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        - 2024
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                        Mark
        Osteosarcomas With Few Chromosomal Alterations or Adult Onset Are Genetically Heterogeneous
    
    - Contribution to journal › Article
 
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                        Mark
        MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma
    
    - Contribution to journal › Article
 
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                        Mark
        Transcriptomic profiles of myxofibrosarcoma and undifferentiated pleomorphic sarcoma correlate with clinical and genomic features
    
    - Contribution to journal › Article
 
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                        Mark
        Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway
    
    - Contribution to journal › Article
 
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                        Mark
        CDK4 is co-amplified with either TP53 promoter gene fusions or MDM2 through distinct mechanisms in osteosarcoma
    
    - Contribution to journal › Article
 
- 2023
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                        Mark
        Insertion of the CXXC domain of KMT2A into YAP1 : An unusual mechanism behind the formation of a chimeric oncogenic protein
    
    - Contribution to journal › Article
 
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                        Mark
        Inactivation of RB1, CDKN2A and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells
    
    - Contribution to journal › Article
 
- 2022
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                        Mark
        Overlapping morphological, immunohistochemical and genetic features of superficial CD34-positive fibroblastic tumor and PRDM10-rearranged soft tissue tumor
    
    - Contribution to journal › Article
 
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                        Mark
        Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma : A potential treatment target in rare cases?
    
    - Contribution to journal › Article
 
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                        Mark
        The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
    
    - Contribution to journal › Article
 
