Alex-Vincent Postma
6PUBLICATIONS
85CO-AUTHORS
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Publications (6)
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|Jan 08, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects.Gregor Dombrowsky, Liselot van der Laan, Ananília Silva
|Jun 06, 2025
A novel heterozygous pathogenic variant in HEY2 led to a familial form of non-syndromic Tetralogy of Fallot.Camille Bergès, Fanny Laffargue, Claire Dauphin
|May 17, 2023
Genetics of sinoatrial node function and heart rate disorders.Lieve E van der Maarel, Alex V Postma, Vincent M Christoffels
|Feb 03, 2022
Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.Antoinette F van Ouwerkerk, Fernanda M Bosada, Karel van Duijvenboden
|Dec 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.Doris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada
|Mar 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.Najim Lahrouchi, Aman George, Ilham Ratbi
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Frequent Collaborators
3 joint publications
Vincent M Christoffels
2 joint publications
Rafik Tadros
2 joint publications
Arjan C Houweling
2 joint publications
Seema Mital
2 joint publications
Jeroen Breckpot
2 joint publications
Elisabeth M Lodder
2 joint publications
Sven Dittrich
2 joint publications
David Winlaw
2 joint publications
Connie R Bezzina
2 joint publications
Felix Berger
