Huntington Disease

Displaying 1 - 13 of 13CSV
Paryani, F., Kwon, J.-S., Ng, C. W., Jakubiak, K., Madden, N., Ofori, K., Tang, A., Lu, H., Xia, S., Li, J., Mahajan, A., Davidson, S. M., Basile, A. O., McHugh, C., Vonsattel, J. P., Hickman, R., Zody, M. C., Housman, D. E., Goldman, J. E., … Al-Dalahmah, O. (2024). Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-50626-0
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Li, H., Desai, R., Quiles, N., Quinn, L., & Friel, C. (2024). Characterizing Heart Rate Variability Response to Maximal Exercise Testing in People with Huntington’s Disease. Journal of Huntington’s Disease, 13(1), 67–76. https://doi.org/10.3233/jhd-230593
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Goldman, J. S., Uhlmann, W. R., Naini, A. B., Klitzman, R. L., & Marder, K. S. (2023). Genetic Testing of HTT Modifiers for Huntington’s Disease: Considerations for Clinical Guidelines. Movement Disorders, 38(12), 2151–2154. Portico. https://doi.org/10.1002/mds.29650
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Shih, H.-J. S., Quinn, L., Morgan-Jones, P., Long, K., Schreier, A. R., & Friel, C. P. (2023). Wearable Activity Monitors to Support Physical Activity Interventions in Neurodegenerative Disease: A Feasibility Study. Neurodegenerative Disease Management, 13(3), 177–189. https://doi.org/10.2217/nmt-2022-0028
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Song, S., Su, Z., Kon, N., Chu, B., Li, H., Jiang, X., Luo, J., Stockwell, B. R., & Gu, W. (2023). ALOX5-mediated ferroptosis acts as a distinct cell death pathway upon oxidative stress in Huntington’s disease. Genes & Development, 37(5–6), 204–217. https://doi.org/10.1101/gad.350211.122
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Pepe, G., Capocci, L., Marracino, F., Realini, N., Lenzi, P., Martinello, K., Bovier, T. F., Bichell, T. J., Scarselli, P., Di Cicco, C., Bowman, A. B., Digilio, F. A., Fucile, S., Fornai, F., Armirotti, A., Parlato, R., Di Pardo, A., & Maglione, V. (2023). Treatment with THI, an inhibitor of sphingosine-1-phosphate lyase, modulates glycosphingolipid metabolism and results therapeutically effective in experimental models of Huntington’s disease. Molecular Therapy, 31(1), 282–299. https://doi.org/10.1016/j.ymthe.2022.09.004
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Lim, R. G., Al-Dalahmah, O., Wu, J., Gold, M. P., Reidling, J. C., Tang, G., Adam, M., Dansu, D. K., Park, H.-J., Casaccia, P., Miramontes, R., Reyes-Ortiz, A. M., Lau, A., Hickman, R. A., Khan, F., Paryani, F., Tang, A., Ofori, K., Miyoshi, E., … Thompson, L. M. (2022). Huntington disease oligodendrocyte maturation deficits revealed by single-nucleus RNAseq are rescued by thiamine-biotin supplementation. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-35388-x
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Hickman, R. A., Faust, P. L., Marder, K., Yamamoto, A., & Vonsattel, J.-P. (2022). The distribution and density of Huntingtin inclusions across the Huntington disease neocortex: regional correlations with Huntingtin repeat expansion independent of pathologic grade. Acta Neuropathologica Communications, 10(1). https://doi.org/10.1186/s40478-022-01364-1
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Quinn, L., Playle, R., Drew, C. J. G., Taiyari, K., Williams-Thomas, R., Muratori, L. M., Hamana, K., Griffin, B. A., Kelson, M., Schubert, R., Friel, C., Morgan-Jones, P., Rosser, A., Busse, M., Montojo, T., Ruiz Idiago, J. M., Hershberg, J., Marder, K., Bordelon, Y., … Landwehrmeyer, B. (2022). Physical activity and exercise outcomes in Huntington’s disease (PACE-HD): results of a 12-month trial-within-cohort feasibility study of a physical activity intervention in people with Huntington’s disease. Parkinsonism & Related Disorders, 101, 75–89. https://doi.org/10.1016/j.parkreldis.2022.06.013
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Fritz, N. E., Busse, M., Muratori, L. M., Rao, A. K., Kloos, A., Kegelmeyer, D., & Quinn, L. (2022). An MDS Evidence‐Based Review on Treatments for Huntington’s Disease. Movement Disorders, 37(7), 1566–1567. Portico. https://doi.org/10.1002/mds.29059
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Xie, S., McDonnell, E., & Wang, Y. (2021). Conditional Gaussian graphical model for estimating personalized disease symptom networks. Statistics in Medicine, 41(3), 543–553. Portico. https://doi.org/10.1002/sim.9274
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