Karin Nebral
Vienna, Austria
Last Updated: 09/26/2026
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Found 39 publications
Pitfalls and Challenges in the Detection of ZNF384 Rearrangements by Fluorescence in Situ Hybridization.
Journal: Genes, chromosomes & cancer
Published: May 03, 2026
Biological and clinical characteristics of ETV6::RUNX1-like ALL.
Journal: HemaSphere
Published: August 28, 2025
Epigenetic remodeling via HDAC6 inhibition amplifies anti-tumoral immune responses in myeloid leukemia cells.
Journal: Cell death & disease
Published: August 03, 2025
Duplication in the HLA-B/-C region on the short arm of chromosome 6.
Journal: Vox sanguinis
Published: May 22, 2025
PAX5::AUTS2 childhood B-ALL: a relapse-prone genetic subtype with frequent central nervous system involvement and a poor outcome.
Journal: Leukemia
Published: October 18, 2024
Erratum to: Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard risk acute myeloid leukemia.
Journal: Haematologica
Published: July 01, 2024
Risk factors in DUX4-positive childhood and adolescent B-cell acute lymphoblastic leukemia.
Journal: Blood cancer journal
Published: May 07, 2024
Body-wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.
Journal: British journal of haematology
Published: April 24, 2024
Transcriptional and epigenetic rewiring by the NUP98::KDM5A fusion oncoprotein directly activates CDK12.
Journal: Nature communications
Published: March 06, 2024
A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.
Journal: HemaSphere
Published: August 02, 2023
Last Updated: 09/26/2026