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Search Results to Christopher Wardell

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One or more keywords matched the following items that are connected to Wardell, Christopher

Item TypeName
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 5
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 17
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 14
Concept Chromosome Aberrations
Concept Chromosomes, Human, Pair 16
Concept Physical Chromosome Mapping
Concept Chromosome Breakage
Academic Article Improved risk stratification in myeloma using a microRNA-based classifier.
Academic Article Coexistent hyperdiploidy does not abrogate poor prognosis in myeloma with adverse cytogenetics and may precede IGH translocations.
Academic Article Mapping of chromosome 1p deletions in myeloma identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as being genes in regions associated with adverse survival.
Academic Article Intraclonal heterogeneity and distinct molecular mechanisms characterize the development of t(4;14) and t(11;14) myeloma.
Academic Article Global methylation analysis identifies prognostically important epigenetically inactivated tumor suppressor genes in multiple myeloma.
Academic Article The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy.
Academic Article Gender disparities in the tumor genetics and clinical outcome of multiple myeloma.
Academic Article Characterization of IGH locus breakpoints in multiple myeloma indicates a subset of translocations appear to occur in pregerminal center B cells.
Academic Article A novel functional role for MMSET in RNA processing based on the link between the REIIBP isoform and its interaction with the SMN complex.
Academic Article Identification of a novel t(7;14) translocation in multiple myeloma resulting in overexpression of EGFR.
Academic Article Genomewide profiling of copy-number alteration in monoclonal gammopathy of undetermined significance.
Academic Article Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism.
Academic Article A high-risk, Double-Hit, group of newly diagnosed myeloma identified by genomic analysis.
Academic Article An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome.
Academic Article Structural variants shape the genomic landscape and clinical outcome of multiple myeloma.

Search Criteria
  • Chromosomes Human Pair 1