16 resultaten gevonden
Publications Aline Verstraeten | Aline Verstraeten | University of Antwerp
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…
Publications Ilse Luyckx | Ilse Luyckx | University of Antwerp
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…
Publications Laura Rabaut | Laura Rabaut | University of Antwerp
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, …
Publicaties Laura Rabaut | Laura Rabaut | Universiteit Antwerpen
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…
Publicaties Aline Verstraeten | Aline Verstraeten | Universiteit Antwerpen
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…
Publicaties Ilse Luyckx | Ilse Luyckx | Universiteit Antwerpen
Ilse Luyckx senior onderzoeker Publicaties Ilse Luyckx Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals Bron Journal of medical genetics - ISSN 0022-2593-62:3 (2025) p. 199-205 Auteur(s) Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A. Boswell-Patterson, Ingrid M.B.H. …
Publications Lut Van Laer | Lut Van Laer | University of Antwerp
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…
Publications Maaike Bastiaansen | Maaike Bastiaansen | University of Antwerp
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…
Publications Anne Hebert | Anne Hebert | University of Antwerp
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…
Publications Jarl Bastianen | Jarl Bastianen | University of Antwerp
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, …
Publications Josephina Meester | Josephina Meester | University of Antwerp
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 -…
Publicaties Josephina Meester | Josephina Meester | Universiteit Antwerpen
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:…
Publicaties Anne Hebert | Anne Hebert | Universiteit Antwerpen
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, …
Publicaties Jarl Bastianen | Jarl Bastianen | Universiteit Antwerpen
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…
Publicaties Lut Van Laer | Lut Van Laer | Universiteit Antwerpen
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) …
Publicaties Maaike Bastiaansen | Maaike Bastiaansen | Universiteit Antwerpen
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…