Dr David Harrison
Teams and roles for David Harrison
Research Associate
Neuroscience
Overview
My research interests span from the very early life environment to later life diseases, such as Parkinson's disease and Huntington's disease, and how these may be linked. Key words that pique my interest include: Neurodegeneration, neurodevelopment, placenta, epigenetics, prenatal adversity, microglia, preclinical behaviour and cognition.
I also have a keen interest in laboratory animal welfare and am committed to the NC3Rs.
Publication
2026
- Chibnall, A. et al. 2026. Sex-specific consequences of loss-of-imprinting of the maternally expressed gene Pleckstrin Homology-Like Domain Family A Member 2 (Phlda2) on placental development and fetal growth. Biology of Sex Differences (10.1186/s13293-026-00972-z)
2025
- Harrison, D. J. et al. 2025. Complex cognitive and motivational deficits precede motor dysfunction in the zQ175 (190 CAG repeat) Huntington's disease model.. Experimental Neurology 392 115350. (10.1016/j.expneurol.2025.115350)
- Paisey, S. J. et al. 2025. Imaging of human stem cell-derived dopamine grafts correlates with behavioural recovery and reveals microstructural brain changes. Neurobiology of Disease 209 106910. (10.1016/j.nbd.2025.106910)
2024
- Tyson, H. R. et al. 2024. Deficiency of the paternally-expressed imprinted Peg3 gene in mice has sexually dimorphic consequences for offspring communication and social behaviour. Frontiers in Neuroscience 18 1374781. (10.3389/fnins.2024.1374781)
2022
- Lane, E. L. et al. 2022. Spontaneous graft-induced dyskinesias are independent of 5-HT neurons and levodopa priming in a model of Parkinson's disease. Movement Disorders 37 (3), pp.613-619. (10.1002/mds.28856)
2021
- Harrison, D. J. et al. 2021. Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring. Human Molecular Genetics 30 (19), pp.1863-1880. ddab154. (10.1093/hmg/ddab154)
2020
- Harrison, D. J. et al. 2020. Unified behavioral scoring for preclinical models. Frontiers in Neuroscience 14 313. (10.3389/fnins.2020.00313)
2018
- Harrison, D. et al. 2018. The effect of tissue preparation and donor age on striatal graft morphology in the mouse. Cell Transplantation 27 (2), pp.230-244. (10.1177/0963689717744788)
- McNamara, G. I. et al. 2018. Loss of offspring Peg3 reduces neonatal ultrasonic vocalizations and increases maternal anxiety in wild-type mothers. Human Molecular Genetics 27 (3), pp.440-450. (10.1093/hmg/ddx412)
- Harrison, D. J. 2018. Optimisation of transplantation methodology in mouse models of Huntington’s Disease. PhD Thesis , Cardiff University.
2017
- Hensman Moss, D. J. et al., 2017. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Lancet Neurology 16 (9), pp.701-711. (10.1016/S1474-4422(17)30161-8)
- Trueman, R. C. et al., 2017. Systematic and detailed analysis of behavioural tests in the rat middle cerebral artery occlusion model of stroke: tests for long-term assessment. Journal of Cerebral Blood Flow and Metabolism 37 (4), pp.1349-1361. (10.1177/0271678X16654921)
- Ahmed, J. et al., 2017. Lickometry: a novel and sensitive method for assessing functional deficits in rats after stroke. Journal of Cerebral Blood Flow & Metabolism 37 (3), pp.755-761. (10.1177/0271678X16684141)
2016
- Bayram-Weston, Z. et al. 2016. Optimising Golgi-Cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington's disease. Journal of Neuroscience Methods 265 , pp.81-88. (10.1016/j.jneumeth.2015.09.033)
2015
- Steventon, J. et al. 2015. In Vivo MRI evidence that neuropathology is attenuated by cognitive enrichment in the Yac128 Huntington's Disease mouse model. Journal of Huntington's Disease 4 (2), pp.149-160. (10.3233/JHD-150147)
2013
- Roberton, V. H. et al. 2013. Is the adult mouse striatum a hostile host for neural transplant survival?. NeuroReport 24 (18), pp.1010-1015. (10.1097/WNR.0000000000000066)
- Harrison, D. J. et al. 2013. Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model. Experimental Neurology 248 , pp.457-469. (10.1016/j.expneurol.2013.07.014)
- Lelos, M. J. et al. 2013. The lateral neostriatum is necessary for compensatory ingestive behaviour after intravascular dehydration in female rats. Appetite 71 , pp.287-294. (10.1016/j.appet.2013.09.003)
2012
- Lelos, M. J. , Harrison, D. J. and Dunnett, S. B. 2012. Intrastriatal excitotoxic lesion or dopamine depletion of the neostriatum differentially impairs response execution in extrapersonal space. European Journal of Neuroscience 36 (10), pp.3420-3428. (10.1111/j.1460-9568.2012.08256.x)
2011
- Lelos, M. J. , Harrison, D. J. and Dunnett, S. B. 2011. Impaired sensitivity to Pavlovian stimulus-outcome learning after excitotoxic lesion of the ventrolateral neostriatum. Behavioural Brain Research 225 (2), pp.522-528. (10.1016/j.bbr.2011.08.017)
- Trueman, R. C. et al. 2011. A critical re-Examination of the intraluminal filament MCAO model: impact of External Carotid Artery transection. Translational Stroke Research 2 (4), pp.651-661. (10.1007/s12975-011-0102-4)
2002
- Armit, C. et al., 2002. Absence of p53 in Clara cells favours multinucleation and loss of cell cycle arrest. BMC Cell Biology 3 (27)(10.1186/1471-2121-3-27)
- Menke, A. et al., 2002. Genetic interactions between the Wilms’ Tumor 1 Gene and the p53 Gene. Cancer Research 62 (22), pp.6615-6620.
- Guo, J. et al., 2002. WT1 is a key regulator of podocyte function: Reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis. Human Molecular Genetics 11 (6), pp.651-659. (10.1093/hmg/11.6.651)
Articles
- Chibnall, A. et al. 2026. Sex-specific consequences of loss-of-imprinting of the maternally expressed gene Pleckstrin Homology-Like Domain Family A Member 2 (Phlda2) on placental development and fetal growth. Biology of Sex Differences (10.1186/s13293-026-00972-z)
- Harrison, D. J. et al. 2025. Complex cognitive and motivational deficits precede motor dysfunction in the zQ175 (190 CAG repeat) Huntington's disease model.. Experimental Neurology 392 115350. (10.1016/j.expneurol.2025.115350)
- Paisey, S. J. et al. 2025. Imaging of human stem cell-derived dopamine grafts correlates with behavioural recovery and reveals microstructural brain changes. Neurobiology of Disease 209 106910. (10.1016/j.nbd.2025.106910)
- Tyson, H. R. et al. 2024. Deficiency of the paternally-expressed imprinted Peg3 gene in mice has sexually dimorphic consequences for offspring communication and social behaviour. Frontiers in Neuroscience 18 1374781. (10.3389/fnins.2024.1374781)
- Lane, E. L. et al. 2022. Spontaneous graft-induced dyskinesias are independent of 5-HT neurons and levodopa priming in a model of Parkinson's disease. Movement Disorders 37 (3), pp.613-619. (10.1002/mds.28856)
- Harrison, D. J. et al. 2021. Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring. Human Molecular Genetics 30 (19), pp.1863-1880. ddab154. (10.1093/hmg/ddab154)
- Harrison, D. J. et al. 2020. Unified behavioral scoring for preclinical models. Frontiers in Neuroscience 14 313. (10.3389/fnins.2020.00313)
- Harrison, D. et al. 2018. The effect of tissue preparation and donor age on striatal graft morphology in the mouse. Cell Transplantation 27 (2), pp.230-244. (10.1177/0963689717744788)
- McNamara, G. I. et al. 2018. Loss of offspring Peg3 reduces neonatal ultrasonic vocalizations and increases maternal anxiety in wild-type mothers. Human Molecular Genetics 27 (3), pp.440-450. (10.1093/hmg/ddx412)
- Hensman Moss, D. J. et al., 2017. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Lancet Neurology 16 (9), pp.701-711. (10.1016/S1474-4422(17)30161-8)
- Trueman, R. C. et al., 2017. Systematic and detailed analysis of behavioural tests in the rat middle cerebral artery occlusion model of stroke: tests for long-term assessment. Journal of Cerebral Blood Flow and Metabolism 37 (4), pp.1349-1361. (10.1177/0271678X16654921)
- Ahmed, J. et al., 2017. Lickometry: a novel and sensitive method for assessing functional deficits in rats after stroke. Journal of Cerebral Blood Flow & Metabolism 37 (3), pp.755-761. (10.1177/0271678X16684141)
- Bayram-Weston, Z. et al. 2016. Optimising Golgi-Cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington's disease. Journal of Neuroscience Methods 265 , pp.81-88. (10.1016/j.jneumeth.2015.09.033)
- Steventon, J. et al. 2015. In Vivo MRI evidence that neuropathology is attenuated by cognitive enrichment in the Yac128 Huntington's Disease mouse model. Journal of Huntington's Disease 4 (2), pp.149-160. (10.3233/JHD-150147)
- Roberton, V. H. et al. 2013. Is the adult mouse striatum a hostile host for neural transplant survival?. NeuroReport 24 (18), pp.1010-1015. (10.1097/WNR.0000000000000066)
- Harrison, D. J. et al. 2013. Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model. Experimental Neurology 248 , pp.457-469. (10.1016/j.expneurol.2013.07.014)
- Lelos, M. J. et al. 2013. The lateral neostriatum is necessary for compensatory ingestive behaviour after intravascular dehydration in female rats. Appetite 71 , pp.287-294. (10.1016/j.appet.2013.09.003)
- Lelos, M. J. , Harrison, D. J. and Dunnett, S. B. 2012. Intrastriatal excitotoxic lesion or dopamine depletion of the neostriatum differentially impairs response execution in extrapersonal space. European Journal of Neuroscience 36 (10), pp.3420-3428. (10.1111/j.1460-9568.2012.08256.x)
- Lelos, M. J. , Harrison, D. J. and Dunnett, S. B. 2011. Impaired sensitivity to Pavlovian stimulus-outcome learning after excitotoxic lesion of the ventrolateral neostriatum. Behavioural Brain Research 225 (2), pp.522-528. (10.1016/j.bbr.2011.08.017)
- Trueman, R. C. et al. 2011. A critical re-Examination of the intraluminal filament MCAO model: impact of External Carotid Artery transection. Translational Stroke Research 2 (4), pp.651-661. (10.1007/s12975-011-0102-4)
- Armit, C. et al., 2002. Absence of p53 in Clara cells favours multinucleation and loss of cell cycle arrest. BMC Cell Biology 3 (27)(10.1186/1471-2121-3-27)
- Menke, A. et al., 2002. Genetic interactions between the Wilms’ Tumor 1 Gene and the p53 Gene. Cancer Research 62 (22), pp.6615-6620.
- Guo, J. et al., 2002. WT1 is a key regulator of podocyte function: Reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis. Human Molecular Genetics 11 (6), pp.651-659. (10.1093/hmg/11.6.651)
Thesis
- Harrison, D. J. 2018. Optimisation of transplantation methodology in mouse models of Huntington’s Disease. PhD Thesis , Cardiff University.
Contact Details
[email protected]
Sir Martin Evans Building, Room 4.01, Museum Avenue, Cardiff, CF10 3AX
Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ
Sir Martin Evans Building, Room 4.01, Museum Avenue, Cardiff, CF10 3AX
Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ