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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
31 - 40 of 127
- Insights into the genetic architecture of the human face(2021)
Authors: Karlijne Indencleef, Hanne Hoskens, Jiarui Li, Hilde Peeters, Greet Hens, Peter Claes
- Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders(2020)
Authors: Hilde Peeters
Pages: 3 - 4 - The genetic architecture of normal facial variation in relation to orofacial clefting(2020)
Authors: Karlijne Indencleef, Peter Claes, Hilde Peeters, Greet Hens
- NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism(2020)
Authors: Hilde Peeters
Pages: 963 - 976 - A de-novo 15q24.2 deletion involving SIN3A is associated with emotional, behavioural, motor problems and hypersensitivity in a girl with above average intelligence and typical facial features.(2020)
Authors: Yoeri Sleyp, Ann Swillen, Kris Van Den Bogaert, Hilde Peeters
Pages: 210 - 213 - Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders(2020)
Authors: Yoeri Sleyp, Hilde Peeters
- Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder(2020)
Authors: Hilde Peeters
Pages: 2437 - 2453 - Frequency and Management of Craniofacial Syndromes(2020)
Authors: Carine Carels, Hilde Peeters, Constantinus Politis
Pages: 1091 - 1097 - The clinical relevance of intragenic NRXN1 deletions(2020)
Authors: Nele Cosemans, Annick Vogels, Koenraad Devriendt, Hilde Van Esch, Griet Van Buggenhout, Thomy de Ravel de l'Argentière, Els Ortibus, Eric Legius, Jeroen Breckpot, Joris Vermeesch, et al.
Pages: 347 - 355 - Interest in expanded carrier screening among individuals and couples in the general population : systematic review of the literature(2020)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
Pages: 335 - 355