Gusella JF - Search Results

1

Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease.

Hong EP, Chao MJ, Massey T, McAllister B, Lobanov S, Jones L, Holmans P, Kwak S, Orth M, Ciosi M, Monckton DG, Long JD, Lucente D, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. Hong EP, et al. Among authors: gusella jf. J Huntingtons Dis. 2021;10(3):367-375. doi: 10.3233/JHD-210485. J Huntingtons Dis. 2021. PMID: 34180418 Free PMC article.

2

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. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

3

Trinucleotide repeat length and progression of illness in Huntington's disease.

Kieburtz K, MacDonald M, Shih C, Feigin A, Steinberg K, Bordwell K, Zimmerman C, Srinidhi J, Sotack J, Gusella J, et al. Kieburtz K, et al. J Med Genet. 1994 Nov;31(11):872-4. doi: 10.1136/jmg.31.11.872. J Med Genet. 1994. PMID: 7853373 Free PMC article.

4

High resolution localization of recombination hot spots using sperm typing.

Hubert R, MacDonald M, Gusella J, Arnheim N. Hubert R, et al. Nat Genet. 1994 Jul;7(3):420-4. doi: 10.1038/ng0794-420. Nat Genet. 1994. PMID: 7920662

5

Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22.

MacCollin M, Peterfreund R, MacDonald M, Fink JS, Gusella J. MacCollin M, et al. Genomics. 1994 Mar 15;20(2):332-3. doi: 10.1006/geno.1994.1181. Genomics. 1994. PMID: 8020991 No abstract available.

6

Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.

Hummerich H, Baxendale S, Mott R, Kirby SF, MacDonald ME, Gusella J, Lehrach H, Bates GP. Hummerich H, et al. Hum Mol Genet. 1994 Jan;3(1):73-8. doi: 10.1093/hmg/3.1.73. Hum Mol Genet. 1994. PMID: 8162055

7

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat.

Ambrose CM, Duyao MP, Barnes G, Bates GP, Lin CS, Srinidhi J, Baxendale S, Hummerich H, Lehrach H, Altherr M, Wasmuth J, Buckler A, Church D, Housman D, Berks M, Micklem G, Durbin R, Dodge A, Read A, Gusella J, MacDonald ME. Ambrose CM, et al. Somat Cell Mol Genet. 1994 Jan;20(1):27-38. doi: 10.1007/BF02257483. Somat Cell Mol Genet. 1994. PMID: 8197474

8

No post-genetics era in human disease research.

Gusella J, MacDonald M. Gusella J, et al. Nat Rev Genet. 2002 Jan;3(1):72-9. doi: 10.1038/nrg706. Nat Rev Genet. 2002. PMID: 11823793 Review.

9

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice.

Wheeler VC, Gutekunst CA, Vrbanac V, Lebel LA, Schilling G, Hersch S, Friedlander RM, Gusella JF, Vonsattel JP, Borchelt DR, MacDonald ME. Wheeler VC, et al. Among authors: gusella jf. Hum Mol Genet. 2002 Mar 15;11(6):633-40. doi: 10.1093/hmg/11.6.633. Hum Mol Genet. 2002. PMID: 11912178

10

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.

DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, Montgomery E, Waters CH, Singer C, Watts RL, Currie LJ, Wooten GF, Maher NE, Wilk JB, Sullivan KM, Slater KM, Saint-Hilaire MH, Feldman RG, Suchowersky O, Lafontaine AL, Labelle N, Growdon JH, Vieregge P, Pramstaller PP, Klein C, Hubble JP, Reider CR, Stacy M, MacDonald ME, Gusella JF, Myers RH. DeStefano AL, et al. Among authors: gusella jf. Am J Hum Genet. 2002 May;70(5):1089-95. doi: 10.1086/339814. Epub 2002 Mar 27. Am J Hum Genet. 2002. PMID: 11920285 Free PMC article.

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