Eva Froňková

9PUBLICATIONS
60CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsHaematological tumoursMedical infection agents (incl. prions)Medical mycologyCancer genetics
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Publications (9)

|Oct 27, 2025
Atypical Phenotype of Predominant Autoimmune Cytopenia and Impaired Perforin Expression in XMEN Syndrome.

Hana Grombirikova, Adam Markocsy, Anna Kocurkova

|Mar 25, 2025
Overt and covert genetic causes of pediatric acute lymphoblastic leukemia.

Ulrik Stoltze, Stefanie V Junk, Anna Byrjalsen

|Sep 13, 2024
Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion.

Marketa Rackova, Rafael Mattera, Michael Svaton

|May 14, 2024
Analysis of measurable residual disease by IG/TR gene rearrangements: quality assurance and updated EuroMRD guidelines.

Vincent H J van der Velden, Isabel Dombrink, Julia Alten

|Mar 08, 2024
Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease.

Martin Schwarz, Matej Gazdarica, Eva Froňková

|Oct 14, 2022
NGS better discriminates true MRD positivity for the risk stratification of childhood ALL treated on an MRD-based protocol.

Michael Svaton, Aneta Skotnicova, Leona Reznickova

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Frequent Collaborators

4 joint publications

Jan Trka

4 joint publications

Michael Svaton

3 joint publications

Michaela Kotrova

2 joint publications

Vincent H J van der Velden