Orr HT - Search Results

1

The c-fos gene and early-onset familial Alzheimer's disease.

Bonnycastle LL, Yu CE, Wijsman EM, Orr HT, Patterson D, Clancy KP, Goddard KA, Alonso ME, Nemens E, White JA, et al. Bonnycastle LL, et al. Among authors: orr ht. Neurosci Lett. 1993 Sep 17;160(1):33-6. doi: 10.1016/0304-3940(93)90910-d. Neurosci Lett. 1993. PMID: 8247328

2

The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

Yu CE, Payami H, Olson JM, Boehnke M, Wijsman EM, Orr HT, Kukull WA, Goddard KA, Nemens E, White JA, et al. Yu CE, et al. Among authors: orr ht. Am J Hum Genet. 1994 Apr;54(4):631-42. Am J Hum Genet. 1994. PMID: 8128960 Free PMC article.

3

Chromosome 14 and late-onset familial Alzheimer disease (FAD).

Schellenberg GD, Payami H, Wijsman EM, Orr HT, Goddard KA, Anderson L, Nemens E, White JA, Alonso ME, Ball MJ, et al. Schellenberg GD, et al. Among authors: orr ht. Am J Hum Genet. 1993 Sep;53(3):619-28. Am J Hum Genet. 1993. PMID: 8352272 Free PMC article.

4

Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.

Kamino K, Orr HT, Payami H, Wijsman EM, Alonso ME, Pulst SM, Anderson L, O'dahl S, Nemens E, White JA, et al. Kamino K, et al. Among authors: orr ht. Am J Hum Genet. 1992 Nov;51(5):998-1014. Am J Hum Genet. 1992. PMID: 1415269 Free PMC article.

5

Linkage of an Alzheimer disease susceptibility locus to markers on human chromosome 21.

Heston LL, Orr HT, Rich SS, White JA. Heston LL, et al. Among authors: orr ht. Am J Med Genet. 1991 Sep 15;40(4):449-53. doi: 10.1002/ajmg.1320400415. Am J Med Genet. 1991. PMID: 1684090

6

Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.

Schellenberg GD, Bird TD, Wijsman EM, Orr HT, Anderson L, Nemens E, White JA, Bonnycastle L, Weber JL, Alonso ME, et al. Schellenberg GD, et al. Among authors: orr ht. Science. 1992 Oct 23;258(5082):668-71. doi: 10.1126/science.1411576. Science. 1992. PMID: 1411576

7

The HLA class I gene family includes at least six genes and twelve pseudogenes and gene fragments.

Geraghty DE, Koller BH, Hansen JA, Orr HT. Geraghty DE, et al. Among authors: orr ht. J Immunol. 1992 Sep 15;149(6):1934-46. J Immunol. 1992. PMID: 1517563

8

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

9

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

10

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.

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