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Wan L. Lam

Researcher at BC Cancer Research Centre

Publications -  313
Citations -  22171

Wan L. Lam is an academic researcher from BC Cancer Research Centre. The author has contributed to research in topics: Cancer & Comparative genomic hybridization. The author has an hindex of 72, co-authored 297 publications receiving 20104 citations. Previous affiliations of Wan L. Lam include Dalhousie University & BC Cancer Agency.

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Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells.

TL;DR: Analysis of 6,000 CpG islands showed that only a small set of promoters was methylated differentially, suggesting that aberrant methylation of CpGs island promoters in malignancy might be less frequent than previously hypothesized.
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The functional role of long non-coding RNA in human carcinomas

TL;DR: The emerging functional role of lncRNAs in human cancer is highlighted and molecular mechanisms by which these RNA species function are described, providing insight into the functional roles they may play in tumorigenesis.
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A tiling resolution DNA microarray with complete coverage of the human genome.

TL;DR: The constructed tiling resolution array allows comprehensive assessment of genomic integrity and thereby the identification of new genes associated with disease and shows the need to move beyond conventional marker-based genome comparison approaches, that rely on inference of continuity between interval markers.
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Identification of miR-145 and miR-146a as mediators of the 5q– syndrome phenotype

TL;DR: Deletes chromosome 5q and identifies Toll–interleukin-1 receptor domain–containing adaptor protein (TIRAP) and tumor necrosis factor receptor–associated factor-6 (TRAF6) as respective targets of these miRNAs.
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A Comprehensive Analysis of Common Copy-Number Variations in the Human Genome

TL;DR: An in-depth survey of CNVs across the human genome provides a valuable baseline for studies involving human genetics and raises the possibility of the contribution of microRNAs to phenotypic diversity in humans.