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Alex-Vincent Postma

6PUBLICATIONS

85CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsAutonomic nervous systemComputational physiologyDevelopmental genetics (incl. sex determination)

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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

Frequent Collaborators

3 joint publications

Vincent M Christoffels

2 joint publications

Rafik Tadros

2 joint publications

Arjan C Houweling

2 joint publications

Seema Mital

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