Researcher
Ilse Meerschaut
- Keywords (Vrije Universiteit Brussel):Medicine
- Keywords (Ghent University):Clinical genetics, Pediatric cardiology, Congenital heart defects, Pediatrics, Medical genetics
- Disciplines (Ghent University):Genetics, Molecular diagnostics, Paediatrics, Cardiology
- See also: Ilse Meerschaut (Vrije Universiteit Brussel)
Affiliations
- Pediatrics (Department)
Member
From1 Jan 2023 → Today - Pediatrics (Department)
Member
From1 Sep 2022 → 31 Dec 2022 - Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 25 Sep 2022 - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2015 → 30 Sep 2018
Publications
1 - 10 of 17
- The effect of statins on vascular function in adolescents with familial hypercholesterolemia : a literature review(2024)
Authors: Astrid De Wolf, Willem Staels, Ilse Meerschaut, Daniël De Wolf, Jesse Vanbesien, Elise Nauwynck, Inge Gies, Jean De Schepper
Pages: 81 - 88 - Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects(2022)
Authors: Gerarda Cappuccio, Nicola BrunettiU+2010Pierri, Paul Clift, Christopher Learn, John C. Dykes, Catherine L. Mercer, Bert Callewaert, Ilse Meerschaut, Alessandro Mauro Spinelli, Irene Bruno, et al.
Pages: 1384 - 1395 - Exploring the mutational landscape of isolated congenital heart defects : an exome sequencing study using cardiac DNA(2022)
Authors: Ilse Meerschaut, Wouter Steyaert, Thierry Bové, Katrien Francois, Thomas Martens, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, et al.
- Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases(2022)
Authors: Nancy Vegas, Zeynep Demir, Christopher T. Gordon, Sylvain Breton, Vanessa L. Romanelli Tavares, Hugo Moisset, Roseli ZechiU+2010Ceide, Nancy M. KokitsuU+2010Nakata, Yasuhiro Kido, Sandrine Marlin, et al.
Pages: 582 - 594 - A reassessment of copy number variations in congenital heart defects : picturing the whole genome(2021)
Authors: Ilse Meerschaut, Sarah Vergult, Annelies Dheedene, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Daniël De Wolf, Bert Callewaert
- Expanding the phenotypic and molecular landscape of syndromic and isolated congenital heart defects : a future for phenotype-first and genotype-first approaches(2021)
Authors: Ilse Meerschaut
- A clinical scoring system for congenital contractural arachnodactyly(2020)
Authors: Ilse Meerschaut, Wouter Steyaert, Angela Barnicoat, Allan Bayat, Francesco Benedicenti, Siren Berland, Edward M. Blair, Jeroen Breckpot, Anna de Burca, Anne Destrée, et al.
Pages: 124 - 131 - Two novel probands with Myhre syndrome identified through WES(2019)Volume: 27
Authors: Ilse Meerschaut, Aude Beyens, Wouter Steyaert, Riet De Rycke, Björn Menten, Katrien Bonte, Tine De Backer, Sandra Janssens, Fransiska Malfait, Joseph Panzer, et al.
Pages: 118 - 118 - Myhre syndrome : a first familial recurrence and broadening of the phenotypic spectrum(2019)
Authors: Ilse Meerschaut, Aude Beyens, Wouter Steyaert, Riet De Rycke, Katrien Bonte, Tine De Backer, Sandra Janssens, Joseph Panzer, Frank Plasschaert, Daniël De Wolf, et al.
Pages: 2494 - 2499 - Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline(2018)
Authors: Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Wouter Steyaert, Bert Callewaert, Marjolijn Renard