Elke Holinski-Feder

10PUBLICATIONS
37CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsOptical technologyCell and nuclear divisionLiquid biopsies
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Publications (10)

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

|Mar 11, 2026
Validation structures for sequence variants of uncertain significance in hereditary cancer.

Morghan C Lucas, Thomas Keßler, Anna Benet-Pagès

|Oct 29, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic Strategies.

Lukas Neuhann, Andreas Laner, Elke Holinski-Feder

|May 03, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?

Morghan C Lucas, Thomas Keßler, Florentine Scharf

|Dec 20, 2024
Updated Structure of CNBP Repeat Expansions in Patients With Myotonic Dystrophy Type 2 and Its Implication for Standard Diagnostics.

Martin Wendlandt, Hannes Erdmann, Simone Rost

|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

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Frequent Collaborators

5 joint publications

Verena Steinke-Lange

3 joint publications

Barbara Klink

3 joint publications

Thomas Keßler

3 joint publications

Morghan C Lucas