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Gregor Hoermann

23PUBLICATIONS

60CO-AUTHORS

Haematological tumoursDevelopmental genetics (incl. sex determination)Molecular targetsCell and nuclear divisionMedical biotechnology diagnostics (incl. biosensors)

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Publications (23)

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|May 05, 2026

Complex Karyotype in CLL-How to Count Cytogenetic Aberrations Consistently and Efficiently.

|Apr 14, 2026

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

Sandra Huber, Christoph Kornauth, Stephan Hutter

|Mar 19, 2026

Multiple myeloma with concomitant chronic lymphocytic leukemia: evidence for independent clonal origin.

Jana Wobst, Henning Ruge, Sara Senk

|May 19, 2025

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

Sandra Huber, Stephan Hutter, Constance Baer

|Dec 20, 2024

Correspondence response to: can patient ancestry influence molecular classifications in myeloid neoplasms?

Gregor Hoermann, Yuri Fedoriw, Joseph D Khoury

|Dec 17, 2024

Somatic Recombination Between an Ancient and a Recent <i>NOTCH2</i> Gene Variant Is Associated with the NOTCH2 Gain-of-Function Phenotype in Chronic Lymphocytic Leukemia.

Rainer Hubmann, Martin Hilgarth, Tamara Löwenstern

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Frequent Collaborators

8 joint publications

Wolfgang Kern

7 joint publications

Torsten Haferlach

6 joint publications

Claudia Haferlach

6 joint publications

Peter Valent

5 joint publications

Manja Meggendorfer

5 joint publications

Constance Baer

5 joint publications

Georg Greiner

4 joint publications

Stephan Hutter

3 joint publications

Gregor Eisenwort

3 joint publications

Sandra Huber

Frequent Collaborators

8 joint publications

Wolfgang Kern

7 joint publications

Torsten Haferlach

6 joint publications

Claudia Haferlach

6 joint publications

Peter Valent

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