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Human Molecular Genetics|March 28, 2024
Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relationNathalie P de Wagenaar, Lisa M van den Bersselaar, Hanny J H M Odijk, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|March 19, 2025
Pregnancy and Delivery Outcomes in Vascular Ehlers-Danlos Syndrome: A Retrospective Multicentre Cohort StudyLisa M van den Bersselaar, Ingrid M B H van de Laar, Marieke J H Baars, et al.
JCI Insight|August 10, 2023
Biallelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organizationClaudine Wb Ruijmbeek, Filomena Housley, Hafiza Idrees, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2022
Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohortLisa M van den Bersselaar, Judith M A Verhagen, Jos A Bekkers, et al.
Circulation. Genomic and Precision Medicine|April 16, 2024
Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 PatientsSerwet Demirdas, Lisa M van den Bersselaar, Rosan Lechner, et al.
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