Published in J Mol Diagn on September 09, 2011
IgH partner breakpoint sequences provide evidence that AID initiates t(11;14) and t(8;14) chromosomal breaks in mantle cell and Burkitt lymphomas. Blood (2012) 0.93
Human molecular cytogenetics: From cells to nucleotides. Genet Mol Biol (2014) 0.80
Genome Fusion Detection: a novel method to detect fusion genes from SNP-array data. Bioinformatics (2013) 0.78
Evolution of genetic techniques: past, present, and beyond. Biomed Res Int (2015) 0.77
Characterization of a case of follicular lymphoma transformed into B-lymphoblastic leukemia. Mol Cytogenet (2013) 0.77
Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization. J Mol Diagn (2015) 0.75
Value of oligonucleotide-based array comparative genomic hybridization for diagnosis of acute promyelocytic leukemia in a patient negative for t(15;17)(q24.1;q21.2)/promyelocytic leukemia-retinoic acid receptor, alpha by conventional cytogenetics and fluorescence in situ hybridization. Clin Lymphoma Myeloma Leuk (2013) 0.75
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet (2008) 43.63
Recurrent fusion of TMPRSS2 and ETS transcription factor genes in prostate cancer. Science (2005) 39.06
Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature (2007) 37.09
Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc Natl Acad Sci U S A (1988) 35.13
Paired-end mapping reveals extensive structural variation in the human genome. Science (2007) 30.46
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature (2007) 17.68
Genomic aberrations and survival in chronic lymphocytic leukemia. N Engl J Med (2000) 16.30
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet (2010) 13.70
Complex landscapes of somatic rearrangement in human breast cancer genomes. Nature (2009) 13.45
Transcriptome sequencing to detect gene fusions in cancer. Nature (2009) 11.63
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature (2008) 10.12
The impact of translocations and gene fusions on cancer causation. Nat Rev Cancer (2007) 9.81
Polymerase chain reaction with single-sided specificity: analysis of T cell receptor delta chain. Science (1989) 9.01
Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer (1997) 8.27
End-sequence profiling: sequence-based analysis of aberrant genomes. Proc Natl Acad Sci U S A (2003) 7.70
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution. Genome Res (2007) 6.91
Development of personalized tumor biomarkers using massively parallel sequencing. Sci Transl Med (2010) 6.08
Methods and strategies for analyzing copy number variation using DNA microarrays. Nat Genet (2007) 5.64
Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization. J Clin Oncol (2006) 4.49
Altered nucleotide sequences of a translocated c-myc gene in Burkitt lymphoma. Nature (1984) 4.24
Frequent inactivation of A20 in B-cell lymphomas. Nature (2009) 4.22
An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science (2007) 4.00
Molecular pathogenesis and a consequent classification of multiple myeloma. J Clin Oncol (2005) 3.93
Androgen-induced TOP2B-mediated double-strand breaks and prostate cancer gene rearrangements. Nat Genet (2010) 3.83
Human chromosomal translocations at CpG sites and a theoretical basis for their lineage and stage specificity. Cell (2008) 3.31
DNA topoisomerase II in therapy-related acute promyelocytic leukemia. N Engl J Med (2005) 3.06
The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus. J Exp Med (1998) 2.56
Characterization of a candidate bcl-1 gene. Mol Cell Biol (1991) 2.48
Thermostable DNA polymerase chain amplification of t(14;18) chromosome breakpoints and detection of minimal residual disease. Proc Natl Acad Sci U S A (1988) 2.42
Translation factors promote the formation of two states of the closed-loop mRNP. Nature (2008) 2.31
One-sided polymerase chain reaction: the amplification of cDNA. Proc Natl Acad Sci U S A (1989) 2.25
Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma. Proc Natl Acad Sci U S A (1996) 2.15
Chromosomal translocations cause deregulated BCL6 expression by promoter substitution in B cell lymphoma. EMBO J (1995) 1.94
Follicular lymphomas' BCL-2/IgH junctions contain templated nucleotide insertions: novel insights into the mechanism of t(14;18) translocation. Blood (2000) 1.70
The role of immunoglobulin translocations in the pathogenesis of B-cell malignancies. Blood (2000) 1.66
Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies. Blood (2010) 1.62
The presence of clonogenic cells in high-grade malignant lymphoma: a prognostic factor. Blood (1987) 1.61
Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays. J Med Genet (2003) 1.61
Activation of a translocated c-myc gene: role of structural alterations in the upstream region. Proc Natl Acad Sci U S A (1984) 1.61
Molecular anatomy of BCL6 translocations revealed by long-distance polymerase chain reaction-based assays. Cancer Res (2000) 1.54
The MLL recombinome of acute leukemias. Leukemia (2006) 1.51
Chromatin structure around the c-myc gene in Burkitt lymphomas with upstream and downstream translocation points. Proc Natl Acad Sci U S A (1985) 1.47
Mechanisms of translational deregulation in human tumors and therapeutic intervention strategies. Oncogene (2007) 1.46
High-resolution identification of balanced and complex chromosomal rearrangements by 4C technology. Nat Methods (2009) 1.44
Rapid molecular cloning of rearrangements of the IGHJ locus using long-distance inverse polymerase chain reaction. Blood (1997) 1.41
Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations. Proc Natl Acad Sci U S A (2004) 1.40
A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome. Genome Res (2005) 1.21
Histiocytic lymphoma cell lines: immunologic and cytogenetic studies. Cancer Genet Cytogenet (1985) 1.21
Sequences of human immunoglobulin switch regions: implications for recombination and transcription. Nucleic Acids Res (1990) 1.17
Insertion of excised IgH switch sequences causes overexpression of cyclin D1 in a myeloma tumor cell. Mol Cell (1999) 1.16
Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia. Proc Natl Acad Sci U S A (2002) 1.16
Refinement of lymphoma cytogenetics by the chromosome 18q21 major breakpoint region. Blood (1987) 1.14
Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia. J Mol Diagn (2008) 1.13
Molecular cytogenetic characterization of non-Hodgkin lymphoma cell lines. Genes Chromosomes Cancer (2002) 1.08
Human Ig S gamma regions and their participation in sequential switching to IgE. J Immunol (1995) 1.07
Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers? Blood (2009) 1.06
Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides. Genes Chromosomes Cancer (2003) 1.06
A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis. Mol Cancer (2009) 1.01
Detection of the chromosomal translocation t(11;14) by polymerase chain reaction in mantle cell lymphomas. Blood (1994) 1.01
Molecular characterization of genomic AML1-ETO fusions in childhood leukemia. Leukemia (2001) 0.98
Panhandle polymerase chain reaction amplifies MLL genomic translocation breakpoint involving unknown partner gene. Blood (1997) 0.98
Detection of translocations affecting the BCL6 locus in B cell non-Hodgkin's lymphoma by interphase fluorescence in situ hybridization. Leukemia (2001) 0.98
Pathogenetic and clinical implications of non-immunoglobulin ; BCL6 translocations in B-cell non-Hodgkin's lymphoma. J Clin Exp Hematop (2006) 0.98
Alterations of the p53 tumor suppressor gene in diffuse large cell lymphomas with translocations of the c-MYC and BCL-2 proto-oncogenes. Blood (1994) 0.97
Customized oligonucleotide array-based comparative genomic hybridization as a clinical assay for genomic profiling of chronic lymphocytic leukemia. J Mol Diagn (2008) 0.97
Potential topoisomerase II DNA-binding sites at the breakpoints of a t(9;11) chromosome translocation in acute myeloid leukemia. Cancer Res (1993) 0.93
Molecular diagnosis of mantle cell lymphoma in paraffin-embedded tissue. Mod Pathol (1996) 0.93
Identification of chromosomal translocations in leukemias by hybridization with oligonucleotide microarrays. Haematologica (2002) 0.92
Differences between Burkitt's lymphomas and mouse plasmacytomas in the immunoglobulin heavy chain/c-myc recombinations that occur in their chromosomal translocations. Cancer Res (1995) 0.91
p53 mutations, c-myc and bcl-2 rearrangements in human non-Hodgkin's lymphoma cell lines. Leuk Lymphoma (1995) 0.89
Cloning of the t(11;14)(q13;q32) translocation breakpoints from two human leukemia cell lines. Leukemia (1991) 0.89
Screening and quantification of multiple chromosome translocations in human leukemia. Clin Chem (2003) 0.88
Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t(8;14) translocations in sporadic Burkitt-lymphoma. Leukemia (2007) 0.84
A diagnostic biochip for the comprehensive analysis of MLL translocations in acute leukemia. Leukemia (2004) 0.82
Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genes. Proc Natl Acad Sci U S A (2000) 0.81
Multiple BCL6 translocation partners in individual cases of gastric lymphoma. Blood (2003) 0.79
Deregulation of BCL6 in non-Hodgkin lymphoma by insertion of IGH sequences in complex translocations involving band 3q27. Genes Chromosomes Cancer (1998) 0.77
Translocations into human chromosome 14 JH region: factors influencing downstream abortive immunoglobulin class switching. Mol Immunol (2003) 0.76
Multiple V1/V2 env variants are frequently present during primary infection with human immunodeficiency virus type 1. J Virol (2004) 2.91
Bacterial communities in women with bacterial vaginosis: high resolution phylogenetic analyses reveal relationships of microbiota to clinical criteria. PLoS One (2012) 2.79
Plasma processing conditions substantially influence circulating microRNA biomarker levels. PLoS One (2013) 1.71
Clinical and immunological impact of HIV envelope V3 sequence variation after starting initial triple antiretroviral therapy. AIDS (2004) 1.51
Turnover of env variable region 1 and 2 genotypes in subjects with late-stage human immunodeficiency virus type 1 infection. J Virol (2003) 1.44
Rapid 16S rRNA next-generation sequencing of polymicrobial clinical samples for diagnosis of complex bacterial infections. PLoS One (2013) 1.33
Subtype-specific conformational differences within the V3 region of subtype B and subtype C human immunodeficiency virus type 1 Env proteins. J Virol (2007) 1.14
A format for phylogenetic placements. PLoS One (2012) 1.07
More than meets the eye: associations of vaginal bacteria with gram stain morphotypes using molecular phylogenetic analysis. PLoS One (2013) 1.07
HIV-1 populations in blood and breast milk are similar. Virology (2004) 1.06
IgH partner breakpoint sequences provide evidence that AID initiates t(11;14) and t(8;14) chromosomal breaks in mantle cell and Burkitt lymphomas. Blood (2012) 0.93
Nestly--a framework for running software with nested parameter choices and aggregating results. Bioinformatics (2012) 0.92
Coinfection of Fusobacterium nucleatum and Actinomyces israelii in mastoiditis diagnosed by next-generation DNA sequencing. J Clin Microbiol (2014) 0.84
Compensatory evolution in RNA secondary structures increases substitution rate variation among sites. Mol Biol Evol (2008) 0.81
Early lymph node involvement by mantle cell lymphoma limited to the germinal center: report of a case with a novel "follicular in situ" growth pattern. Am J Clin Pathol (2011) 0.81
Admission oxygenation and ventilation parameters associated with discharge survival in severe pediatric traumatic brain injury. Childs Nerv Syst (2012) 0.80
Hyperglycemia during craniotomy for adult traumatic brain injury. Anesth Analg (2011) 0.79
Molecular diagnosis of Actinomadura madurae infection by 16S rRNA deep sequencing. J Clin Microbiol (2013) 0.78
Case 8-2007: a man with chest pain followed by cardiac arrest. N Engl J Med (2007) 0.75
Design and implementation of software for automated quality control and data analysis for a complex LC/MS/MS assay for urine opiates and metabolites. Clin Chim Acta (2012) 0.75
Vaginal microbiota and genitourinary menopausal symptoms: a cross-sectional analysis. Menopause (2017) 0.75
Simulations of delta check rule performance to detect specimen mislabeling using historical laboratory data. Clin Chim Acta (2011) 0.75