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
91 - 100 of 127
- Review: Facial endophenotypes in non-syndromic orofacial clefting(2015)
Authors: Jasmien Roosenboom, Peter Claes, Koenraad Devriendt, T Dormaar, Hilde Peeters, Ine Saey, Joseph Schoenaers, Vincent Vander Poorten, Anna Verdonck, Greet Hens
Pages: 173 - 182 - A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism(2014)
Authors: Veerle De Wolf, An Crepel, Frans Schuit, Leentje van Lommel, Berten Ceulemans, Jean Steyaert, Eve Seuntjens, Hilde Peeters, Koenraad Devriendt
Pages: 3035 - 41 - A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism(2014)
Authors: Veerle De Wolf, Frans Schuit, Jean Steyaert, Eve Seuntjens, Hilde Peeters, Koenraad Devriendt
Pages: 3035 - 41 - Refining analyses of copy number variation identifies specific genes associated with developmental delay(2014)
Authors: Hilde Peeters
Pages: 1063 - 71 - The Communication of Secondary Variants: Interviews with Parents whose Children have Undergone Array-CGH Testing(2014)
Authors: Koenraad Devriendt, Hilde Peeters, Hilde Van Esch, Kris Dierickx
Pages: 207 - 16 - Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings(2014)
Authors: Jacoba Louw, Yaojuan Jia, Marc Gewillig, Hilde Peeters, Philippe Moerman, Koenraad Devriendt
Pages: 532 - 5 - Association of CDH11 with non-syndromic ASD(2014)
Authors: Veerle De Wolf, Nathalie Brison, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koenraad Devriendt, Hilde Peeters
Pages: 391 - 8 - Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development(2014)
Authors: Hilde Peeters, Jean Steyaert
Pages: 263 - 76 - Association of CDH11 with non-syndromic ASD(2014)
Authors: An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koenraad Devriendt, et al.
Pages: 391 - 8 - 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