Rodrigo M. Young
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 19 publications
frizzled 5 mutant zebrafish are genetically sensitised to developing microphthalmia and coloboma.
Journal: Disease models & mechanisms
Published: January 06, 2025
Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: November 28, 2024
Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome.
Journal: Research square
Published: November 28, 2024
Variants in NR6A1 cause a novel oculo vertebral renal syndrome.
Journal: Nature communications
Published: November 09, 2024
Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brain.
Journal: Science (New York, N.Y.)
Published: May 02, 2024
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina.
Journal: The Journal of pathology
Published: July 29, 2022
Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 17, 2021
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility Study.
Journal: JMIR formative research
Published: June 11, 2020
Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variants.
Journal: Clinical genetics
Published: April 29, 2020
Tissue-Specific Requirement for the GINS Complex During Zebrafish Development.
Journal: Frontiers in cell and developmental biology
Published: February 21, 2020
Last Updated: 09/26/2026