Robert I. Richards
Adelaide, SA, Australia
Last Updated: 09/26/2026
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Found 20 publications
Single-cell sequencing shows mosaic aneuploidy in most human embryos.
Journal: The Journal of clinical investigation
Published: March 15, 2024
Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D.
Journal: Cells
Published: April 09, 2021
Zebrafish Chromosome 14 Gene Differential Expression in the fmr1 h u2787 Model of Fragile X Syndrome.
Journal: Frontiers in genetics
Published: November 03, 2020
Non-self mutation: double-stranded RNA elicits antiviral pathogenic response in a Drosophila model of expanded CAG repeat neurodegenerative diseases.
Journal: Human molecular genetics
Published: February 22, 2019
Neurodegenerative diseases have genetic hallmarks of autoinflammatory disease.
Journal: Human molecular genetics
Published: March 12, 2018
Neuronal-specific impairment of heparan sulfate degradation in Drosophila reveals pathogenic mechanisms for Mucopolysaccharidosis type IIIA.
Journal: Experimental neurology
Published: October 12, 2016
The Enemy within: Innate Surveillance-Mediated Cell Death, the Common Mechanism of Neurodegenerative Disease.
Journal: Frontiers in neuroscience
Published: March 16, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Journal: Autophagy
Published: January 23, 2016
Tumor suppressor WWOX moderates the mitochondrial respiratory complex.
Journal: Genes, chromosomes & cancer
Published: April 29, 2015
WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancer.
Journal: Experimental biology and medicine (Maywood, N.J.)
Published: January 18, 2015
RNA pathogenesis via Toll-like receptor-activated inflammation in expanded repeat neurodegenerative diseases.
Journal: Frontiers in molecular neuroscience
Published: July 22, 2013
Last Updated: 09/26/2026