Researcher
Ann Swillen
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Behaviour and Neurodevelopment (Division)
Responsible
From1 Oct 2019 → Today - Department of Human Genetics (Department)
Member
From1 Jan 2012 → Today - Research Group for Adapted Physical Activity and Psychomotor Rehabilitation (Division)
Member
From1 Oct 2005 → 31 Dec 2011 - Department of Rehabilitation Sciences (Department)
Member
From1 Oct 2002 → 30 Sep 2005
Projects
1 - 5 of 5
- Deep familial phenotyping and genotyping to resolve phenotypic variability of inherited pathogenic genetic variantsFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- Segmental duplication structural variation as the cause for the 22q11DS phenotypic variabilityFrom1 Jan 2017 → 31 Dec 2020Funding: FWO research project (including WEAVE projects)
- Breakpoint variability as an explanation for phenotypical variation in 22q11DS.From1 Aug 2013 → 11 Jun 2020Funding: IWT personal funding - strategic basic research grants
- Pragmatic language skills in children with 22q11.2 deletion syndrome and Williams syndromeFrom1 Oct 2012 → 31 Jan 2017Funding: Private funding of national origin - undefined
- Resequencing remaining allele in atypical 22q11 deletion carriers to identify genetic modifiers of the velo-cardio-facial syndrome (VCFS).From1 Jun 2009 → 31 May 2011Funding: Foreign foundations, funds with scientific view
Publications
91 - 100 of 119
- Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes(2013)
Authors: Ann Swillen, Joris Vermeesch, Koenraad Devriendt, Maude Schneider
Pages: 439 - 447 - Adaptieve vaardigheden, cognitief functioneren en gedragsproblemen bij adolescenten met het 22q11.2-deletiesyndroom [Adaptive skills, cognitive functioning and behavioural problems in adolescents with 22q11.2 deletion syndrome](2013)
Authors: Ilse Noens, Ann Swillen
Pages: 369 - 74 - Wat met genetica?(2013)
Authors: Jan Aerts, Pascal Borry, Ronny Decorte, Koenraad Devriendt, Kris Dierickx, Gert Matthijs, Yves Moreau, Erik Schokkaert, Ann Swillen, Hilde Van Esch, et al.
Number of pages: 120 - Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients(2012)
Authors: Sean B Herman, Tingwei Guo, Donna M McDonald McGinn, Anna Blonska, Alan L Shanske, Anne S Bassett, Eva WC Chow, Mark Bowser, Molly Sheridan, Frits Beemer, et al.
Pages: 2781 - 2787 - Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients(2012)
Authors: Koenraad Devriendt, Ann Swillen, Jeroen Breckpot
Pages: 2781 - 2787 - Social phenotypes in genetic syndromes(2012)
Authors: Ann Swillen, Thomy de Ravel de l'Argentière
Pages: 919 - 921 - Neuropsychopathology in 7 patients with the 22q13 deletion syndrome: presence of bipolar disorder and progressive loss of skills(2012)
Authors: Hilde Van Esch, Thomy de Ravel de l'Argentière, Jean-Pierre Frijns, Griet Van Buggenhout, Annick Vogels, Koenraad Devriendt, Ann Swillen
Pages: 14 - 20 - Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood(2012)
Authors: Koenraad Devriendt, Jeroen Breckpot, Jean-Pierre Frijns, Hilde Peeters, Griet Van Buggenhout, Hilde Van Esch, Bea Maes, Ann Swillen
Pages: 135 - 148 - Genotype and Cardiovascular Phenotype Correlations with TBX1 in 1,022 Velo-Cardio-Facial/DiGeorge/22q11.2 Deletion Syndrome Patients(2011)
Authors: Koenraad Devriendt, Ann Swillen, Jeroen Breckpot
Pages: 1278 - 1289 - Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome(2011)
Authors: Koenraad Devriendt, Ann Swillen
Pages: 332 - 339