Clinical, genetic, and familial features of <i>POT1</i> tumor predisposition syndrome
This analysis provides insights into the clinical features and familial patterns of malignancy of individuals with POT1-TPD. Identification through genetic counseling and augmented cancer screening is paramount.
Authors
- Matteo Molica (ORCID: https://orcid.org/0000-0001-6391-4406)
- Prithviraj Bose (ORCID: https://orcid.org/0000-0002-4343-5712)
- Alessandra Ferrajoli (ORCID: https://orcid.org/0000-0001-9547-4193)
- Jennifer Croden (ORCID: https://orcid.org/0000-0002-2634-4341)
- Alexandre Bazinet (ORCID: https://orcid.org/0000-0001-5538-4943)
- Abhishek Maiti (ORCID: https://orcid.org/0000-0001-9043-538X)
- F. Haddad
- Nitin Jain
- Hagop Kantarjian
- Courtney D. DiNardo
- Jan Burger
- William Wierda
- Hiam M. Abdel‐Salam
- Tapan Kadia
Institutions
- The University of Texas MD Anderson Cancer Center (US)
- Cancer Genetics (United States) (US)
Publication Details
- Journal
- Cancer
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1002/cncr.70315
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00