Brookes AJ - Search Results

1

A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.

Mellick GD, Silburn PA, Prince JA, Brookes AJ. Mellick GD, et al. Among authors: brookes aj. J Neural Transm (Vienna). 2004 Feb;111(2):191-9. doi: 10.1007/s00702-003-0085-8. Epub 2003 Dec 12. J Neural Transm (Vienna). 2004. PMID: 14767722

2

Genetic association analysis: lessons from the study of Alzheimers disease.

Brookes AJ, Prince JA. Brookes AJ, et al. Mutat Res. 2005 Jun 3;573(1-2):152-9. doi: 10.1016/j.mrfmmm.2004.08.017. Mutat Res. 2005. PMID: 15829244 Review.

3

The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls.

Mellick GD, Buchanan DD, Hattori N, Brookes AJ, Mizuno Y, Le Couteur DG, Silburn PA. Mellick GD, et al. Among authors: brookes aj. Parkinsonism Relat Disord. 2001 Apr;7(2):89-91. doi: 10.1016/s1353-8020(00)00018-3. Parkinsonism Relat Disord. 2001. PMID: 11248588

4

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

Blomqvist ME, Silburn PA, Buchanan DD, Andreasen N, Blennow K, Pedersen NL, Brookes AJ, Mellick GD, Prince JA. Blomqvist ME, et al. Among authors: brookes aj. Neurogenetics. 2004 Jun;5(2):115-9. doi: 10.1007/s10048-004-0173-4. Epub 2004 Apr 16. Neurogenetics. 2004. PMID: 15088150

5

No association between the alpha2-macroglobulin (A2M) deletion and Alzheimer's disease, and no change in A2M mRNA, protein, or protein expression.

Blennow K, Ricksten A, Prince JA, Brookes AJ, Emahazion T, Wasslavik C, Bogdanovic N, Andreasen N, Båtsman S, Marcusson J, Nägga K, Wallin A, Regland B, Olofsson H, Hesse C, Davidsson P, Minthon L, Jansson A, Palmqvist L, Rymo L. Blennow K, et al. Among authors: brookes aj. J Neural Transm (Vienna). 2000;107(8-9):1065-79. doi: 10.1007/s007020070052. J Neural Transm (Vienna). 2000. PMID: 11041282

6

Towards high-throughput genotyping of SNPs by dynamic allele-specific hybridization.

Prince JA, Brookes AJ. Prince JA, et al. Among authors: brookes aj. Expert Rev Mol Diagn. 2001 Sep;1(3):352-8. doi: 10.1586/14737159.1.3.352. Expert Rev Mol Diagn. 2001. PMID: 11901841

7

Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease.

Prince JA, Feuk L, Sawyer SL, Gottfries J, Ricksten A, Nägga K, Bogdanovic N, Blennow K, Brookes AJ. Prince JA, et al. Among authors: brookes aj. Eur J Hum Genet. 2001 Jun;9(6):437-44. doi: 10.1038/sj.ejhg.5200651. Eur J Hum Genet. 2001. PMID: 11436125

8

Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's disease.

Feuk L, McCarthy S, Andersson B, Prince JA, Brookes AJ. Feuk L, et al. Among authors: brookes aj. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):69-71. doi: 10.1002/ajmg.b.30172. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15858821

9

Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer disease.

Feuk L, Prince JA, Blennow K, Brookes AJ. Feuk L, et al. Among authors: brookes aj. Hum Mutat. 2003 Jan;21(1):53-60. doi: 10.1002/humu.10148. Hum Mutat. 2003. PMID: 12497631

10

Haplotypes extending across ACE are associated with Alzheimer's disease.

Kehoe PG, Katzov H, Feuk L, Bennet AM, Johansson B, Wiman B, de Faire U, Cairns NJ, Wilcock GK, Brookes AJ, Blennow K, Prince JA. Kehoe PG, et al. Among authors: brookes aj. Hum Mol Genet. 2003 Apr 15;12(8):859-67. doi: 10.1093/hmg/ddg094. Hum Mol Genet. 2003. PMID: 12668609

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