Lies Vantomme

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 14 publications

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

Journal: Nature communications

Published: March 25, 2025

De Novo CUL3 Variant in a Child Presenting With Hypertension and Kidney Failure.

De Novo CUL3 Variant in a Child Presenting With Hypertension and Kidney Failure.

Journal: Kidney international reports

Published: December 02, 2024

Cracking rare disorders: a new minimally invasive RNA-seq protocol.

Cracking rare disorders: a new minimally invasive RNA-seq protocol.

Journal: NPJ genomic medicine

Published: November 18, 2024

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: August 16, 2024

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.

Journal: American journal of human genetics

Published: August 09, 2024

Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping.

Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping.

Journal: Scientific reports

Published: July 20, 2024

Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum.

Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum.

Journal: Cell reports. Medicine

Published: September 19, 2023

Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci.

Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci.

Journal: Genome biology

Published: June 30, 2023

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene.

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene.

Journal: medRxiv : the preprint server for health sciences

Published: June 09, 2023

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.

Journal: American journal of human genetics

Published: June 07, 2023

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics.

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics.

Journal: Human molecular genetics

Published: September 07, 2018

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristics.

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristics.

Journal: Human molecular genetics

Published: September 07, 2018

Showing 1-12 of 14

Last Updated: 09/26/2026