Research Topics
| Ronald J DeLeeuwSummaryAffiliation: British Columbia Country: Canada Publications
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Detail Information
Publications
Whole-genome analysis and HLA genotyping of enteropathy-type T-cell lymphoma reveals 2 distinct lymphoma subtypesRonald J DeLeeuw
Department of Cancer Genetics, British Columbia Cancer Research Centre, Vancouver, British Columbia, Canada
Gastroenterology 132:1902-11. 2007..Enteropathy-type T-cell lymphoma (ETL) is an aggressive extranodal T-cell non-Hodgkin lymphoma assumed to arise in the setting of celiac disease...
Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomesRonald J de Leeuw
Department of Cancer Genetics, British Columbia Cancer Agency, Vancouver, BC, Canada
Hum Mol Genet 13:1827-37. 2004..Further characterization of such minimally altered genomic regions identified using whole genome array CGH will define novel dominant oncogenes and tumor suppressor genes that play important roles in the pathogenesis of MCL...
Sub-megabase resolution tiling (SMRT) array-based comparative genomic hybridization profiling reveals novel gains and losses of chromosomal regions in Hodgkin Lymphoma and Anaplastic Large Cell Lymphoma cell linesFaisal M Fadlelmola
Centre for Translational and Applied Genomics CTAG, Department of Pathology and Laboratory Medicine, British Columbia Cancer Agency, Vancouver Cancer Centre, Vancouver, BC, V5Z 4E6, Canada
Mol Cancer 7:2. 2008....
MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic dataBryan Chi
Department of Cancer Genetics and Developmental Biology, British Columbia Cancer Research Centre, Vancouver, BC, Canada
BMC Bioinformatics 9:243. 2008..Due to the differences in data types it is difficult to conduct parallel analysis of multiple datasets from diverse platforms...
SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization dataBryan Chi
British Columbia Cancer Research Centre, British Columbia Cancer Agency, 601 W, 10th Ave, Vancouver, BC, V5Z 1L3 Canada
BMC Bioinformatics 5:13. 2004..Since array CGH provides signal ratio for each DNA segment, visualization would require the reassembly of individual data points into chromosome profiles...
Cytogenetically balanced translocations are associated with focal copy number alterationsSpencer K Watson
Cancer Genetics and Developmental Biology, British Columbia Cancer Research Centre, 675 West 10th Avenue, Vancouver, BC, Canada
Hum Genet 120:795-805. 2007..Our results reveal that imperfectly balanced translocations in tumor genomes are a phenomenon that occurs at frequencies much higher than previously demonstrated...
A comprehensive analysis of common copy-number variations in the human genomeKendy K Wong
Department of Cancer Genetics and Developmental Biology, University of British Columbia, Vancouver, BC, Canada
Am J Hum Genet 80:91-104. 2007..This in-depth survey of CNVs across the human genome provides a valuable baseline for studies involving human genetics...
A tiling resolution DNA microarray with complete coverage of the human genomeAdrian S Ishkanian
British Columbia Cancer Research Centre, 601 West 10th Avenue, Vancouver, British Columbia V5Z 1L3, Canada
Nat Genet 36:299-303. 2004..Our submegabase resolution tiling set for array CGH (SMRT array) allows comprehensive assessment of genomic integrity and thereby the identification of new genes associated with disease...
Frequent occurrence of deletions in primary mediastinal B-cell lymphomaLindsey R Kimm
Department of Cancer Genetics and Developmental Biology, British Columbia Cancer Research Centre, Vancouver, BC, Canada
Genes Chromosomes Cancer 46:1090-7. 2007..We conclude that consistent losses are present in the PMBCL genome. Given the similar frequency of losses to that of segmental gains of DNA, they are likely to play an important role in the pathogenesis of PMBCL...
NRG1 gene rearrangements in clinical breast cancer: identification of an adjacent novel amplicon associated with poor prognosisLeah M Prentice
Department of Pathology and Prostate Centre, Genetic Pathology Evaluation Centre, Vancouver General Hospital, Vancouver, BC, Canada V6H 3Z6
Oncogene 24:7281-9. 2005..Of the two genes in the novel amplicon, expression of SPFH2 correlated most significantly with amplification. This amplicon may emerge as a result of breakpoints and chromosomal rearrangements within the NRG1 locus...
Identification of novel lung genes in bronchial epithelium by serial analysis of gene expressionKim M Lonergan
Cancer Genetics and Developmental Biology, Department of Cancer Imaging, Canada s Michael Smith Genome Sciences Centre, British Columbia Cancer Research Centre, Vancouver, BC, Canada
Am J Respir Cell Mol Biol 35:651-61. 2006....
Methods for high throughput validation of amplified fragment pools of BAC DNA for constructing high resolution CGH arraysSpencer K Watson
Department of Cancer Genetics and Developmental Biology, BC Cancer Agency, 601 W, 10th Ave, Vancouver, BC, V5Z 1L3 Canada
BMC Genomics 5:6. 2004..The AFP sequencing technique described in this study is a novel method designed to verify the identity of array spotting solution in a high throughput manner...
CD20 mutations involving the rituximab epitope are rare in diffuse large B-cell lymphomas and are not a significant cause of R-CHOP failureNathalie A Johnson
Clinical Professor of Pathology, Department of Pathology, British Columbia Cancer Agency, 600 W 10 Avenue, Vancouver, BC, V5Z 4E6, Canada
Haematologica 94:423-7. 2009..CD20 protein-negative relapses occur after R-CHOP therapy but their clinical relevance is unknown...
