Wilhelmina S Kerstjens-Frederikse

9PUBLICATIONS
121CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)MechanobiologyDevelopmental genetics (incl. sex determination)Cardiology (incl. cardiovascular diseases)
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Publications (9)

|Jul 01, 2026
Evaluation of the Diagnostic Yield of Exome-Based Panels for Congenital Heart Defects in Different Clinical Settings.

|Mar 19, 2026
Navigating the use of preimplantation genetic testing: a retrospective analysis of 15 years of the Dutch National Indications Committee for PGT.

Rio N Kramers, Vyne van der Schoot, Eva H Brilstra

|Sep 06, 2023
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return.

Emily A Huth, Xiaonan Zhao, Nichole Owen

|Jul 19, 2022
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease.

Matina Prapa, Mauro Lago-Docampo, Emilia M Swietlik

|Dec 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Doris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada

|Aug 30, 2021
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility.

Aafke Engwerda, Erika K S M Leenders, Barbara Frentz

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Frequent Collaborators

2 joint publications

Aafke Engwerda

2 joint publications

Rafik Tadros

2 joint publications

Conny M A van Ravenswaaij-Arts

2 joint publications

Marc Gewillig