Last Updated: 09/26/2026
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Found 34 publications
Consolidation Therapy Based on Mutation Clearance in Acute Myeloid Leukemia.
Journal: NEJM evidence
Published: August 25, 2026
Exome sequencing of Hodgkin and non-Hodgkin composite lymphomas identifies shared somatic mutations indicative of common founding precursors.
Journal: Cancer genetics
Published: September 09, 2025
Combined Kdm6a and Trp53 Deficiency Drives the Development of Squamous Cell Skin Cancer in Mice.
Journal: The Journal of investigative dermatology
Published: April 13, 2022
Distinct clonal identities of B-ALLs arising after lenolidomide therapy for multiple myeloma.
Journal: Blood advances
Published: March 07, 2022
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 25, 2021
Kdm6a deficiency restricted to mouse hematopoietic cells causes an age- and sex-dependent myelodysplastic syndrome-like phenotype.
Journal: PloS one
Published: July 15, 2021
Tumor suppressor function of WT1 in acute promyelocytic leukemia.
Journal: Haematologica
Published: July 09, 2021
Tumor suppressor function of Gata2 in acute promyelocytic leukemia.
Journal: Blood
Published: March 18, 2021
Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia.
Journal: JCO precision oncology
Published: October 16, 2020
Shared cell of origin in a patient with Erdheim-Chester disease and acute myeloid leukemia.
Journal: Haematologica
Published: March 30, 2019
Fifty Shades of GATA2 Mutation: A Case of Plasmablastic Lymphoma, Nontuberculous Mycobacterial Infection, and Myelodysplastic Syndrome.
Journal: Clinical lymphoma, myeloma & leukemia
Published: March 04, 2019
Last Updated: 09/26/2026