Leggo J - Search Results

1

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.

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

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

4

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.

5

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

6

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

Rubinsztein DC, Amos W, Leggo J, Goodburn S, Ramesar RS, Old J, Bontrop R, McMahon R, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: leggo j. Nat Genet. 1994 Aug;7(4):525-30. doi: 10.1038/ng0894-525. Nat Genet. 1994. PMID: 7951324

7

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

8

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.

Rubinsztein DC, Leggo J, Coles R, Almqvist E, Biancalana V, Cassiman JJ, Chotai K, Connarty M, Crauford D, Curtis A, Curtis D, Davidson MJ, Differ AM, Dode C, Dodge A, Frontali M, Ranen NG, Stine OC, Sherr M, Abbott MH, Franz ML, Graham CA, Harper PS, Hedreen JC, Hayden MR, et al. Rubinsztein DC, et al. Among authors: leggo j. Am J Hum Genet. 1996 Jul;59(1):16-22. Am J Hum Genet. 1996. PMID: 8659522 Free PMC article.

9

Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder.

Jain S, Leggo J, DeLisi LE, Crow TJ, Margolis RL, Li SH, Goodburn S, Walsh C, Paykel ES, Ferguson-Smith MA, Ross CA, Rubinsztein DC. Jain S, et al. Among authors: leggo j. Am J Med Genet. 1996 Apr 9;67(2):139-46. doi: 10.1002/(SICI)1096-8628(19960409)67:2<139::AID-AJMG3>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723040

10

Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder: analysis and meta-analysis.

Rubinsztein DC, Leggo J, Goodburn S, Walsh C, Jain S, Paykel ES. Rubinsztein DC, et al. Among authors: leggo j. Hum Mol Genet. 1996 Jun;5(6):779-82. doi: 10.1093/hmg/5.6.779. Hum Mol Genet. 1996. PMID: 8776592

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