Wouter De Coster

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 33 publications

A comprehensive assessment of tandem repeat genotyping methods for Nanopore long-read genomes.

A comprehensive assessment of tandem repeat genotyping methods for Nanopore long-read genomes.

Journal: bioRxiv : the preprint server for biology
Published: March 23, 2026

Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15.

Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15.

Journal: bioRxiv : the preprint server for biology
Published: February 06, 2026

Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U.

Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U.

Journal: Acta neuropathologica
Published: July 02, 2025

Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron disease.

Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron disease.

Journal: Acta neuropathologica
Published: June 26, 2025

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions.

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions.

Journal: Nature genetics
Published: February 21, 2025

Methylmap: visualization of modified nucleotides for large cohort sizes.

Methylmap: visualization of modified nucleotides for large cohort sizes.

Journal: BMC bioinformatics
Published: January 08, 2025

Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.

Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.

Journal: Molecular neurodegeneration
Published: December 10, 2024

Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health.

Increased TMEM106B levels lead to lysosomal dysfunction which affects synaptic signaling and neuronal health.

Journal: Molecular neurodegeneration
Published: August 28, 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

Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.

Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.

Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2024

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.

Journal: Nature communications
Published: June 05, 2024

Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing.

Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing.

Journal: Bioinformatics (Oxford, England)
Published: April 23, 2024
Showing 1-12 of 33

Last Updated: 09/26/2026