Low Rate of Germline Investigation for Variants of Suspected Germline Origin Detected During the Diagnostic Work‐Up of Myeloid Neoplasms
We report a low investigation rate for variants of suspected germline origin detected during the genomic profiling of patients investigated for MN in the clinical setting. Our study underscores the need for further awareness regarding germline investigation for hematological malignancies. <b>Trial Registration</b>: The authors have confirmed clinical trial registration is not needed for this submission.
Authors
- Arielle R. Munters (ORCID: https://orcid.org/0000-0003-1512-6565)
- Rose‐Marie Amini (ORCID: https://orcid.org/0000-0003-0901-5252)
- Panagiotis Baliakas (ORCID: https://orcid.org/0000-0002-5634-7156)
- Thale Kristin Olsen (ORCID: https://orcid.org/0000-0003-4655-7384)
- Jörg Cammenga (ORCID: https://orcid.org/0000-0001-5573-7542)
- Tatjana Pandzic (ORCID: https://orcid.org/0009-0006-9032-4616)
- Claes Ladenvall (ORCID: https://orcid.org/0000-0002-7501-6598)
- Ahmed Al‐Djaber (ORCID: https://orcid.org/0000-0001-7352-2852)
Institutions
- Uppsala University (SE)
- Lund University (SE)
- Science for Life Laboratory (SE)
- Skåne University Hospital (SE)
Publication Details
- Journal
- eJHaem
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1002/jha2.70206
- Primary Topic
- Acute Myeloid Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Swedish Cancer Foundation
- Cancerfonden
- Barncancerfonden
- Uppsala Universitet
- Svenska Läkaresällskapet
- Science for Life Laboratory