Marc Folcher
Basel, BS, Switzerland
Last Updated: 09/26/2026
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Found 27 publications
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvement.
Journal: American journal of human genetics
Published: August 13, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
Encapsulated cells as an enzyme replacement therapy for metachromatic leukodystrophy.
Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: April 14, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.
Journal: medRxiv : the preprint server for health sciences
Published: January 20, 2025
Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa.
Journal: American journal of human genetics
Published: May 01, 2024
Bioelectronic cell-based device provides a strategy for the treatment of the experimental model of multiple sclerosis.
Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: August 12, 2022
The Potential Cost-Effectiveness of a Cell-Based Bioelectronic Implantable Device Delivering Interferon-β1a Therapy Versus Injectable Interferon-β1a Treatment in Relapsing-Remitting Multiple Sclerosis.
Journal: PharmacoEconomics
Published: August 10, 2021
Optimized Protocol for Subcutaneous Implantation of Encapsulated Cells Device and Evaluation of Biocompatibility.
Journal: Frontiers in bioengineering and biotechnology
Published: January 07, 2021
Genomic and transcriptomic landscape of conjunctival melanoma.
Journal: PLoS genetics
Published: February 21, 2020
Last Updated: 09/26/2026