Rose Richardson

University of Manchester — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

13h-index770citations30works2.02yr avg
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Research Topics

Retinal Development and Disorders(9), Prion Diseases and Protein Misfolding(5), Parkinson's Disease Mechanisms and Treatments(4), Alzheimer's disease research and treatments(4), Circadian rhythm and melatonin(4)

Publications30 total

A cellular basis for the mammalian nocturnal-diurnal switch
Science·2026Open Access
Altered proportions of retinal cell types and distinct visual codes in rodents occupying divergent ecological niches
Current Biology·2025· 6 citedOpen Access
Reconfiguration of the visual code and retinal cell type complement in closely related diurnal and nocturnal mice
2024Open Access
Evolution of neuronal cell classes and types in the vertebrate retina
Nature·2023· 170 citedOpen Access
The genomic basis of temporal niche evolution in a diurnal rodent
Current Biology·2023· 13 citedOpen Access
Thermosensitivity of translation underlies the mammalian nocturnal-diurnal switch
2023· 9 citedOpen Access
Evolution of neuronal cell classes and types in the vertebrate retina
2023· 33 citedOpen Access
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina
The Journal of Pathology·2023· 11 citedOpen Access
Distinguishing post‐translational modifications in dominantly inherited frontotemporal dementias: FTLD‐TDP Type A ( <i>GRN</i> ) vs Type B ( <i>C9orf72</i> )
Neuropathology and Applied Neurobiology·2022· 11 citedOpen Access
REP1 deficiency causes systemic dysfunction of lipid metabolism and oxidative stress in choroideremia
JCI Insight·2021· 18 citedOpen Access
Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T Mutation
Journal of Neuropathology & Experimental Neurology·2019· 9 citedOpen Access
Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T Mutation
PMC·2019
Phagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathy
Scientific Reports·2019· 28 citedOpen Access
Transcriptome profiling of zebrafish optic fissure fusion
Scientific Reports·2019· 26 citedOpen Access
Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [18F]Flortaucipir PET
Acta Neuropathologica Communications·2018· 16 citedOpen Access
Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [18F]Flortaucipir PET
PMC·2018· 1 citedOpen Access
p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palate
PLoS Genetics·2017· 51 citedOpen Access
Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches
European Journal of Human Genetics·2017· 17 citedOpen Access
Mechanism and evidence of nonsense suppression therapy for genetic eye disorders
Experimental Eye Research·2017· 43 cited
Longitudinal phenotypic analysis of the early onset retinal degeneration in the homozygous kcnj13-/- zebrafish model
UCL Discovery (University College London)·2016
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Frequent Co-authors

Bernardino Ghetti(12), Jill R. Murrell(10), Mariya Moosajee(9), Francine Epperson(9), Adrian L. Oblak(8), Dhani Tracey‐White(7), Robert J. Lucas(5), Martin R. Farlow(5), Frederick W. Unverzagt(5), Andrew R. Webster(4), Joshua Hahn(4), Aboozar Monavarfeshani(4), Joshua R. Sanes(4), Karthik Shekhar(4), Maria Toms(4), Shannon L. Risacher(4), Andrew J. Saykin(4), Wenjun Yan(3), Nicholas Owen(3), Beatriz Baño‐Otálora(3)