Onderzoeker
Ilse Meerschaut
- Trefwoorden (Vrije Universiteit Brussel):Geneeskunde
- Trefwoorden (Ghent University):Kindergeneeskunde, Klinische genetica, Aangeboren hartafwijkingen, Medische genetica, Kindercardiologie
- Disciplines (Ghent University):Genetica, Moleculaire diagnostiek, Pediatrie, Cardiologie
- Zie ook: Ilse Meerschaut (Vrije Universiteit Brussel)
Affiliaties
- Pediatrie (Departement)
Lid
Vanaf1 jan 2023 → Heden - Pediatrie (kind) (Departement)
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Vanaf1 sep 2022 → 31 dec 2022 - Vakgroep Biomoleculaire Geneeskunde (Departement)
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Vanaf1 okt 2018 → 25 sep 2022 - Vakgroep Pediatrie en genetica (Departement)
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Vanaf1 okt 2015 → 30 sep 2018
Publicaties
1 - 10 van 17
- The effect of statins on vascular function in adolescents with familial hypercholesterolemia : a literature review(2024)
Auteurs: Astrid De Wolf, Willem Staels, Ilse Meerschaut, Daniël De Wolf, Jesse Vanbesien, Elise Nauwynck, Inge Gies, Jean De Schepper
Pagina's: 81 - 88 - Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects(2022)
Auteurs: 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.
Pagina's: 1384 - 1395 - Exploring the mutational landscape of isolated congenital heart defects : an exome sequencing study using cardiac DNA(2022)
Auteurs: 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)
Auteurs: 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.
Pagina's: 582 - 594 - A reassessment of copy number variations in congenital heart defects : picturing the whole genome(2021)
Auteurs: 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)
Auteurs: Ilse Meerschaut
- A clinical scoring system for congenital contractural arachnodactyly(2020)
Auteurs: Ilse Meerschaut, Wouter Steyaert, Angela Barnicoat, Allan Bayat, Francesco Benedicenti, Siren Berland, Edward M. Blair, Jeroen Breckpot, Anna de Burca, Anne Destrée, et al.
Pagina's: 124 - 131 - Two novel probands with Myhre syndrome identified through WES(2019)Volume: 27
Auteurs: Ilse Meerschaut, Aude Beyens, Wouter Steyaert, Riet De Rycke, Björn Menten, Katrien Bonte, Tine De Backer, Sandra Janssens, Fransiska Malfait, Joseph Panzer, et al.
Pagina's: 118 - 118 - Myhre syndrome : a first familial recurrence and broadening of the phenotypic spectrum(2019)
Auteurs: 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.
Pagina's: 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)
Auteurs: Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Wouter Steyaert, Bert Callewaert, Marjolijn Renard