- ORCID iD
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0000-0002-9078-1415
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Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease
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Evaluation of the diagnostic yield of exome-based panels for congenital heart defects in different clinical settings
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Septal coronary artery fistula after implantation of a left bundle branch area pacemaker
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RNA-sequencing unveils novel FLT4 splice site variants in isolated CHD
(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.691-691 -
- Journal Article
- A1
- open access
Shprintzen-Goldberg syndrome : follow-up of the cardiovascular features in an international cohort of 29 patients with SGS
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- Journal Article
- A2
- open access
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease
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- Journal Article
- A1
- open access
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease
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Early mechanisms of aortic failure in a zebrafish model for thoracic aortic dissection and rupture
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Early mechanisms of aortic failure in a zebrafish model for thoracic aortic dissection and rupture
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The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture