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Wouter Steyaert

8PUBLICATIONS

59CO-AUTHORS

Gene mappingEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Rehabilitation engineering

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Publications (8)

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|Mar 26, 2025

Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencing.

Wouter Steyaert, Lydia Sagath, German Demidov

|May 15, 2024

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.

Wouter Steyaert, Lydia Sagath, German Demidov

|Nov 17, 2023

Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.

Robin Wijngaard, German Demidov, Luke O'Gorman

|Oct 18, 2023

Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.

Robin Wijngaard, German Demidov, Luke O'Gorman

|Jul 27, 2022

Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA.

Ilse Meerschaut, Wouter Steyaert, Thierry Bové

|Jul 16, 2021

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.

Elke de Boer, Charlotte W Ockeloen, Leslie Matalonga

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Frequent Collaborators

6 joint publications

Christian Gilissen

6 joint publications

Lisenka E L M Vissers

4 joint publications

Volker Straub

3 joint publications

Rita Horvath

3 joint publications

Steven Laurie

3 joint publications

Luke O'Gorman

3 joint publications

German Demidov

2 joint publications

Charlotte W Ockeloen

2 joint publications

Aurélien Trimouille

2 joint publications

Alain Verloes

Frequent Collaborators

6 joint publications

Christian Gilissen

6 joint publications

Lisenka E L M Vissers

4 joint publications

Volker Straub

3 joint publications

Rita Horvath

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