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1
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ATR functions as a gene dosage-dependent tumor suppressor on a mismatch repair-deficient background.
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EMBO J
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2004
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1.36
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2
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Progressive immunoglobulin gene mutations in chronic lymphocytic leukemia: evidence for antigen-driven intraclonal diversification.
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Blood
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2006
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1.29
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3
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Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
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Am J Med Genet
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2002
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1.20
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4
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SET oncoprotein overexpression in B-cell chronic lymphocytic leukemia and non-Hodgkin lymphoma: a predictor of aggressive disease and a new treatment target.
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Blood
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2011
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1.18
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5
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Clinical and molecular predictors of disease severity and survival in chronic lymphocytic leukemia.
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Am J Hematol
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2007
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1.14
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6
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A genomic approach to improve prognosis and predict therapeutic response in chronic lymphocytic leukemia.
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Clin Cancer Res
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2009
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0.98
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7
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Myeloid neoplasms secondary to plasma cell myeloma: an intrinsic predisposition or therapy-related phenomenon? A clinicopathologic study of 41 cases and correlation of cytogenetic features with treatment regimens.
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Am J Clin Pathol
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2012
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0.95
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8
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Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening.
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Hum Genet
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2003
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0.94
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9
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Reduced ATR or Chk1 expression leads to chromosome instability and chemosensitization of mismatch repair-deficient colorectal cancer cells.
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Mol Biol Cell
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2009
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0.89
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10
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Genetically characterized positive control cell lines derived from residual clinical blood samples.
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Clin Chem
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2005
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0.86
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11
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Triploid mosaicism in a 45,X/69,XXY infant.
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Am J Med Genet A
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2005
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0.83
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12
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The value of fluorescence in situ hybridization and polymerase chain reaction in the diagnosis of B-cell non-Hodgkin lymphoma by fine-needle aspiration.
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Arch Pathol Lab Med
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2004
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0.81
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13
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Clinicopathologic findings in high-grade B-cell lymphomas with typical Burkitt morphologic features but lacking the MYC translocation.
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Am J Clin Pathol
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2007
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0.80
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14
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Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet-derived growth factor receptor-alpha genes in a patient with atypical chronic myeloid leukemia.
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Genes Chromosomes Cancer
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2004
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0.79
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15
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MLL duplication in a pediatric patient with B-cell lymphoblastic lymphoma.
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J Pediatr Hematol Oncol
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2012
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0.78
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16
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Donor cell leukemia in umbilical cord blood transplant patients: a case study and literature review highlighting the importance of molecular engraftment analysis.
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J Mol Diagn
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2010
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0.77
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17
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College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis.
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Genet Med
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2011
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0.77
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18
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Pelger-Huët anomaly in a child with 1q42.3-44 deletion.
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Pediatr Blood Cancer
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2006
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0.76
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19
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A single tube, four-color flow cytometry assay for evaluation of ZAP-70 and CD38 expression in chronic lymphocytic leukemia.
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Am J Clin Pathol
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2010
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0.75
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20
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Morphologic examination of sequential bone marrow biopsies after nonmyeloablative stem cell transplantation complements molecular studies of donor engraftment.
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Arch Pathol Lab Med
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2006
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0.75
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