Katharina Wimmer

16PUBLICATIONS
43CO-AUTHORS
Gene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Social epidemiologyHaematological tumoursPredictive and prognostic markers
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Publications (16)

|Aug 27, 2026
The Tyrolean Founder MLH1 Variant c.836T>G Causes Lynch Syndrome Due to a Leaky Splice Effect.

|Jun 09, 2026
Hereditary cancer: Germline testing practices across ERN GENTURIS member countries.

|Mar 03, 2026
Reporting practices for secondary findings among ERN GENTURIS member institutions in 15 European countries.

Kathrin Taxer, Katharina Wimmer, Karin Wadt

|Oct 17, 2024
ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management.

Chrystelle Colas, Léa Guerrini-Rousseau, Manon Suerink

|Jun 19, 2024
Stratification of Homologous Recombination Deficiency-Negative High-Grade Ovarian Cancer by the Type of Peritoneal Spread into Two Groups with Distinct Survival Outcomes.

Simon Schnaiter, Esther Schamschula, Juliane Laschtowiczka

|May 24, 2024
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.

Richard Gallon, Carlijn Brekelmans, Marie Martin

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Frequent Collaborators

4 joint publications

Richard Gallon

4 joint publications

Esther Schamschula

3 joint publications

Johannes Zschocke

3 joint publications

Simon Schnaiter