Onderzoeker
Griet Van Buggenhout
- Disciplines:Genetica, Systeembiologie, Medische beeldvorming en therapie, Moleculaire en celbiologie, Andere paramedische wetenschappen
Affiliaties
- Departement Menselijke Erfelijkheid (Departement)
Lid
Vanaf1 dec 2000 → Heden
Publicaties
11 - 20 van 36
- Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome(2020)
Auteurs: Gilles Droogmans, Ann Swillen, Griet Van Buggenhout
Pagina's: 1 - 12 - Adolescent met schizofreniformestoornis en terugkerende 16p11.2-duplicatie [Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication](2019)
Auteurs: Jean Steyaert, Hilde Peeters, Griet Van Buggenhout
Pagina's: 421 - 425 - Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing(2018)
Auteurs: Nathalie Brison, Maria Neofytou, Baran Bayindir, Kris Van Den Bogaert, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel de l'Argentière, Koenraad Devriendt
Pagina's: 258 - 266 - Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator(2017)
Auteurs: Nele Cosemans, Jeroen Breckpot, Thomy de Ravel de l'Argentière, Griet Van Buggenhout, Hilde Peeters, Prosper Lukusa-Tshilobo, Koenraad Devriendt
Pagina's: 166 - 171 - Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies(2017)
Auteurs: Nathalie Brison, Kris Van Den Bogaert, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel de l'Argentière, Eric Legius, Koenraad Devriendt, Joris Vermeesch
Pagina's: 306 - 313 - Whole-gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development(2017)
Auteurs: Griet Van Buggenhout
Pagina's: 106 - 110 - Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies(2017)
Auteurs: Nathalie Brison, Kris Van Den Bogaert, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel de l'Argentière, Eric Legius, Koenraad Devriendt, Joris Vermeesch
Pagina's: 469 - 470 - Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor(2016)
Auteurs: Jeroen Breckpot, Griet Van Buggenhout, Nathalie Brison, Joris Vermeesch, Marina Danckaerts, Pascal Sienaert, Koenraad Devriendt, Annick Vogels
Pagina's: 436 - 443 - THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability(2015)
Auteurs: Griet Van Buggenhout, Hilde Van Esch
Pagina's: 302 - 10 - Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder(2014)
Auteurs: Griet Van Buggenhout
Pagina's: 459 - 467