Yoeri Sleyp
Leuven, VLG, Belgium
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: June 10, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome.
Journal: Journal of medical genetics
Published: May 20, 2025
Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder.
Journal: Clinical genetics
Published: April 28, 2024
De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 07, 2022
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Journal: Nature communications
Published: October 22, 2020
Shared heritability of human face and brain shape.
Journal: Nature genetics
Published: August 29, 2020
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.
Journal: Clinical dysmorphology
Published: July 09, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Journal: Nature communications
Published: April 09, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026