Rubinsztein DC - Search Results

1

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease.

Rubinsztein DC, Hanlon CS, Irving RM, Goodburn S, Evans DG, Kellar-Wood H, Xuereb JH, Bandmann O, Harding AE. Rubinsztein DC, et al. Mol Cell Probes. 1994 Dec;8(6):519-25. doi: 10.1006/mcpr.1994.1073. Mol Cell Probes. 1994. PMID: 7700274

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. Am J Med Genet. 1995 Apr 24;60(2):109-10. doi: 10.1002/ajmg.1320600205. Am J Med Genet. 1995. PMID: 7485243

3

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. Nat Genet. 1995 Jul;10(3):337-43. doi: 10.1038/ng0795-337. Nat Genet. 1995. PMID: 7670473

4

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. Hum Mol Genet. 1995 Feb;4(2):203-6. doi: 10.1093/hmg/4.2.203. Hum Mol Genet. 1995. PMID: 7757068

5

Arginine residues at codons 112 and 158 in the apolipoprotein E gene correspond to the ancestral state in humans.

Hanlon CS, Rubinsztein DC. Hanlon CS, et al. Among authors: rubinsztein dc. Atherosclerosis. 1995 Jan 6;112(1):85-90. doi: 10.1016/0021-9150(94)05402-5. Atherosclerosis. 1995. PMID: 7772071

6

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. 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.

7

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. Nat Genet. 1994 Aug;7(4):525-30. doi: 10.1038/ng0894-525. Nat Genet. 1994. PMID: 7951324

8

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: rubinsztein dc. 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

9

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. Hum Mol Genet. 1996 Jun;5(6):779-82. doi: 10.1093/hmg/5.6.779. Hum Mol Genet. 1996. PMID: 8776592

10

Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease.

Rubinsztein DC, Leggo J, Chiano M, Dodge A, Norbury G, Rosser E, Craufurd D. Rubinsztein DC, et al. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3872-6. doi: 10.1073/pnas.94.8.3872. Proc Natl Acad Sci U S A. 1997. PMID: 9108071 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

450 results

Search Page

Filters