Wim Robberecht
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 105 publications
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.
Journal: Neurobiology of disease
Published: October 15, 2022
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.
Journal: Frontiers in cellular neuroscience
Published: September 21, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.
Journal: Nature communications
Published: February 01, 2022
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Journal: JAMA neurology
Published: August 30, 2021
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed.
Journal: Brain communications
Published: February 27, 2021
STING-Induced Inflammation - A Novel Therapeutic Target in ALS?
Journal: The New England journal of medicine
Published: February 24, 2021
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.
Journal: NPJ genomic medicine
Published: December 15, 2020
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.
Journal: Annals of neurology
Published: September 11, 2020
AAV9-mediated gene delivery of MCT1 to oligodendrocytes does not provide a therapeutic benefit in a mouse model of ALS.
Journal: Molecular therapy. Methods & clinical development
Published: August 18, 2020
Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4V.
Journal: Protein engineering, design & selection : PEDS
Published: March 26, 2020
Last Updated: 09/26/2026