Wouter Steyaert
8PUBLICATIONS
59CO-AUTHORS
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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
|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
|Jun 02, 2021
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
|Feb 01, 2018
Future perspectives of genome-scale sequencing.Wouter Steyaert, Steven Callens, Paul Coucke
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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
