Ligia M. Mateiu
Antwerpen, VLG, Belgium
Last Updated: 09/26/2026
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Found 35 publications
Correction: A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.
Journal: European journal of human genetics : EJHG
Published: March 31, 2026
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.
Journal: Annals of neurology
Published: August 25, 2025
The ADNP-Mediated Transcriptome Response to Ketamine Impairs the Cytoskeletal Protein Axis.
Journal: Journal of molecular neuroscience : MN
Published: August 20, 2025
An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice.
Journal: EBioMedicine
Published: July 15, 2025
Time-Series Transcriptome Analysis of the Older Adult Mouse Cochlea After Noise-Induced Hearing Loss Reveals an Acute Immune Response and Recovery-Associated Pathways.
Journal: Molecular neurobiology
Published: June 17, 2025
Gradual DNA methylation changes reveal transcription factors implicated in metabolic dysfunction-associated steatotic liver disease progression and epigenetic age acceleration.
Journal: Clinical epigenetics
Published: May 08, 2025
A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study.
Journal: Clinical epigenetics
Published: April 11, 2025
Comparison of current methods for genome-wide DNA methylation profiling.
Journal: Epigenetics & chromatin
Published: March 13, 2025
A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.
Journal: European journal of human genetics : EJHG
Published: February 11, 2025
A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.
Journal: European journal of human genetics : EJHG
Published: February 11, 2025
RNA sequencing offers new diagnostic opportunities in neurodevelopmental disorders: A systematic review.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 28, 2024
Correction to: ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van Der Aa syndrome autopsy case.
Journal: Acta neuropathologica communications
Published: October 25, 2024
Last Updated: 09/26/2026