Leggo J - Search Results

1

Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.

Leggo J, Dalton A, Morrison PJ, Dodge A, Connarty M, Kotze MJ, Rubinsztein DC. Leggo J, et al. J Med Genet. 1997 Dec;34(12):982-5. doi: 10.1136/jmg.34.12.982. J Med Genet. 1997. PMID: 9429138 Free PMC article.

2

Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patients.

Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Am J Med Genet. 1995 Apr 24;60(2):109-10. doi: 10.1002/ajmg.1320600205. Am J Med Genet. 1995. PMID: 7485243

3

Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes.

Rubinsztein DC, Leggo J, Coetzee GA, Irvine RA, Buckley M, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Hum Mol Genet. 1995 Sep;4(9):1585-90. doi: 10.1093/hmg/4.9.1585. Hum Mol Genet. 1995. PMID: 8541843

4

Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder.

Rubinsztein DC, Leggo J, Crow TJ, DeLisi LE, Walsh C, Jain S, Paykel ES. Rubinsztein DC, et al. Among authors: leggo j. Am J Med Genet. 1996 Sep 20;67(5):495-8. doi: 10.1002/(SICI)1096-8628(19960920)67:5<495::AID-AJMG12>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8886170

5

Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats.

Rubinsztein DC, Leggo J. Rubinsztein DC, et al. Among authors: leggo j. J Med Genet. 1997 Mar;34(3):234-6. doi: 10.1136/jmg.34.3.234. J Med Genet. 1997. PMID: 9132496 Free PMC article.

6

Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD.

Coles R, Leggo J, Rubinsztein DC. Coles R, et al. Among authors: leggo j. J Med Genet. 1997 May;34(5):371-4. doi: 10.1136/jmg.34.5.371. J Med Genet. 1997. PMID: 9152833 Free PMC article.

7

Microsatellite evolution--evidence for directionality and variation in rate between species.

Rubinsztein DC, Amos W, Leggo J, Goodburn S, Jain S, Li SH, Margolis RL, Ross CA, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Nat Genet. 1995 Jul;10(3):337-43. doi: 10.1038/ng0795-337. Nat Genet. 1995. PMID: 7670473

8

Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype.

Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Hum Mol Genet. 1995 Feb;4(2):203-6. doi: 10.1093/hmg/4.2.203. Hum Mol Genet. 1995. PMID: 7757068

9

Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.

Rubinsztein DC, Leggo J, Goodburn S, Crow TJ, Lofthouse R, DeLisi LE, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. J Med Genet. 1994 Sep;31(9):690-3. doi: 10.1136/jmg.31.9.690. J Med Genet. 1994. PMID: 7815437 Free PMC article.

10

Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.

Rubinsztein DC, Leggo J, Amos W, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Hum Mol Genet. 1994 Nov;3(11):2031-5. Hum Mol Genet. 1994. PMID: 7874122

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