Last Updated: 09/26/2026
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Found 56 publications
Timing is everything: age-dependent cancer risk in RUNX1-FPD.
Journal: Blood advances
Published: May 01, 2026
Protocol optimization improves the performance of multiplexed RNA imaging.
Journal: Scientific reports
Published: March 21, 2025
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.
Journal: Blood advances
Published: February 23, 2023
Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham).
Journal: Pediatric blood & cancer
Published: July 12, 2022
Opening the window for endothelial-to-hematopoietic transition.
Journal: Genes & development
Published: November 02, 2021
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy.
Journal: Haematologica
Published: March 22, 2021
B-cell acute lymphoblastic leukemia in patients with germline RUNX1 mutations.
Journal: Blood advances
Published: March 05, 2021
Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript.
Journal: The Journal of experimental medicine
Published: February 22, 2021
CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: September 05, 2020
Last Updated: 09/26/2026