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Genomic landscape and chronological reconstruction of driver events in multiple myeloma

https://doi.org/10.1101/388611
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1 of 34 checkable references need attention · checked 2026-07-23

At the dated check, the references listed below either did not resolve in Crossref or DataCite, or carried a retraction notice. Each one is shown with the registry record that put it there.

References needing attention

does not resolve to a known work10.1038/leu.2017.344
The 33 checked references that resolve
resolves10.1182/blood-2014-10-567370
Genetics of multiple myeloma: another heterogeneity level?
resolves10.1038/nrclinonc.2016.122
Genomic complexity of multiple myeloma and its clinical implications
resolves10.1038/nrc3257
The genetic architecture of multiple myeloma
resolves10.1038/ncomms7997
APOBEC family mutational signatures are associated with poor prognosis translocations in multiple myeloma
resolves10.1038/ncomms3997
Heterogeneity of genomic evolution and mutational profiles in multiple myeloma
resolves10.1038/nature09837
Initial genome sequencing and analysis of multiple myeloma
resolves10.1016/j.ccr.2013.12.015
Widespread Genetic Heterogeneity in Multiple Myeloma: Implications for Targeted Therapy
resolves10.1200/JCO.2014.59.1503
Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma
resolves10.1182/blood-2012-01-405985
Clonal competition with alternating dominance in multiple myeloma
resolves10.1038/leu.2012.226
Minor clone provides a reservoir for relapse in multiple myeloma
resolves10.1038/leu.2013.199
Intraclonal heterogeneity is a critical early event in the development of myeloma and precedes the development of clinical symptoms
resolves10.1038/leu.2017.345
Biological and prognostic impact of APOBEC-induced mutations in the spectrum of plasma cell dyscrasias and multiple myeloma cell lines
resolves10.1038/bcj.2017.94
High somatic mutation and neoantigen burden are correlated with decreased progression-free survival in multiple myeloma
resolves10.1126/science.aab4082
Somatic mutation in cancer and normal cells
resolves10.1126/science.aaa6806
High burden and pervasive positive selection of somatic mutations in normal human skin
resolves10.1182/blood-2016-07-729954
Recurrent somatic mutations affecting B-cell receptor signaling pathway genes in follicular lymphoma
resolves10.1016/j.celrep.2018.01.088
Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types
resolves10.1038/nature14666
Non-coding recurrent mutations in chronic lymphocytic leukaemia
resolves10.1016/j.cell.2017.09.027
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
resolves10.1038/s41375-018-0103-3
Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms
resolves10.1101/181339
Patterns of structural variation in human cancer
resolves10.1016/j.cell.2013.02.023
Criteria for Inference of Chromothripsis in Cancer Genomes
resolves10.1038/nature13115
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
resolves10.1016/j.cell.2015.11.054
Chromothripsis and Kataegis Induced by Telomere Crisis
resolves10.1182/blood-2011-03-344069
Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients
resolves10.1001/jamaoncol.2015.2010
Treatment With Carfilzomib-Lenalidomide-Dexamethasone With Lenalidomide Extension in Patients With Smoldering or Newly Diagnosed Multiple Myeloma
resolves10.1038/leu.2014.70
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma
resolves10.1002/gcc.20123
Characterization of oncogene dysregulation in multiple myeloma by combined FISH and DNA microarray analyses
resolves10.1038/bcj.2017.12
Bi-allelic inactivation is more prevalent at relapse in multiple myeloma, identifying RB1 as an independent prognostic marker
resolves10.1101/161562
The evolutionary history of 2,658 cancers
resolves10.1038/s41467-017-00296-y
Spatial genomic heterogeneity in multiple myeloma revealed by multi-region sequencing
resolves10.1016/j.cell.2012.04.023
The Life History of 21 Breast Cancers
resolves10.1182/blood-2012-12-471888
Characterization of IGH locus breakpoints in multiple myeloma indicates a subset of translocations appear to occur in pregerminal center B cells
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

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