Marcy E. MacDonald, Ph.D.
Affiliations: | Neurology | Harvard Medical School, Boston, MA, United States |
Area:
Huntington's disease, NCLWebsite:
http://www2.massgeneral.org/chgr/faculty_macdonald.htmGoogle:
"Marcy MacDonald"Mean distance: 53433 (cluster 6)
Children
Sign in to add trainee| Christopher A. Korey | post-doc | 2001-2003 | Harvard Medical School and Department of Neurology |
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Publications
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| Hong EP, Ramos EM, Aziz NA, et al. (2024) Modification of Huntington's disease by short tandem repeats. Brain Communications. 6: fcae016 |
| Handley RR, Reid SJ, Burch Z, et al. (2024) Somatic CAG Repeat Stability in a Transgenic Sheep Model of Huntington's Disease. Journal of Huntington's Disease |
| McLean ZL, Gao D, Correia K, et al. (2023) as a target for splice modulation to prevent somatic CAG repeat expansion in Huntington's disease. Biorxiv : the Preprint Server For Biology |
| Lobanov SV, McAllister B, McDade-Kumar M, et al. (2022) Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. Npj Genomic Medicine. 7: 53 |
| McAllister B, Donaldson J, Binda CS, et al. (2022) Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience |
| Lee JM, Huang Y, Orth M, et al. (2022) Genetic modifiers of Huntington disease differentially influence motor and cognitive domains. American Journal of Human Genetics |
| Hong EP, Chao MJ, Massey T, et al. (2021) Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease |
| Hong EP, MacDonald ME, Wheeler VC, et al. (2021) Huntington's Disease Pathogenesis: Two Sequential Components. Journal of Huntington's Disease. 10: 35-51 |
| Loupe JM, Pinto RM, Kim KH, et al. (2020) Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out. Human Molecular Genetics |
| Kim KH, Hong EP, Shin JW, et al. (2020) Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects. American Journal of Human Genetics |