Claus-Eric Ott

10PUBLICATIONS
195CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)
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Publications (10)

|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann

|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann

|Jun 17, 2024
A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric mass.

Stefan Habringer, Jana Ihlow, Karsten Kleo

|Mar 13, 2024
Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study.

Alisa Maria Vittoria Reiter, Jean Tori Pantel, Magdalena Danyel

|Oct 06, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.

Christopher Hakkaart, John F Pearson, Louise Marquart

|Jul 27, 2022
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.

Martine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant

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Frequent Collaborators

5 joint publications

Jean Tori Pantel

4 joint publications

Malte Spielmann

3 joint publications

Martin Atta Mensah

3 joint publications

Peter M Krawitz