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Researcher
Yoeri Sleyp
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Department of Human Genetics (Department)
Member
From1 Oct 2021 → Today - Laboratory for Genetic Epidemiology (Division)
Member
From1 Oct 2018 → Today
Projects
1 - 1 of 1
- 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
Publications
1 - 5 of 5
- De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder(2022)
Authors: Yoeri Sleyp, Patrick Callaerts, Jarymke Maljaars, Frederic Rousseau, Joost Schymkowitz, Erika Souche, Jean Steyaert, Hilde Peeters
Pages: 2464 - 2474 - MOLECULAR DIAGNOSTICS IN AUTISM SPECTRUM DISORDER: NEXT GENERATION SEQUENCING AND FACIAL PHENOTYPING IN MEDICAL GENETICS(2022)
Authors: Yoeri Sleyp, Hilde Peeters, Peter Claes
- Shared heritability of human face and brain shape(2021)
Authors: Yoeri Sleyp, Hanne Hoskens, Rose Bruffaerts, Ahmed Radwan, Stefan Sunaert, Hilde Peeters, Peter Claes
Pages: 830 - + - 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