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Blood Cancer Journal|January 25, 2020
The significance of genetic mutations and their prognostic impact on patients with incidental finding of isolated del(20q) in bone marrow without morphologic evidence of a myeloid neoplasmAishwarya Ravindran, Rong He, Rhett P Ketterling, et al.
Human Pathology|April 13, 2026
Next-Generation Sequencing for Lymphoid Neoplasms: Real-World Utility from a Clinical AssayChuan Chen, Cody J Artymiuk, Tanya L Schwab, et al.
American Journal of Clinical Pathology|December 14, 2020
Novel t(1;8)(p31.3;q21.3) NFIA-RUNX1T1 Translocation in an Infant Erythroblastic SarcomaRebecca L King, Parwiz J Siaghani, Katy Wong, et al.
American Journal of Clinical Pathology|June 23, 2016
Lymphoplasmacytic Lymphoma With a Non-IgM Paraprotein Shows Clinical and Pathologic Heterogeneity and May Harbor MYD88 L265P MutationsRebecca L King, Wilson I Gonsalves, Stephen M Ansell, et al.
Nature Genetics|May 27, 2014
Recurrent PAX3-MAML3 fusion in biphenotypic sinonasal sarcomaXiaoke Wang, Krista L Bledsoe, Rondell P Graham, et al.
British Journal of Haematology|September 17, 2013
Patients with chronic lymphocytic leukaemia and clonal deletion of both 17p13.1 and 11q22.3 have a very poor prognosisPatricia T Greipp, Stephanie A Smoley, David S Viswanatha, et al.
Platelets|April 29, 2016
Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a familyJuliana Perez Botero, Dong Chen, Rong He, et al.
American Journal of Hematology|May 24, 2018
Genotype-Phenotype Correlation of Hereditary Erythrocytosis Mutations, a single center experienceJennifer L Oliveira, Lea M Coon, Lori A Frederick, et al.
Genes, Chromosomes & Cancer|October 20, 2020
Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemiaHolly E Berg, Patrick R Blackburn, Linda B Baughn, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 1, 2019
Hybridization capture-based next generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysisRong He, Daniel J Devine, Zheng Jin Tu, et al.
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