Maaike Bastiaansen About Maaike Bastiaansen Maaike Bastiaansen Contact Campus Drie Eiken Show email address Prins Boudewijnlaan 43 2650 Edegem, BEL Department Genetics, Pharmacology and Physiopathology of Heart, Blood Vessels and Skeleton Cookie prreferences Strictly necessary cookies They are neces…

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…

Maaike Bastiaansen Over Maaike Bastiaansen Maaike Bastiaansen Contact Campus Drie Eiken Toon e-mailadres Prins Boudewijnlaan 43 2650 Edegem, BEL Afdeling Genetica, Farmacologie en Fysiopathologie van Hart, Bloedvaten en Skelet Cookie-voorkeuren Strikt noodzakelijke cookies Ze zijn noodzakelijk voor …

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…

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 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…

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…

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 …

Sara Nullens unpaid guest prof. Publications Sara Nullens Belgian consensus on the management of patients with functional dyspepsia Source Acta gastro-enterologica belgica - ISSN 1784-3227-88:2 (2025) p. 157-178 Author(s) S. Kindt, J. Arts, P. Caenepeel, F. de Clerck, Heiko de Schepper, H. Louis, P.…

Sara Nullens onbezoldigd gastprofessor Publicaties Sara Nullens Belgian consensus on the management of patients with functional dyspepsia Bron Acta gastro-enterologica belgica - ISSN 1784-3227-88:2 (2025) p. 157-178 Auteur(s) S. Kindt, J. Arts, P. Caenepeel, F. de Clerck, Heiko de Schepper, H. Louis…

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…

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, …

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…

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…

Lotte Van Den Heuvel unpaid staff Publications Lotte Van Den Heuvel 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. Couck…

Anne Hebert predoc researcher FWO Publications Anne Hebert Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies Source Genome medicine - ISSN 1756-994X-17:1 (2025) p. 1-16 Author(s) Francesca Mattioli, Rún Friðriksdóttir, Anne Hebert, Sissy Bassani, Nazia Ibr…

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:…

Lotte Van Den Heuvel onbezoldigd medewerker Publicaties Lotte Van Den Heuvel 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…

Anne Hebert predoc mandaat FWO Publicaties Anne Hebert Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies Bron Genome medicine - ISSN 1756-994X-17:1 (2025) p. 1-16 Auteur(s) Francesca Mattioli, Rún Friðriksdóttir, Anne Hebert, Sissy Bassani, Nazia Ibrahim, …

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) …

GENCOR Dogan Akdeniz function researcher Show email address Maaike Alaerts function assistant professor - senior researcher tel: 032759700 tel: +3232759780 Show email address Reihaneh Asadi function doctoral scholarship holder Show email address Maaike Bastiaansen function Show email address Jarl Ba…

GENCOR Dogan Akdeniz functie onderzoeker Toon e-mailadres Maaike Alaerts functie docent - senior onderzoeker tel: 032759700 tel: +3232759780 Toon e-mailadres Reihaneh Asadi functie doctoraatsbursaal Toon e-mailadres Maaike Bastiaansen functie Toon e-mailadres Jarl Bastianen functie tel: +3232759745 …

Fac Medicine & Health Sciences Fien Aben function predoc researcher FWO Show email address Andrea Abou Yaghi function doctoral scholarship holder Show email address Daniel Abramowicz function emeritus occasional assignment tel: +3238213970 Show email address Pascale Abrams function unpaid staff tel:…