Ivanna Fedoryshchenko predoc mandaat FWO Publicaties Ivanna Fedoryshchenko Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation Bron Stem cell research - ISSN 1873-5061-69 (2023) p. 1-5 Auteur(s) Ilse Van Gucht, Lu…

Lisa Van Linden predoc researcher FWO Research Lisa Van Linden Research team Functional Morphology Poor but prosperous: how island biota survive genetic impoverishment. 01/11/2022 - 31/10/2026 Abstract Although often genetically impoverished due to founder effects, inbreeding, genetic drift, and seq…

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…

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 …

Ivanna Fedoryshchenko predoc researcher FWO Publications Ivanna Fedoryshchenko Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation Source Stem cell research - ISSN 1873-5061-69 (2023) p. 1-5 Author(s) Ilse Van Guc…

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…

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, …

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…

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…

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 Research Irene Valdivia Callejon Research team Medical Genetics (MEDGEN) Investigating thoracic aortic aneurysm pathogenesis at single-cell resolution. 01/11/2022 - 31/10/2026 Abstract Thoracic aortic aneurysm (TAA) is an abnormal widening of the aorta i…

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, …

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…

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…

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, …

Benny Borremans unpaid staff Research Benny Borremans Research team Evolutionary ecology group (EVECO) Quantifying the transmission dynamics of two rodentborne viral infections in a variable environment. 01/10/2013 - 30/09/2015 Abstract For a better understanding of the transmission of infections, a…

μNEURO search menu search content Translational Neurosciences Recent publications Antigen-specific treatment modalities in MS : the past, the present, and the future Source Frontiers in immunology - ISSN 1664-3224-12 (2021) p. Author(s) Judith Derdelinckx, Patrick Cras, Zwi Nisan Berneman, Nathalie…

Ayşe Candayan Niron postdoc researcher FWO Research Ayşe Candayan Niron Research team VIB CMN - Molecular Neurogenomics Expertise I am a human geneticist specialized in neuromuscular diseases. I have broad experience in second- and third-generation sequencing analyses, cellular and molecular biolo…

Arvid Suls research manager Research Arvid Suls Research team Medical Genetics (MEDGEN) Expertise Currently, I am the research manager of the Genomics in Medicine (GENOMED) consortium. I'm a molecular geneticist with more than 10 years expertise in next-generation sequencing, bio-informatics and gen…

Antwerp Surgical Training, Anatomy and Research Centre search menu search content Molecular genetics - current research Molecular genetic detection of susceptibility to malignant hyperthermia in Belgian families L Heytens Responsible Research Group Maligne Hyperthermia University of Antwerp C Van Br…

Ilse Luyckx senior researcher Research Ilse Luyckx Research team Medical Genetics (MEDGEN) Expertise Projects: • Unravelling the pathological key events underlying SMAD6-deficiency in patients with bicuspid aortic valve-related aortopathy • Unravelling the genetic architecture of (bicuspid aorti…

Antwerp Surgical Training, Anatomy and Research Centre search menu search content Malignant hyperthermia Malignant hyperthermia. ‘Malignanthyperthermia’ (MH) is a life-threatening, potentially fatal complication ofgeneral anesthesia triggered by the commonly used inhalational anesthesics andsucc…