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- 2021
- BL1391 : an established cell line from a human malignant peripheral nerve sheath tumor with unique genomic features
- “Inflammatory Leiomyosarcoma” and “Histiocyte-rich Rhabdomyoblastic Tumor” : a clinicopathological, immunohistochemical and genetic study of 13 cases, with a proposal for reclassification as “Inflammatory Rhabdomyoblastic Tumor”
- 2020
- Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
- PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
- Deep sequencing of myxoinflammatory fibroblastic sarcoma
- Genomic and transcriptomic features of dermatofibrosarcoma protuberans : Unusual chromosomal origin of the COL1A1-PDGFB fusion gene and synergistic effects of amplified regions in tumor development
- 2019
- Aberrant receptor tyrosine kinase signaling in lipofibromatosis : a clinicopathological and molecular genetic study of 20 cases
- Cancer chromosome breakpoints cluster in gene-rich genomic regions
- Most gene fusions in cancer are stochastic events
- Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile