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Annual Review of Genomics and Human Genetics|May 24, 2015
The Genetics of Soft Connective Tissue DisordersOlivier Vanakker, Bert Callewaert, Fransiska Malfait, et al.
Revista Espanola De Cardiologia (English Ed.)|July 11, 2020
Genetics in congenital heart disease. Are we ready for it?Julie De Backer, Bert Callewaert, Laura Muiño Mosquera
Clinical Genetics|October 15, 2020
Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiologyAude Beyens, Annekatrien Boel, Sofie Symoens, et al.
Advances in Experimental Medicine and Biology|November 22, 2021
Clinical and Molecular Delineation of Cutis Laxa Syndromes: Paradigms for HomeostasisAude Beyens, Lore Pottie, Patrick Sips, et al.
Best Practice & Research. Clinical Rheumatology|March 11, 2008
Ehlers-Danlos syndromes and Marfan syndromeBert Callewaert, Fransiska Malfait, Bart Loeys, et al.
Cornea|March 5, 2025
Ocular Manifestations in Congenital Cutis Laxa: A Case SeriesArnaud Van Slycken, Aude Beyens, Bert Callewaert, et al.
Clinical Genetics|February 18, 2025
Unraveling the Genetic Landscape of Foot Arch Morphology: A Systematic Review of Single Nucleotide PolymorphismsYukun He, Marlies Verleyen, Bert Callewaert, et al.
Ophthalmic Genetics|June 22, 2025
Foveal hypoplasia in Myhre syndrome: a novel associationHelena Van Haecke, Eva Vanbelleghem, Elke O Kreps, et al.
Osteoarthritis and Cartilage|June 9, 2024
A systematic review and cross-database analysis of single nucleotide polymorphisms underlying hip morphology and osteoarthritis reveals shared mechanismsMarlies Verleyen, Yukun He, Arne Burssens, et al.
Genes|April 23, 2022
Expanding the Phenotype of B3GALNT2-Related DisordersErika D'haenens, Sarah Vergult, Björn Menten, et al.
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