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  1. Article

    Open Access

    Pediatric MDS and bone marrow failure-associated germline mutations in SAMD9 and SAMD9L impair multiple pathways in primary hematopoietic cells

    Pediatric myelodysplastic syndromes (MDS) are a heterogeneous disease group associated with impaired hematopoiesis, bone marrow hypocellularity, and frequently have deletions involving chromosome 7 (monosomy 7...

    Melvin E. Thomas III, Sherif Abdelhamed, Ryan Hiltenbrand, Jason R. Schwartz in Leukemia (2021)

  2. Article

    Open Access

    The acquisition of molecular drivers in pediatric therapy-related myeloid neoplasms

    Pediatric therapy-related myeloid neoplasms (tMN) occur in children after exposure to cytotoxic therapy and have a dismal prognosis. The somatic and germline genomic alterations that drive these myeloid neopla...

    Jason R. Schwartz, **g Ma, Jennifer Kamens, Tamara Westover in Nature Communications (2021)

  3. Article

    Open Access

    The genomic landscape of pediatric myelodysplastic syndromes

    Myelodysplastic syndromes (MDS) are uncommon in children and have a poor prognosis. In contrast to adult MDS, little is known about the genomic landscape of pediatric MDS. Here, we describe the somatic and ger...

    Jason R. Schwartz, **g Ma, Tamara Lamprecht, Michael Walsh in Nature Communications (2017)

  4. Article

    Open Access

    Epigenetic alteration by DNA-demethylating treatment restores apoptotic response to glucocorticoids in dexamethasone-resistant human malignant lymphoid cells

    Glucocorticoids (GCs) are often included in the therapy of lymphoid malignancies because they kill several types of malignant lymphoid cells. GCs activate the glucocorticoid receptor (GR), to regulate a comple...

    Aaron L Miller, Chuandong Geng, Georgiy Golovko in Cancer Cell International (2014)