Thomas Eggermann

42PUBLICATIONS
106CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)PharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)Genetic immunologyNutrition and dietetics not elsewhere classified
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Publications (42)

|Jun 25, 2026
Prenatal Genetic Testing for Beckwith-Wiedemann Syndrome: Considerations, Challenges and Observations (A Real-World Study).

|Feb 04, 2026
The potential of whole genome sequencing in pharmacogenetics: a retrospective health record study in rare disease patients.

Madeline Gorny, Katja S Just, Tim Krüger

|Jan 16, 2026
International guideline on genetic testing of children with short stature.

Andrew Dauber, Alexander A L Jorge, Ola Nilsson

|Jan 13, 2026
Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype Correlation.

Anastasia Maria Licata, Elke Botzenhart, Katja Kloth-Stachnau

|Dec 24, 2025
Comprehensive Genetic Testing for Clinical Decision-Making in a Patient With Congenital Hyperinsulinism.

Matthias Begemann, Johannes Alexander Tobias Boy, Florian Kraft

|Nov 10, 2025
Congenital Imprinting Diseases: Aetiology, Pre- and Perinatal Manifestations, Diagnosis and Care of Affected Families and Pregnancies.

Thomas Eggermann, Karl Oliver Kagan, Andreas Dufke

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Frequent Collaborators

8 joint publications

Miriam Elbracht

7 joint publications

Miriam Elbracht

6 joint publications

Florian Kraft

4 joint publications

Ingo Kurth