Esther Schamschula

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Venues

NPJ precision oncology

Human mutation

Epigenetics

Biomolecules

University of Salzburg

Universität Innsbruck (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Salzburg Jun 01 2016 - May 31 2020

Austria

PhD Student :: Biosciences

Education History

Universität Innsbruck Jul 23 2012 - Apr 08 2015

Austria

MSC :: Molecular Cell- and Developmental Biology

Universität Innsbruck Jul 14 2009 - Jul 23 2012

Austria

BSC :: Biology

Publications

Richard Gallon, Carlijn Brekelmans, Marie Martin, Vincent Bours, Esther Schamschula, Albert Amberger, Martine Muleris, Chrystelle Colas, Jeroen Dekervel, Gert De Hertogh, Jérôme Coupier, Orphal Colleye, Edith Sepulchre, John Burn, Hilde Brems, Eric Legius, Katharina Wimmer
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants. NPJ precision oncology 8 (1) (2024)
Richard Gallon, Carlijn Brekelmans, Marie Martin, Vincent Bours, Esther Schamschula, Albert Amberger, Martine Muleris, Chrystelle Colas, Jeroen Dekervel, Gert De Hertogh, Jérôme Coupier, Orphal Colleye, Edith Sepulchre, John Burn, Hilde Brems, Eric Legius, Katharina Wimmer
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants. NPJ precision oncology 8 (1) (2024)
Esther Schamschula, Miriam Kinzel, Annekatrin Wernstedt, Klaus Oberhuber, Hendrik Gottschling, Simon Schnaiter, Nicolaus Friedrichs, Sabine Merkelbach-Bruse, Johannes Zschocke, Richard Gallon, Katharina Wimmer
Teenage-Onset Colorectal Cancers in a Digenic Cancer Predisposition Syndrome Provide Clues for the Interaction between Mismatch Repair and Polymerase δ Proofreading Deficiency in Tumorigenesis. Biomolecules 12 (10) (2022)
Esther Schamschula, Angelika Lahnsteiner, Yassen Assenov, Wolfgang Hagmann, Nadja Zaborsky, Markus Wiederstein, Anna Strobl, Frauke Stanke, Thomas Muley, Christoph Plass, Burkhard Tümmler, Angela Risch
Disease-related blood-based differential methylation in cystic fibrosis and its representation in lung cancer revealed a regulatory locus in PKP3 in lung epithelial cells. Epigenetics (2021)
Katharina Wimmer, Esther Schamschula, Annekatrin Wernstedt, Pia Traunfellner, Albert Amberger, Johannes Zschocke, Peter Kroisel, Yunjia Chen, Tom Callens, Ludwine M Messiaen
AG-exclusion zone revisited: Lessons to learn from 91 intronic NF1 3' splice site mutations outside the canonical AG-dinucleotides. Human mutation 41 (6) (2020)

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Publication Activity (10 Years)

Top Topics

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Esther Schamschula