Alfredo Rey-Duenas

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 11 publications

Retina-specific long non-coding RNAs associated with inherited retinal disease genes.

Retina-specific long non-coding RNAs associated with inherited retinal disease genes.

Journal: Cellular and molecular life sciences : CMLS

Published: February 13, 2026

DA.Vra1-congenic rats display increased gene expression and Schwann cell apoptosis but unaffected nerve regeneration compared to parental DA rats after sciatic nerve injury and repair.

DA.Vra1-congenic rats display increased gene expression and Schwann cell apoptosis but unaffected nerve regeneration compared to parental DA rats after sciatic nerve injury and repair.

Journal: Frontiers in cell and developmental biology

Published: November 28, 2024

Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches.

Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches.

Journal: Genome research

Published: September 24, 2024

Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci.

Author Correction: Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci.

Journal: Nature communications

Published: May 10, 2024

Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform.

Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform.

Journal: Clinical genetics

Published: December 20, 2023

Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson's disease reveal upregulation of oxidative phosphorylation-related genes associated with delayed dopaminergic neurodegeneration.

Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson's disease reveal upregulation of oxidative phosphorylation-related genes associated with delayed dopaminergic neurodegeneration.

Journal: Frontiers in aging neuroscience

Published: November 12, 2023

Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci.

Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci.

Journal: Nature communications

Published: October 01, 2023

Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease.

Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease.

Journal: Genome medicine

Published: June 16, 2023

Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish.

Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish.

Journal: Frontiers in neuroscience

Published: April 17, 2023

The MHC class II transactivator modulates seeded alpha-synuclein pathology and dopaminergic neurodegeneration in an in vivo rat model of Parkinson's disease.

The MHC class II transactivator modulates seeded alpha-synuclein pathology and dopaminergic neurodegeneration in an in vivo rat model of Parkinson's disease.

Journal: Brain, behavior, and immunity

Published: June 12, 2020

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.

Journal: American journal of human genetics

Published: March 06, 2020

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Last Updated: 09/26/2026