Orr HT - Search Results

1

Prioritized research recommendations from the National Institute of Neurological Disorders and Stroke Parkinson's Disease 2014 conference.

Sieber BA, Landis S, Koroshetz W, Bateman R, Siderowf A, Galpern WR, Dunlop J, Finkbeiner S, Sutherland M, Wang H, Lee VM, Orr HT, Gwinn K, Ludwig K, Taylor A, Torborg C, Montine TJ; Parkinson's Disease 2014: Advancing Research, Improving Lives Conference Organizing Committee. Sieber BA, et al. Among authors: orr ht. Ann Neurol. 2014 Oct;76(4):469-72. doi: 10.1002/ana.24261. Epub 2014 Sep 23. Ann Neurol. 2014. PMID: 25164235 Free PMC article. No abstract available.

2

Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q.

Gil-Nagel A, Dubovsky J, Wilcox KJ, Stewart JM, Anderson VE, Leppik IE, Orr HT, Johnson EW, Weber JL, Rich SS. Gil-Nagel A, et al. Among authors: orr ht. Ann Neurol. 1996 Jun;39(6):807-10. doi: 10.1002/ana.410390619. Ann Neurol. 1996. PMID: 8651655

3

Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.

Ranum LP, Rich SS, Nance MA, Duvick LA, Aita JF, Orr HT, Anton-Johnson S, Schut LJ. Ranum LP, et al. Among authors: orr ht. Neurology. 1992 Feb;42(2):344-7. doi: 10.1212/wnl.42.2.344. Neurology. 1992. PMID: 1736163

4

Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

Rich SS, Wilkie P, Schut L, Vance G, Orr HT. Rich SS, et al. Among authors: orr ht. Am J Hum Genet. 1987 Oct;41(4):524-31. Am J Hum Genet. 1987. PMID: 3477955 Free PMC article.

5

A gene responsible for cavernous malformations of the brain maps to chromosome 7q.

Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL. Dubovsky J, et al. Among authors: orr ht. Hum Mol Genet. 1995 Mar;4(3):453-8. doi: 10.1093/hmg/4.3.453. Hum Mol Genet. 1995. PMID: 7795602

6

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.

Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, Morrison LA, Green ED, Weber JL. Johnson EW, et al. Among authors: orr ht. Genome Res. 1995 Nov;5(4):368-80. doi: 10.1101/gr.5.4.368. Genome Res. 1995. PMID: 8750196 Free article.

7

Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.

Johnson EW, Dubovsky J, Rich SS, O'Donovan CA, Orr HT, Anderson VE, Gil-Nagel A, Ahmann P, Dokken CG, Schneider DT, Weber JL. Johnson EW, et al. Among authors: orr ht. Hum Mol Genet. 1998 Jan;7(1):63-7. doi: 10.1093/hmg/7.1.63. Hum Mol Genet. 1998. PMID: 9384604

8

A polymorphic DNA probe, p1-10-2, from chromosome 6.

Duvick L, Rich SS, Orr HT. Duvick L, et al. Among authors: orr ht. Nucleic Acids Res. 1990 May 25;18(10):3105. doi: 10.1093/nar/18.10.3105. Nucleic Acids Res. 1990. PMID: 1971928 Free PMC article.

9

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT. Ranum LP, et al. Among authors: orr ht. Am J Hum Genet. 1991 Jul;49(1):31-41. Am J Hum Genet. 1991. PMID: 1676561 Free PMC article.

10

Chromosomal organization of the human major histocompatibility complex class I gene family.

Koller BH, Geraghty DE, DeMars R, Duvick L, Rich SS, Orr HT. Koller BH, et al. Among authors: orr ht. J Exp Med. 1989 Feb 1;169(2):469-80. doi: 10.1084/jem.169.2.469. J Exp Med. 1989. PMID: 2562983 Free PMC article.

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