Jarl Bastianen About Jarl Bastianen Jarl Bastianen Contact Campus Drie Eiken Show email address Tel. +3232759745 Prins Boudewijnlaan 43 2650 Edegem, BEL Department Genetics, Pharmacology and Physiopathology of Heart, Blood Vessels and Skeleton Cookie prreferences Strictly necessary cookies They are …

Jarl Bastianen Publications Jarl Bastianen Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype Source Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15 Author(s) Hanne Boen, Maaike Alaerts, Lut Van Laer, Johan Saenen, Inge Goovaerts, …

Jarl Bastianen Over Jarl Bastianen Jarl Bastianen Contact Campus Drie Eiken Toon e-mailadres Tel. +3232759745 Prins Boudewijnlaan 43 2650 Edegem, BEL Afdeling Genetica, Farmacologie en Fysiopathologie van Hart, Bloedvaten en Skelet Cookie-voorkeuren Strikt noodzakelijke cookies Ze zijn noodzakelijk …

Jarl Bastianen Publicaties Jarl Bastianen Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype Bron Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15 Auteur(s) Hanne Boen, Maaike Alaerts, Lut Van Laer, Johan Saenen, Inge Goovaerts, Jar…

Aline Verstraeten associate research professor Publications Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Source Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Author…

Aline Verstraeten hoofddocent Publicaties Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Auteur(s) Joe Davis Velche…

Lut Van Laer associate professor Publications Lut Van Laer Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14…

Maaike Bastiaansen Publications Maaike Bastiaansen Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome Source Npj genomic medicine - ISSN 2056-7944-9:1 (2024) p. 1-9 Author(s) Josephina Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathry…

Josephina Meester assistant professor - postdoc researcher FWO Publications Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine -…

Josephina Meester docent - postdoc mandaat FWO Publicaties Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:…

Lut Van Laer hoofddocent Publicaties Lut Van Laer Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14 Auteur(s) …

Maaike Bastiaansen Publicaties Maaike Bastiaansen Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome Bron Npj genomic medicine - ISSN 2056-7944-9:1 (2024) p. 1-9 Auteur(s) Josephina Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathryn A…

Genomics in Medicine - GENOMED search menu search content Members GENOMED Research teams Cardiovascular Genetics (MEDGEN) PI: Prof. Dr. Bart Loeys & Prof. Dr. Lut Van Laer Postdocs: Dr. Aline Verstraeten, Dr. Maaike Alaerts & Dr. Dorien Schepers PhD students: Josephina Meester, Ajay Kumar, Elyssa Ca…

Lucia Buccioli predoc researcher FWO Publications Lucia Buccioli Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Source International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Author(s) Ir…

Mandy Vermont spec. staff member - expert Publications Mandy Vermont A human importin-β-related disorder : syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8 Source The American journal of human genetics - ISSN 0002-9297-108:6 (2021) p. 1115-1125 Author(s) Ils…

Irene Valdivia Callejon predoc researcher FWO Publications Irene Valdivia Callejon Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Source International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p.…

Lucia Buccioli predoc mandaat FWO Publicaties Lucia Buccioli Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Auteur(s) Irene Va…

Irene Valdivia Callejon predoc mandaat FWO Publicaties Irene Valdivia Callejon Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 …

Mandy Vermont gespecialiseerd med.- expert Publicaties Mandy Vermont A human importin-β-related disorder : syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8 Bron The American journal of human genetics - ISSN 0002-9297-108:6 (2021) p. 1115-1125 Auteur(s) Ilse …

Silke Peeters unpaid staff Publications Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Source Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Author(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, Bart Loeys …

Silke Peeters onbezoldigd medewerker Publicaties Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Bron Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Auteur(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, Bart…

Ilse Luyckx senior researcher Publications Ilse Luyckx Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals Source Journal of medical genetics - ISSN 0022-2593-62:3 (2025) p. 199-205 Author(s) Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A. Boswell-Patterson, Ingrid M.B.H…

Laura Rabaut Publications Laura Rabaut An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Source Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Author(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, …

Jolien Schippers Publications Jolien Schippers An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Source Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Author(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van …

Laura Rabaut Publicaties Laura Rabaut An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Bron Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Auteur(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, Tyc…