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Tommy Martinsson

Sahlgrenska University Hospital

29

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2022

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Influence of segmental chromosome abnormalities on survival in children over the age of 12 months with unresectable localised peripheral neuroblastic tumours without MYCN amplification.

2015 British Journal of Cancer
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Aggressive neuroblastomas have high p110alpha but low p110delta and p55alpha/p50alpha protein levels compared to low stage neuroblastomas

2013 Journal of Molecular Signaling
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Identification of epigenetically regulated genes that predict patient outcome in neuroblastoma

2011 BMC Cancer
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MYCN amplicon junctions as tumor-specific targets for minimal residual disease detection in neuroblastoma

2011 International Journal of Oncology
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Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors

2011 BMC Genomics
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Characterization of amplicon junction sequences in genomic regions surrounding the MYCN gene in neuroblastoma tumors; implications for clinical follow-up of high-risk patients in FEBS JOURNAL, vol 278, issue , pp 215-215

2011
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High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset

2010 Proceedings of the National Academy of Sciences of the United States of America
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The Phox2 pathway is differentially expressed in neuroblastoma tumors, but no mutations were found in the candidate tumor suppressor gene PHOX2A.

2009 International Journal of Oncology
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High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: Four cases of homozygous deletions of the CDKN2A gene

2008 BMC Genomics
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The two human homologues of yeast UFD2 ubiquitination factor, UBE4A and UBE4B, are located in common neuroblastoma deletion regions and are subject to mutations in tumours

2006 European Journal of Cancer
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Citations (23)