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
41 - 50 of 127
- Increased Ca2+ signaling in NRXN1a(+/-) neurons derived from ASD induced pluripotent stem cells(2019)
Authors: Nele Cosemans, Hilde Peeters
- Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening(2019)
Authors: Nathalie Brison, Kristl Claeys, Thomy de Ravel de l'Argentière, Liesbeth De Waele, Nathalie Goemans, Eric Legius, Hilde Peeters, Hilde Van Esch, Joris Vermeesch, Koenraad Devriendt, et al.
Pages: 2774 - 2780 - The East Flanders Prospective Twin Survey (EFPTS): 55 Years Later(2019)
Authors: Hilde Peeters
Pages: 454 - 459 - Monoclonal gammopathy of renal significance (MGRS): histopathologic classification, diagnostic workup, and therapeutic options(2019)
Authors: Hilde Peeters, Ben Sprangers
Pages: 243 - 254 - Adolescent met schizofreniformestoornis en terugkerende 16p11.2-duplicatie [Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication](2019)
Authors: Jean Steyaert, Hilde Peeters, Griet Van Buggenhout
Pages: 421 - 425 - Het gezicht tussen beeld en werkelijkheid: Maatschappelijke verwachtingen.(2019)
Authors: Constantinus Politis, Hilde Peeters, Bart Pattyn, Pieter d'Hoine
Pages: 215 - 241Number of pages: 26 - Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo(2019)
Authors: Hilde Peeters, Koenraad Devriendt
Pages: 153 - 159 - Spatially-Dense 3D Facial Heritability and Modules of Co-Heritability in a Father-Offspring Design(2018)
Authors: Hanne Hoskens, Jiarui Li, Karlijne Indencleef, Dorothy Gors, Maarten Larmuseau, Greet Hens, Hilde Peeters, Peter Claes
- NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly(2018)
Authors: Vincent Gatinois, Hilde Peeters
Pages: 752 - 768 - Six NSCL/P loci show associations with normal-range craniofacial variation(2018)
Authors: Karlijne Indencleef, Hanne Hoskens, Hilde Peeters, Greet Hens, Peter Claes