Dominik Sebastian Westphal

19PUBLICATIONS
137CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthNeurogeneticsCardiology (incl. cardiovascular diseases)Molecular medicine
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Publications (19)

|Mar 19, 2026
Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results.

Korbinian M Riedhammer, Patrick Richthammer, Dominik S Westphal

|Jul 02, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohort.

Lea Lippert, Tobias Burkard, Franziska Markel

|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

|Apr 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy.

Nadine Spielmann, Gregor Miller, Tudor I Oprea

|Dec 23, 2024
Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail Syndrome.

Alina Kurolap, Chofit Chai Gadot, Orly Eshach Adiv

|Dec 09, 2024
Eccentric hypertrophy impairs outcome after TAVR.

R Thalmann, V Obermeier, Dominik S Westphal

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Frequent Collaborators

6 joint publications

Matias Wagner

4 joint publications

Cordula Wolf

4 joint publications

Korbinian M Riedhammer

3 joint publications

Theresa Brunet