Wouter Van Rheenen
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 87 publications
Lessons from a systematic review of family-based studies in ALS.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 12, 2026
Tofersen treatment in respiratory onset amyotrophic lateral sclerosis and a variant of uncertain significance in SOD1; a case report.
Journal: European journal of human genetics : EJHG
Published: April 28, 2026
Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALS.
Journal: BMJ neurology open
Published: November 11, 2025
Reader Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype.
Journal: Neurology
Published: October 03, 2025
Dissecting epigenetic age acceleration in amyotrophic lateral sclerosis.
Journal: Epigenomics
Published: September 30, 2025
A VAPB (P56S) mutation in a Dutch patient with familial motor neuron disease: a case report.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: September 04, 2025
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: August 15, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosis.
Journal: Brain communications
Published: May 01, 2025
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.
Journal: bioRxiv : the preprint server for biology
Published: December 09, 2024
An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2.
Journal: European journal of human genetics : EJHG
Published: November 08, 2024
Last Updated: 09/26/2026