Single-molecule analysis reveals widespread structural variation in multiple myeloma

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The current status of minimal residual disease assessment in myeloma

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Heterogeneity of genomic evolution and mutational profiles in multiple myeloma

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Characterization of IGH locus breakpoints in multiple myeloma indicates a subset of translocations appear to occur in pregerminal center B cells

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Discovery of structural alterations in solid tumor oligodendroglioma by single molecule analysis

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The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

(2013) Niels Weinhold et al.   NATURE GENETICS

Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

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Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides

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(2011) S. Vincent Rajkumar   AMERICAN JOURNAL OF HEMATOLOGY

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CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

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Initial genome sequencing and analysis of multiple myeloma

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Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

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Genome structural variation discovery and genotyping

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Multiple Myeloma

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A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value

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Bone marrow stromal cells from multiple myeloma patients uniquely induce bortezomib resistant NF-κB activity in myeloma cells

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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

(2010) Francesca Antonacci et al.   NATURE GENETICS

High-resolution human genome structure by single-molecule analysis

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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

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The role of the insulin-like growth factor 1 receptor axis in multiple myeloma

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Deletions of CDKN2C in Multiple Myeloma: Biological and Clinical Implications

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