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Researcher
Maxim Verlee
Profile
Projects
Publications
Activities
Awards & Distinctions
6
Results
2025
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease
Maxim Verlee
Erika D'haenens
Laurenz De Cock
Laura Muiño Mosquera
Katya De Groote
Kristof Vandekerckhove
Joseph Panzer
Ellen Roets
Björn Menten
Sofie Symoens
et al.
U
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2025
2024
Early mechanisms of aortic failure in a zebrafish model for thoracic aortic dissection and rupture
Michiel Vanhooydonck
Maxim Verlee
Marta Guerreiro Santana Ramos Da Silva
Lore Pottie
Annekatrien Boel
Matthias Van Impe
Hanna De Saffel
Lisa Caboor
Piyanoot Tapaneeyaphan
Anne Bonnin
et al.
Preprint
2024
Early mechanisms of aortic failure in a zebrafish model for thoracic aortic dissection and rupture
Michiel Vanhooydonck
Maxim Verlee
Marta Guerreiro Santana Ramos Da Silva
Lore Pottie
Annekatrien Boel
Matthias Van Impe
Hanna De Saffel
Lisa Caboor
Piyanoot Tapaneeyaphan
Anne Bonnin
et al.
U
Conference
2024
2023
The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture
Michiel Vanhooydonck
Maxim Verlee
Lore Pottie
Annekatrien Boel
Piyanoot Tapaneeyaphan
Marta Guerreiro Santana Ramos Da Silva
Adelbert De Clercq
Lisa Caboor
Matthias Van Impe
Delfien Syx
et al.
C3
Conference
2023
The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture
Michiel Vanhooydonck
Maxim Verlee
Lore Pottie
Annekatrien Boel
Piyanoot Tapaneeyaphan
Marta Guerreiro Santana Ramos Da Silva
Adelbert De Clercq
Lisa Caboor
Matthias Van Impe
Delfien Syx
et al.
C3
Conference
2023
2021
Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations
Maxim Verlee
Aude Beyens
Alper Gezdirici
Elif Gulec
Lore Pottie
Silke De Feyter
Michiel Vanhooydonck
Piyanoot Tapaneeyaphan
Sofie Symoens
Bert Callewaert
A1
Journal Article
in
GENES
2021