Ariane Hallermayr

8PUBLICATIONS
12CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Liquid biopsiesPredictive and prognostic markersNeurogenetics
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Publications (8)

|Oct 23, 2026
Decoding common and complex genotypes of facioscapulohumeral muscular dystrophy using methylation profiling and long-read sequencing.

|Jun 05, 2024
The utility of liquid biopsy in clinical genetic diagnosis of cancer and monogenic mosaic disorders.

Ariane Hallermayr, Thomas Keßler, Verena Steinke-Lange

|Oct 28, 2023
Impact of cfDNA Reference Materials on Clinical Performance of Liquid Biopsy NGS Assays.

Ariane Hallermayr, Thomas Keßler, Moritz Fujera

|Feb 15, 2022
Clinical Validity of Circulating Tumor DNA as Prognostic and Predictive Marker for Personalized Colorectal Cancer Patient Management.

Ariane Hallermayr, Verena Steinke-Lange, Holger Vogelsang

|Aug 15, 2021
Liquid Biopsy Hotspot Variant Assays: Analytical Validation for Application in Residual Disease Detection and Treatment Monitoring.

Ariane Hallermayr, Anna Benet-Pagès, Verena Steinke-Lange

|Nov 21, 2018
Extending the critical regions for mutations in the non-coding gene RNU4ATAC in another patient with Roifman Syndrome.

Ariane Hallermayr, Janine Graf, Udo Koehler

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Frequent Collaborators

3 joint publications

Verena Steinke-Lange

2 joint publications

Hannes Erdmann

2 joint publications

Benedikt Schoser

2 joint publications

Elke Holinski-Feder