Maxim Verlee

4PUBLICATIONS

22CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsCardiology (incl. cardiovascular diseases)

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Publications (4)

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|Jul 01, 2026

Evaluation of the Diagnostic Yield of Exome-Based Panels for Congenital Heart Defects in Different Clinical Settings.

|Apr 01, 2025

Correction: RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease.

Maxim Verlee, Erika D'haenens, Laurenz De Cock

|Jan 27, 2025

RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease.

Maxim Verlee, Erika D'haenens, Laurenz De Cock

|Apr 03, 2021

Loss-of-Function Variants in <i>EFEMP1</i> Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations.

Maxim Verlee, Aude Beyens, Alper Gezdirici

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Frequent Collaborators

4 joint publications

Bert Callewaert

3 joint publications

Laura Muiño Mosquera

2 joint publications

Kristof Vandekerckhove

Tim Van Damme

Sarah Vergult

Aude Beyens

Alper Gezdirici

Elif Yilmaz Gulec

Silke De Feyter

Michiel Vanhooydonck

Frequent Collaborators

4 joint publications

Bert Callewaert

3 joint publications

Laura Muiño Mosquera

2 joint publications

Kristof Vandekerckhove

2 joint publications

Tim Van Damme