Spectrum of abnormalities and clonal transformation in germline RUNX1 familial platelet disorder and a genomic comparative analysis with somatic RUNX1 mutations in MDS/MPN overlap neoplasms

Emma C. DiFilippo, Giacomo Coltro, Ryan M. Carr, Abhishek A. Mangaonkar, Moritz Binder, Shakila P. Khan, Vilmarie Rodriguez, Naseema Gangat, Alexandra Wolanskyj, Rajiv K. Pruthi, Dong Chen, Rong He, David S. Viswanatha, Terra Lasho, Christy Finke, Ayalew Tefferi, Animesh Pardanani, Mrinal M. Patnaik

Research output: Contribution to journalLetter

Original languageEnglish (US)
JournalLeukemia
DOIs
StateAccepted/In press - 2020

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

Cite this

DiFilippo, E. C., Coltro, G., Carr, R. M., Mangaonkar, A. A., Binder, M., Khan, S. P., Rodriguez, V., Gangat, N., Wolanskyj, A., Pruthi, R. K., Chen, D., He, R., Viswanatha, D. S., Lasho, T., Finke, C., Tefferi, A., Pardanani, A., & Patnaik, M. M. (Accepted/In press). Spectrum of abnormalities and clonal transformation in germline RUNX1 familial platelet disorder and a genomic comparative analysis with somatic RUNX1 mutations in MDS/MPN overlap neoplasms. Leukemia. https://doi.org/10.1038/s41375-020-0752-x