Harold T. Orr, Ph.D.

Affiliations: 
Institute of Human Genetics University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Neurodegenerative disorders
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"Harold Orr"
Mean distance: 106866 (cluster 11)
 
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Publications

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Cvetanovic M, Ingram M, Orr H, et al. (2015) Early activation of microglia and astrocytes in mouse models of spinocerebellar ataxia type 1. Neuroscience. 289: 289-99
Lasagna-Reeves CA, Rousseaux MWC, Guerrero-Munoz MJ, et al. (2015) A native interactor scaffolds and stabilizes toxic Ataxin-1 oligomers in SCA1 Elife. 4: 1-46
Hardy J, Orr H. (2006) The genetics of neurodegenerative diseases Journal of Neurochemistry. 97: 1690-1699
Fernandez-Funez P, Nino-Rosales ML, de Gouyon B, et al. (2000) Identification of genes that modify ataxin-1-induced neurodegeneration. Nature. 408: 101-6
Johnson EW, Dubovsky J, Rich SS, et al. (1998) Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest. Human Molecular Genetics. 7: 63-7
Gil-Nagel A, Dubovsky J, Wilcox KJ, et al. (1996) Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q. Annals of Neurology. 39: 807-10
Johnson EW, Iyer LM, Rich SS, et al. (1995) Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. Genome Research. 5: 368-80
Yu CE, Payami H, Olson JM, et al. (1994) The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease. American Journal of Human Genetics. 54: 631-42
Ranum LPW, Chung MY, Banfi S, et al. (1994) Molecular and clinical correlations in spinocerebellar ataxia type I: Evidence for familial effects on the age at onset American Journal of Human Genetics. 55: 244-252
Schellenberg GD, Payami H, Wijsman EM, et al. (1993) Chromosome 14 and late-onset familial Alzheimer disease (FAD). American Journal of Human Genetics. 53: 619-28
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