Sandra Huber

7PUBLICATIONS

23CO-AUTHORS

Medical mycologyHaematological tumoursDevelopmental genetics (incl. sex determination)Immunogenetics (incl. genetic immunology)Cell and nuclear division

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Publications (7)

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|Jul 13, 2026

Subclonal MECOM rearrangements in myeloid neoplasms: enriched for TP53 mutations and adverse outcome.

|May 09, 2026

The clinical relevance of sole loss of chromosome Y in myeloid neoplasms.

|Apr 14, 2026

Genetic characterization of AML defined by differentiation shows a high frequency of DDX41 mutations.

Sandra Huber, Christoph Kornauth, Stephan Hutter

|Mar 20, 2026

IDH1- and IDH2-mutated myeloid neoplasms: mutational pattern, clonal hierarchy, and the role in AML transformation.

Sandra Huber, Flora Goessweiner, Wencke Walter

|May 19, 2025

Two ways to complex karyotype in MDS-the role of del(5q) and TP53.

Sandra Huber, Stephan Hutter, Constance Baer

|May 07, 2025

Myelodysplastic neoplasms with ring sideroblasts without SF3B1 mutations in adults: enrichment of germline variants in congenital sideroblastic anemia genes.

Sandra Novoa-Jáuregui, Sandra Huber, Maria Gabarrós-Subirà

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Frequent Collaborators

Torsten Haferlach

Stephan Hutter

Gregor Hoermann

Wolfgang Kern

Claudia Haferlach

Manja Meggendorfer

Isolde Summerer

Maria Gabarrós-Subirà

1 joint publications

Anna Stengel

1 joint publications

Salvador Carrillo-Tornel

Frequent Collaborators

Torsten Haferlach

Stephan Hutter

Gregor Hoermann

Wolfgang Kern