Publications by authors named "Sabrina Haslinger"

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Identification of a novel amplified PAX5::RBPMS fusion gene in pediatric B-cell acute lymphoblastic leukemia.
Sabrina Haslinger, Dagmar Schinnerl, Margit König, Andrea Inthal, Klaus Fortschegger

Leuk Res· July 2025

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PAX5::AUTS2 childhood B-ALL: a relapse-prone genetic subtype with frequent central nervous system involvement and a poor outcome.
Aurélie Caye-Eude, Grazia Fazio, Agata Pastorczak, Judith M Boer, Doris Steinemann, Sabrina Haslinger

Leukemia· February 2025

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Body-wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.
Eva-Maria Dauber, Oskar A Haas, Karin Nebral, Christoph Gassner, Sabrina Haslinger

Br J Haematol· September 2024

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Risk factors in DUX4-positive childhood and adolescent B-cell acute lymphoblastic leukemia.
Dagmar Schinnerl, Marion Riebler, Angela Schumich, Sabrina Haslinger, Alice Bramböck

Blood Cancer J· July 2024

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Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia.
M Reza Abbasi, Karin Nebral, Sabrina Haslinger, Andrea Inthal, Petra Zeitlhofer

Cancers (Basel)· September 2021

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CD371 cell surface expression: a unique feature of -rearranged acute lymphoblastic leukemia.
Dagmar Schinnerl, Ester Mejstrikova, Angela Schumich, Marketa Zaliova, Klaus Fortschegger, Sabrina Haslinger

Haematologica· August 2019

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Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3).
Theodora Malli, Melanie Rammer, Sabrina Haslinger, Jonathan Burghofer, Sonja Burgstaller

Mol Cytogenet· January 2018

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