Eva D'haene

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 15 publications

Retina-specific long non-coding RNAs associated with inherited retinal disease genes.

Retina-specific long non-coding RNAs associated with inherited retinal disease genes.

Journal: Cellular and molecular life sciences : CMLS

Published: February 13, 2026

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

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

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

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy.

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy.

Journal: American journal of human genetics

Published: May 26, 2022

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development.

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development.

Journal: Nature communications

Published: March 24, 2022

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models.

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models.

Journal: American journal of human genetics

Published: February 15, 2022

HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations.

HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations.

Journal: Genome research

Published: September 12, 2021

SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitry.

SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitry.

Journal: Nature communications

Published: August 14, 2020

Interpreting the impact of noncoding structural variation in neurodevelopmental disorders.

Interpreting the impact of noncoding structural variation in neurodevelopmental disorders.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 09, 2020

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 15

Last Updated: 09/26/2026