Dr Cynthia Sandor
Sêr Cymru Fellow, Dementia Research Institute
- SandorC@cardiff.ac.uk
- Hadyn Ellis Building, Room 1.03 - Desk 30, Maindy Road, Cardiff, CF24 4HQ
Publication
2023
- MacIver, C. et al. 2023. Macro- and micro-structural Insights into primary dystonia A UK Biobank study. Journal of Neurology (10.1007/s00415-023-12086-2)
- Schalkamp, A., Peall, K. J., Harrison, N. A. and Sandor, C. 2023. Wearable movement-tracking data identify Parkinson's disease years before clinical diagnosis. Nature Medicine 29, pp. 2048-2056. (10.1038/s41591-023-02440-2)
- Bettencourt, C. et al. 2023. Artificial intelligence for dementia genetics and omics. Alzheimer's & Dementia: The Journal of the Alzheimer's Association (10.1002/alz.13427)
- Stevenson-Hoare, J., Schalkamp, A., Sandor, C., Hardy, J. and Escott-Price, V. 2023. New cases of dementia are rising in elderly populations in Wales, UK. Journal of the Neurological Sciences 451, article number: 120715. (10.1016/j.jns.2023.120715)
2022
- Wadon, M., Fenner, E., Kendall, K., Bailey, G., Sandor, C., Rees, E. and Peall, K. J. 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269, pp. 6436-6451. (10.1007/s00415-022-11307-4)
- Sandor, C. et al. 2022. Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine 14, article number: 129. (10.1186/s13073-022-01132-9)
- Schalkamp, A., Rahman, N., Monzón-Sandoval, J. and Sandor, C. 2022. Deep phenotyping for precision medicine in Parkinson's disease. Disease Models and Mechanisms 15(6), article number: dmm049376. (10.1242/dmm.049376)
2021
- Wadon, M. E. et al. 2021. Non-motor phenotypic subgroups in adult-onset idiopathic, isolated, focal cervical dystonia. Brain and Behavior 11(8), article number: e2292. (10.1002/brb3.2292)
2020
- Ward, J. et al. 2020. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Molecular Psychiatry 25, pp. 3091-3099. (10.1038/s41380-019-0439-8)
- Agarwal, D. et al. 2020. A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders. Nature Communications 11(1), article number: 4183. (10.1038/s41467-020-17876-0)
- Carling, P. J. et al. 2020. Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease. Progress in Neurobiology 187, article number: 101772. (10.1016/j.pneurobio.2020.101772)
- Williams, N. M. et al. 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35(4), pp. 705-707. (10.1002/mds.28001)
2018
- Eddowes, L. A. et al. 2018. Antiviral activity of bone morphogenetic proteins and activins. Nature Microbiology 4, pp. 339-351. (10.1038/s41564-018-0301-9)
- Volpato, V. et al. 2018. Reproducibility of molecular phenotypes after long-term differentiation to uuman iPSC-derived neurons: a multi-site omics study. Stem Cell Reports 11(4), pp. 897-911. (10.1016/j.stemcr.2018.08.013)
- Yang, Y. et al. 2018. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics 26(8), pp. 1202-1216. (10.1038/s41431-018-0150-2)
- Anttila, V. et al. 2018. Analysis of shared heritability in common disorders of the brain. Science 360(6395), article number: eaap8757. (10.1126/science.aap8757)
2017
- Sandor, C., Beer, N. L. and Webber, C. 2017. Diverse type 2 diabetes genetic risk factors functionally converge in a phenotype-focused gene network. PLoS Computational Biology 13(10), article number: e1005816. (10.1371/journal.pcbi.1005816)
- Sandor, C. et al. 2017. Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease. Human Molecular Genetics 26(3), pp. 552-566. (10.1093/hmg/ddw412)
- Sandor, C. et al. 2017. Whole-exome sequencing of 228 patients with sporadic Parkinson's disease. Scientific Reports 7, article number: 41188. (10.1038/srep41188)
2016
- Gormley, P. et al. 2016. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48(10), pp. 1296. (10.1038/ng1016-1296c)
- Gormley, P. et al. 2016. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48(8), pp. 856-866. (10.1038/ng.3598)
2012
- Eyre, S. et al. 2012. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics 44(12), pp. 1336-1340. (10.1038/ng.2462)
Articles
- MacIver, C. et al. 2023. Macro- and micro-structural Insights into primary dystonia A UK Biobank study. Journal of Neurology (10.1007/s00415-023-12086-2)
- Schalkamp, A., Peall, K. J., Harrison, N. A. and Sandor, C. 2023. Wearable movement-tracking data identify Parkinson's disease years before clinical diagnosis. Nature Medicine 29, pp. 2048-2056. (10.1038/s41591-023-02440-2)
- Bettencourt, C. et al. 2023. Artificial intelligence for dementia genetics and omics. Alzheimer's & Dementia: The Journal of the Alzheimer's Association (10.1002/alz.13427)
- Stevenson-Hoare, J., Schalkamp, A., Sandor, C., Hardy, J. and Escott-Price, V. 2023. New cases of dementia are rising in elderly populations in Wales, UK. Journal of the Neurological Sciences 451, article number: 120715. (10.1016/j.jns.2023.120715)
- Wadon, M., Fenner, E., Kendall, K., Bailey, G., Sandor, C., Rees, E. and Peall, K. J. 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269, pp. 6436-6451. (10.1007/s00415-022-11307-4)
- Sandor, C. et al. 2022. Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine 14, article number: 129. (10.1186/s13073-022-01132-9)
- Schalkamp, A., Rahman, N., Monzón-Sandoval, J. and Sandor, C. 2022. Deep phenotyping for precision medicine in Parkinson's disease. Disease Models and Mechanisms 15(6), article number: dmm049376. (10.1242/dmm.049376)
- Wadon, M. E. et al. 2021. Non-motor phenotypic subgroups in adult-onset idiopathic, isolated, focal cervical dystonia. Brain and Behavior 11(8), article number: e2292. (10.1002/brb3.2292)
- Ward, J. et al. 2020. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Molecular Psychiatry 25, pp. 3091-3099. (10.1038/s41380-019-0439-8)
- Agarwal, D. et al. 2020. A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders. Nature Communications 11(1), article number: 4183. (10.1038/s41467-020-17876-0)
- Carling, P. J. et al. 2020. Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease. Progress in Neurobiology 187, article number: 101772. (10.1016/j.pneurobio.2020.101772)
- Williams, N. M. et al. 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35(4), pp. 705-707. (10.1002/mds.28001)
- Eddowes, L. A. et al. 2018. Antiviral activity of bone morphogenetic proteins and activins. Nature Microbiology 4, pp. 339-351. (10.1038/s41564-018-0301-9)
- Volpato, V. et al. 2018. Reproducibility of molecular phenotypes after long-term differentiation to uuman iPSC-derived neurons: a multi-site omics study. Stem Cell Reports 11(4), pp. 897-911. (10.1016/j.stemcr.2018.08.013)
- Yang, Y. et al. 2018. Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics 26(8), pp. 1202-1216. (10.1038/s41431-018-0150-2)
- Anttila, V. et al. 2018. Analysis of shared heritability in common disorders of the brain. Science 360(6395), article number: eaap8757. (10.1126/science.aap8757)
- Sandor, C., Beer, N. L. and Webber, C. 2017. Diverse type 2 diabetes genetic risk factors functionally converge in a phenotype-focused gene network. PLoS Computational Biology 13(10), article number: e1005816. (10.1371/journal.pcbi.1005816)
- Sandor, C. et al. 2017. Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease. Human Molecular Genetics 26(3), pp. 552-566. (10.1093/hmg/ddw412)
- Sandor, C. et al. 2017. Whole-exome sequencing of 228 patients with sporadic Parkinson's disease. Scientific Reports 7, article number: 41188. (10.1038/srep41188)
- Gormley, P. et al. 2016. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48(10), pp. 1296. (10.1038/ng1016-1296c)
- Gormley, P. et al. 2016. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48(8), pp. 856-866. (10.1038/ng.3598)
- Eyre, S. et al. 2012. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics 44(12), pp. 1336-1340. (10.1038/ng.2462)