Researcher
Hilde Peeters
- Disciplines:Genetic predisposition, Clinical genetics and molecular diagnostics, Genetics
Affiliations
- Laboratory for Genetic Epidemiology (Division)
Responsible
From1 Jan 2013 → Today - Laboratory for Genetics of Human Development (Division)
Member
From1 Apr 2009 → 30 Sep 2010 - Department of Human Genetics (Department)
Member
From1 Oct 2000 → Today
Projects
1 - 10 of 17
- Age and sex-appropriate 3D shape analysis and geometric deep learning for children undergoing craniofacial diagnostics and surgeryFrom1 Jan 2023 → TodayFunding: FWO research project (including WEAVE projects)
- Assessment of the contribution of developmental enhancers in craniofacial disordersFrom1 Jul 2022 → TodayFunding: FWO fellowships
- 3D craniofacial phenotypes in genetic diagnosticsFrom1 Jan 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Data-driven search for 3D facial traits determined by major gene effects in health and diseaseFrom1 Oct 2020 → TodayFunding: BOF - projects
- Ethical challenges of precision medicineFrom1 Feb 2020 → 3 May 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- MOLECULAR DIAGNOSTICS IN AUTISM SPECTRUM DISORDER: NEXT GENERATION SEQUENCING AND FACIAL PHENOTYPING IN MEDICAL GENETICSFrom1 Oct 2018 → 24 Oct 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- Part-Based Syndrome Classification and Metric Spaces: Linear 3D Facial Analysis vs Geometric Deep LearningFrom1 Sep 2018 → 27 Oct 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- Implementation of an expanded carrier screening offer for couplesFrom1 Jan 2018 → 31 Dec 2021Funding: FWO research project (including WEAVE projects)
- Risk assessment of autism spectrum disorder in infantsFrom1 Oct 2017 → 30 Sep 2021Funding: FWO Strategic Basic Research (SBO)
- The genetic architecture of normal facial variation in relation to orofacial cleftingFrom24 Oct 2016 → 19 Nov 2020Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
101 - 110 of 127
- Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example(2013)
Authors: Veerle De Wolf, Nathalie Brison, Koenraad Devriendt, Hilde Peeters
Pages: 2846 - 54 - Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiency(2013)
Authors: Magdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, Hilde Peeters, Marleen Renard, Eline Beert, Hilde Brems, Tina Giner, Imke Bieber, Henning Hamm, et al.
Pages: 656 - 664 - Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiency(2013)
Authors: Magdalena Chmara, Bartosz Wasag, Hilde Peeters, Eline Beert, Hilde Brems, Raf Sciot, Eric Legius
Pages: 656 - 664 - Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders(2013)
Authors: Hilde Peeters
Pages: 1960 - 1970 - The East Flanders Prospective Twin Survey (EFPTS): An Actual Perception(2013)
Authors: Cathérine Derom, Hilde Peeters, Robert Vlietinck, Jean-Pierre Frijns
Pages: 58 - 63 - Genetische counseling(2013)
Authors: Hilde Peeters, Koenraad Devriendt
Pages: 195 - 206 - Congenital High Airway Obstruction Syndrome (CHAOS) as part of Fraser syndrome: ultrasound and autopsy findings(2013)
Authors: Ingrid Witters, Hilde Peeters, Jean-Pierre Frijns
Pages: 367 - 71 - NRAS Mutations in Noonan Syndrome(2012)
Authors: Ellen Denayer, Hilde Peeters, Jean-Pierre Frijns, Eric Legius
Pages: 34 - 38 - 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 - Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms(2012)
Authors: Mala Isrie, Hilde Peeters, Joris Vermeesch, Hilde Van Esch
Pages: 131 - 133