologic definition of Burkitt's lymphoma from transcriptional and genomic profiling.
|
N Engl J Med
|
2006
|
7.42
|
2
|
Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia.
|
Blood
|
2009
|
3.50
|
3
|
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL).
|
Blood
|
2006
|
1.74
|
4
|
A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms.
|
PLoS One
|
2009
|
1.48
|
5
|
Diffuse large B-cell lymphoma in pediatric patients belongs predominantly to the germinal-center type B-cell lymphomas: a clinicopathologic analysis of cases included in the German BFM (Berlin-Frankfurt-Munster) Multicenter Trial.
|
Blood
|
2006
|
1.45
|
6
|
Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.
|
Int J Cancer
|
2003
|
1.41
|
7
|
Translocations activating IRF4 identify a subtype of germinal center-derived B-cell lymphoma affecting predominantly children and young adults.
|
Blood
|
2011
|
1.39
|
8
|
Recurrent involvement of the REL and BCL11A loci in classical Hodgkin lymphoma.
|
Blood
|
2002
|
1.38
|
9
|
A chromosomal translocation in cyclin D1-negative/cyclin D2-positive mantle cell lymphoma fuses the CCND2 gene to the IGK locus.
|
Blood
|
2006
|
1.25
|
10
|
Follicular lymphoma lacking the t(14;18)(q32;q21): identification of two disease subtypes.
|
Br J Haematol
|
2003
|
1.21
|
11
|
Quantitative assessment of molecular remission after high-dose therapy with autologous stem cell transplantation predicts long-term remission in mantle cell lymphoma.
|
Blood
|
2005
|
1.17
|
12
|
Multicolor-FICTION: expanding the possibilities of combined morphologic, immunophenotypic, and genetic single cell analyses.
|
Am J Pathol
|
2002
|
1.12
|
13
|
The BCR-ABL1 kinase bypasses selection for the expression of a pre-B cell receptor in pre-B acute lymphoblastic leukemia cells.
|
J Exp Med
|
2004
|
1.11
|
14
|
t(6;14)(p22;q32): a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL).
|
Blood
|
2007
|
1.10
|
15
|
Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasms.
|
Genes Chromosomes Cancer
|
2003
|
0.96
|
16
|
Chromosomal breakpoints affecting immunoglobulin loci are recurrent in Hodgkin and Reed-Sternberg cells of classical Hodgkin lymphoma.
|
Cancer Res
|
2006
|
0.96
|
17
|
Interphase FISH assays for the detection of translocations with breakpoints in immunoglobulin light chain loci.
|
Int J Cancer
|
2002
|
0.94
|
18
|
Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
|
Genomics
|
2004
|
0.94
|
19
|
Inhibition of anaplastic lymphoma kinase (ALK) activity provides a therapeutic approach for CLTC-ALK-positive human diffuse large B cell lymphomas.
|
PLoS One
|
2011
|
0.93
|
20
|
Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemia.
|
Br J Haematol
|
2007
|
0.93
|
21
|
Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B-chronic lymphocytic leukaemia.
|
Br J Haematol
|
2007
|
0.92
|
22
|
Interphase cytogenetics of hematological neoplasms under the perspective of the novel WHO classification.
|
Anticancer Res
|
2003
|
0.90
|
23
|
The CBFA2T3/ACSF3 locus is recurrently involved in IGH chromosomal translocation t(14;16)(q32;q24) in pediatric B-cell lymphoma with germinal center phenotype.
|
Genes Chromosomes Cancer
|
2012
|
0.90
|
24
|
GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma.
|
Br J Haematol
|
2008
|
0.90
|
25
|
Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtaposition.
|
Cancer Genet Cytogenet
|
2009
|
0.90
|
26
|
Common clonal T-cell origin in a patient with T-prolymphocytic leukaemia and associated cutaneous T-cell lymphomas.
|
Br J Haematol
|
2003
|
0.85
|
27
|
Deregulation of the telomerase reverse transcriptase (TERT) gene by chromosomal translocations in B-cell malignancies.
|
Blood
|
2010
|
0.84
|
28
|
Acute myeloid leukemia with deletion 9q within a noncomplex karyotype is associated with CEBPA loss-of-function mutations.
|
Genes Chromosomes Cancer
|
2005
|
0.84
|
29
|
Recurrent loss of the Y chromosome and homozygous deletions within the pseudoautosomal region 1: association with male predominance in mantle cell lymphoma.
|
Haematologica
|
2008
|
0.82
|
30
|
Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management.
|
Breast Cancer Res Treat
|
2012
|
0.82
|
31
|
Identification of the gene encoding cyclin E1 (CCNE1) as a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphoma.
|
Haematologica
|
2009
|
0.81
|
32
|
Expression of ZAP-70 protein correlates with disease stage in chronic lymphocytic leukemia and is associated with, but not generally restricted to, non-mutated Ig VH status.
|
Leuk Lymphoma
|
2004
|
0.79
|
33
|
Neuropsychological correlates of written expression in college students with ADHD.
|
J Atten Disord
|
2010
|
0.78
|
34
|
Molecular characterization of a novel chromosomal translocation t(12;14)(q23;q11.2) in T-lymphoblastic lymphoma between the T-cell receptor delta-deleting elements (TRDREC and TRAJ61) and the hypothetical gene C12orf42.
|
Eur J Haematol
|
2010
|
0.78
|
35
|
Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies.
|
Cancer Genet Cytogenet
|
2003
|
0.78
|
36
|
Studies of four new human myeloma cell lines.
|
Leuk Lymphoma
|
2005
|
0.76
|
37
|
Blastoid variant of mantle cell lymphoma: late progression from classical mantle cell lymphoma and quantitation of minimal residual disease.
|
Eur J Haematol
|
2005
|
0.75
|
38
|
Marked thrombocytosis in a child with advanced myelodysplastic syndrome.
|
Leuk Lymphoma
|
2004
|
0.75
|
39
|
Splenic infarction associated with rapidly progressive chronic lymphocytic leukemia with complex karyotype and ATM mutation.
|
Leuk Res
|
2010
|
0.75
|
40
|
The short arm of chromosome 18 is a recurrent integration site of a supernumerary BCR/ABL gene fusion in chronic myeloid leukemia.
|
Cancer Genet Cytogenet
|
2007
|
0.75
|
41
|
Pediatric multiple sclerosis: what we know and where are we headed?
|
Child Neuropsychol
|
2012
|
0.75
|