Ilse Meerschaut

9PUBLICATIONS
110CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Respiratory 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.

|Sep 10, 2024
Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens

|Jul 12, 2024
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens

|Mar 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.

Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara

|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

|Jan 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects.

Gerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift

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Frequent Collaborators

8 joint publications

Bert Callewaert

3 joint publications

Julie De Backer

3 joint publications

Laura Muiño Mosquera

2 joint publications

Kathleen Claes