Gerarda Van De Beek
Antwerpen, VLG 2650, Belgium
Last Updated: 09/26/2026
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Found 9 publications
varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data.
Journal: Bioinformatics (Oxford, England)
Published: February 13, 2022
Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool.
Journal: Frontiers in medicine
Published: May 22, 2019
Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in EFEMP2.
Journal: Molecular syndromology
Published: February 15, 2018
Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype.
Journal: Journal of medical genetics
Published: February 02, 2018
Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.
Journal: Frontiers in physiology
Published: August 09, 2017
Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.
Journal: Frontiers in physiology
Published: April 14, 2017
TGF-β signalopathies as a paradigm for translational medicine.
Journal: European journal of medical genetics
Published: July 06, 2015
Application of full field optical studies for pulsatile flow in a carotid artery phantom.
Journal: Biomedical optics express
Published: May 13, 2015
Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.
Journal: Journal of the American College of Cardiology
Published: October 06, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026