Rubinsztein DC - Search Results

1

Apolipoprotein E4 is only a weak predictor of dementia and cognitive decline in the general population.

Yip AG, Brayne C, Easton D, Rubinsztein DC; Medical Research Council Cognitive Function Ageing Study (MRC CFAS). Yip AG, et al. Among authors: rubinsztein dc. J Med Genet. 2002 Sep;39(9):639-43. doi: 10.1136/jmg.39.9.639. J Med Genet. 2002. PMID: 12205106 Free PMC article.

2

The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.

Tysoe C, Robinson D, Brayne C, Dening T, Paykel ES, Huppert FA, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. J Med Genet. 1996 Dec;33(12):1002-6. doi: 10.1136/jmg.33.12.1002. J Med Genet. 1996. PMID: 9004131 Free PMC article.

3

Analysis of the apo E/apo C-I, angiotensin converting enzyme and methylenetetrahydrofolate reductase genes as candidates affecting human longevity.

Galinsky D, Tysoe C, Brayne CE, Easton DF, Huppert FA, Dening TR, Paykel ES, Rubinsztein DC. Galinsky D, et al. Among authors: rubinsztein dc. Atherosclerosis. 1997 Mar 21;129(2):177-83. doi: 10.1016/s0021-9150(96)06027-3. Atherosclerosis. 1997. PMID: 9105559

4

Analysis of alpha-1 antichymotrypsin, presenilin-1, angiotensin-converting enzyme, and methylenetetrahydrofolate reductase loci as candidates for dementia.

Tysoe C, Galinsky D, Robinson D, Brayne CE, Easton DF, Huppert FA, Dening T, Paykel ES, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. Am J Med Genet. 1997 Apr 18;74(2):207-12. doi: 10.1002/(sici)1096-8628(19970418)74:2<207::aid-ajmg20>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9129727

5

Mild myotonic dystrophy is associated with memory impairment in the context of normal general intelligence.

Rubinsztein JS, Rubinsztein DC, McKenna PJ, Goodburn S, Holland AJ. Rubinsztein JS, et al. Among authors: rubinsztein dc. J Med Genet. 1997 Mar;34(3):229-33. doi: 10.1136/jmg.34.3.229. J Med Genet. 1997. PMID: 9132495 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: rubinsztein dc. 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

Analysis and meta-analysis of two serotonin transporter gene polymorphisms in bipolar and unipolar affective disorders.

Furlong RA, Ho L, Walsh C, Rubinsztein JS, Jain S, Paykel ES, Easton DF, Rubinsztein DC. Furlong RA, et al. Among authors: rubinsztein dc, rubinsztein js. Am J Med Genet. 1998 Feb 7;81(1):58-63. Am J Med Genet. 1998. PMID: 9514589

8

No association of the tryptophan hydroxylase gene with bipolar affective disorder, unipolar affective disorder, or suicidal behaviour in major affective disorder.

Furlong RA, Ho L, Rubinsztein JS, Walsh C, Paykel ES, Rubinsztein DC. Furlong RA, et al. Among authors: rubinsztein dc, rubinsztein js. Am J Med Genet. 1998 May 8;81(3):245-7. Am J Med Genet. 1998. PMID: 9603613

9

Apo E and Apo CI loci are associated with dementia in younger but not older late-onset cases.

Tysoe C, Galinsky D, Robinson D, Brayne C, Huppert FA, Dening T, Paykel ES, Easton DF, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. Dement Geriatr Cogn Disord. 1998 Jul-Aug;9(4):191-8. doi: 10.1159/000017046. Dement Geriatr Cogn Disord. 1998. PMID: 9681640

10

No association of a functional polymorphism in the dopamine D2 receptor promoter region with bipolar or unipolar affective disorders.

Furlong RA, Coleman TA, Ho L, Rubinsztein JS, Walsh C, Paykel ES, Rubinsztein DC. Furlong RA, et al. Among authors: rubinsztein dc, rubinsztein js. Am J Med Genet. 1998 Sep 7;81(5):385-7. Am J Med Genet. 1998. PMID: 9754623

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