MacDonald ME - Search Results

1

Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease.

Ellis N, Tee A, McAllister B, Massey T, McLauchlan D, Stone T, Correia K, Loupe J, Kim KH, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, Pinto RM, Elneel KA, Ramos EM, Mysore JS, Gillis T, Wheeler VC, Medway C, Hall L, Kwak S, Sampaio C, Ciosi M, Maxwell A, Chatzi A, Monckton DG, Orth M, Landwehrmeyer GB, Paulsen JS, Shoulson I, Myers RH, van Duijn E, Rickards H, MacDonald ME, Lee JM, Gusella JF, Jones L, Holmans P. Ellis N, et al. Among authors: macdonald me. Biol Psychiatry. 2020 May 1;87(9):857-865. doi: 10.1016/j.biopsych.2019.12.010. Epub 2019 Dec 17. Biol Psychiatry. 2020. PMID: 32087949 Free PMC article.

2

The Huntington's disease candidate region exhibits many different haplotypes.

MacDonald ME, Novelletto A, Lin C, Tagle D, Barnes G, Bates G, Taylor S, Allitto B, Altherr M, Myers R, et al. MacDonald ME, et al. Nat Genet. 1992 May;1(2):99-103. doi: 10.1038/ng0592-99. Nat Genet. 1992. PMID: 1302016 Review.

3

A dinucleotide repeat polymorphism at the D4S127 locus.

Taylor SA, Barnes GT, MacDonald ME, Gusella JF. Taylor SA, et al. Among authors: macdonald me. Hum Mol Genet. 1992 May;1(2):142. doi: 10.1093/hmg/1.2.142-a. Hum Mol Genet. 1992. PMID: 1339471 No abstract available.

4

The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11.

Ambrose C, Cheng S, Fontaine B, Nadeau JH, MacDonald M, Gusella JF. Ambrose C, et al. Mamm Genome. 1992;3(3):151-5. doi: 10.1007/BF00352459. Mamm Genome. 1992. PMID: 1352160

5

A recombination event that redefines the Huntington disease region.

Snell RG, Thompson LM, Tagle DA, Holloway TL, Barnes G, Harley HG, Sandkuijl LA, MacDonald ME, Collins FS, Gusella JF, et al. Snell RG, et al. Among authors: macdonald me. Am J Hum Genet. 1992 Aug;51(2):357-62. Am J Hum Genet. 1992. PMID: 1386495 Free PMC article.

6

Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.

Allitto BA, McClatchey AI, Barnes G, Altherr M, Wasmuth J, Frischauf AM, MacDonald ME, Gusella J. Allitto BA, et al. Among authors: macdonald me. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

7

Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

Koizumi T, MacDonald M, Búcan M, Hopwood JJ, Morris CP, Scott HS, Gusella JF, Nadeau JH. Koizumi T, et al. Mamm Genome. 1992;3(1):23-7. doi: 10.1007/BF00355837. Mamm Genome. 1992. PMID: 1533802

8

Complex patterns of linkage disequilibrium in the Huntington disease region.

MacDonald ME, Lin C, Srinidhi L, Bates G, Altherr M, Whaley WL, Lehrach H, Wasmuth J, Gusella JF. MacDonald ME, et al. Am J Hum Genet. 1991 Oct;49(4):723-34. Am J Hum Genet. 1991. PMID: 1680285 Free PMC article.

9

MboI RFLP at the D4S43 (C4H) locus.

Lazarou LP, Snell RG, MacDonald ME, Gusella JF, Wasmuth JJ, Shaw DJ. Lazarou LP, et al. Among authors: macdonald me. Nucleic Acids Res. 1991 Oct 11;19(19):5445. doi: 10.1093/nar/19.19.5445-a. Nucleic Acids Res. 1991. PMID: 1681512 Free PMC article. No abstract available.

10

New DNA markers in the Huntington's disease gene candidate region.

Lin CS, Altherr M, Bates G, Whaley WL, Read AP, Harris R, Lehrach H, Wasmuth JJ, Gusella JF, MacDonald ME. Lin CS, et al. Among authors: macdonald me. Somat Cell Mol Genet. 1991 Sep;17(5):481-8. doi: 10.1007/BF01233172. Somat Cell Mol Genet. 1991. PMID: 1684879

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