A multi-omics approach to address the role of ZFHX3 in neuronal development

IMAGIBRAINDD: IMAGIng-assisted human BRAIn organoid engineering for studying and treating NeuroDevelopmental Disorders

Regulatory landscaping: Towards improved genetic diagnosis and therapy for SATB2-associated syndrome

Addressing the missing heritability in rare disorders

A multi-omics approach to address neuronal development upon ZFHX3 deficiency

Delineating the regulatory landscape of SATB2

Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndrome

Steunfonds Marguerite-Marie Delacroix: A multi-omics approach to address neuronal development upon ZFHX4 deficiency

Steunfonds Marguerite-Marie Delacroix: Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndrome (Lisa Hamerlinck)

Unveiling the role of FOXG1 in neurodevelopment and disease: a comprehensive analysis using neural organoids, imaging and Single Cell Sequencing

3D-RET: unlocking 3D genome architecture in human retina using C-technologies

Incucyte S3: Comprehensive cellular phenotyping using high-throughput live cell imaging

Lab equipment necessary for the generation, manipulation and genome editing of pluripotent stem cells

Research equipment for behavior analysis in zebrafish disease models.

The role of long noncoding RNAs in human cognition

Functional validation of cis-regulatory elements of respectively MEF2C and FOXG1

Identification of causal mutations in patients with unexplained mental retardation and congenital abnormalities by high throughput sequencing of selected candidate genes

The role of lncRNAs in human cognition

The role of long noncoding RNAs in human cognition

Precision medicine in inherited blindness using integrated omics in human and animal models