Last Updated: 09/26/2026
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Found 32 publications
RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs).
Journal: bioRxiv : the preprint server for biology
Published: July 15, 2025
RetiGene, a comprehensive gene atlas for inherited retinal diseases.
Journal: American journal of human genetics
Published: June 10, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 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
Neutralization and Anti-S Antibody Titers in SARS-CoV-2 Boosted Adults in Mexico: A Comparison Across Five Vaccine Types.
Journal: International journal of microbiology
Published: September 29, 2024
Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases.
Journal: Human molecular genetics
Published: January 08, 2024
Systematic assessment of the contribution of structural variants to inherited retinal diseases.
Journal: bioRxiv : the preprint server for biology
Published: February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseases.
Journal: Human molecular genetics
Published: October 24, 2022
PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy.
Journal: European journal of medical genetics
Published: May 25, 2021
Last Updated: 09/26/2026