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November 24, 2025BloodOpen Access

Whole genome transcriptome sequencing in inherited bone marrow failure syndromes and related diseases – the ibmdx study

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Authors

WSWilliam G. StevensonGLGraham J. LieschkeNENicole den Elzen

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Cite This Study

Stevenson et al. (2025) studied this question.

synapsesocial.com/papers/69403d892d562116f290d415https://doi.org/10.1182/blood-2025-lba-4
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Genomic insights into inherited bone marrow failure syndromes in a Korean population2024 · 4 citations
  2. 2A prospective Study of whole genome sequencing for genomic profiling and risk determination in MDS2025
  3. 3Abstract 5300: Clinical utility of whole genome sequencing for upfront risk stratification in AML and MDS patients2026
  4. 4Clinical Profile of Adults with Inherited Bone Marrow Failure Syndromes: Results of an Ambispective Clinical Single-Center Study2024
  5. 5Rapid hematologic germline testing using hair follicle-derived DNA for germline predisposition and inherited marrow failure states2025