Ewout J. Groen
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 59 publications
The SMN locus in the T2T era: Structure, gene conversion, and clinical implications.
Journal: Trends in genetics : TIG
Published: January 30, 2026
Impaired renal function in patients with spinal muscular atrophy: A longitudinal cohort study.
Journal: Journal of neuromuscular diseases
Published: January 16, 2026
Safety through design: Expanding options for spinal muscular atrophy gene therapy.
Journal: Molecular therapy. Methods & clinical development
Published: September 02, 2025
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: August 15, 2025
Further Comments on Risdiplam for Prenatal Therapy of Spinal Muscular Atrophy.
Journal: The New England journal of medicine
Published: July 02, 2025
Dynamic modulation of the motor neuron translatome during developmental synapse elimination.
Journal: Science signaling
Published: April 15, 2025
A de novo deletion underlying spinal muscular atrophy: implications for carrier testing and genetic counseling.
Journal: Human molecular genetics
Published: January 30, 2025
Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophy.
Journal: Genome medicine
Published: September 18, 2024
Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoids.
Journal: Acta neuropathologica communications
Published: August 21, 2024
Patient-specific responses to SMN2 splice-modifying treatments in spinal muscular atrophy fibroblasts.
Journal: Molecular therapy. Methods & clinical development
Published: August 21, 2024
Last Updated: 09/26/2026