Richard Press
Affiliations: | Oregon Health and Science University, Portland, OR |
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Werstein B, Dunlap J, Cascio MJ, et al. (2019) Molecular discordance between myeloid sarcomas and concurrent bone marrows occurs in actionable genes and is associated with worse overall survival. The Journal of Molecular Diagnostics : Jmd |
Dunlap JB, Leonard J, Rosenberg M, et al. (2019) The combination of NPM1, DNMT3A and IDH1/2 mutations leads to inferior overall survival in AML. American Journal of Hematology |
Werstein B, Dunlap J, Cascio M, et al. (2018) 325 Myeloid Sarcomas and Concurrent Bone Marrow Biopsies May Demonstrate Discordant Mutational Profiles by Massively Parallel Sequencing American Journal of Clinical Pathology. 149: S140-S140 |
Ma J, Dunlap J, Paliga A, et al. (2017) DNMT3A co-mutation is required for FLT3-ITD as an adverse prognostic indicator in intermediate-risk cytogenetic group AML. Leukemia & Lymphoma. 1-11 |
Raess PW, Cascio MJ, Fan G, et al. (2016) Concurrent STAT3, DNMT3A and TET2 mutations in T-LGL leukemia with molecularly distinct clonal hematopoiesis of indeterminate potential. American Journal of Hematology |
Wiedmeier JE, Kato C, Zhang Z, et al. (2016) Clonal hematopoiesis as determined by the HUMARA assay is a marker for acquired mutations in epigenetic regulators in older women. Experimental Hematology |
Reinig E, Yang F, Traer E, et al. (2016) Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia. American Journal of Clinical Pathology |
Shi M, Spurgeon S, Press R, et al. (2015) MYD88 mutation analysis of a rare composite chronic lymphocyte leukemia and lymphoplasmacytic lymphoma by flow cytometry cell sorting. Annals of Hematology. 94: 1941-4 |
Ang D, Fan G, Traer E, et al. (2013) Utility of Multiplex Mutation Analysis in the Diagnosis of Chronic Myelomonocytic Leukemia Journal of Leukemia. 1: 1-6 |
Dunlap J, Beadling C, Warrick A, et al. (2012) Multiplex high-throughput gene mutation analysis in acute myeloid leukemia. Human Pathology. 43: 2167-76 |