Ross OA - Search Results

1

Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease.

Ross OA, Gosal D, Stone JT, Lincoln SJ, Heckman MG, Irvine GB, Johnston JA, Gibson JM, Farrer MJ, Lynch T. Ross OA, et al. Mech Ageing Dev. 2007 May-Jun;128(5-6):378-82. doi: 10.1016/j.mad.2007.04.002. Epub 2007 Apr 24. Mech Ageing Dev. 2007. PMID: 17531291 Free PMC article.

2

A novel polymorphic triplet repeat in intron five of the alpha-synuclein gene: no evidence of expansion or allelic association with idiopathic Parkinson's disease in the Irish.

Ross OA, Awayn NH, McWhinney D, Maxwell LD, El-Agnaf OM, Barnett YA, Rea IM, Middleton D, Wallace A, Gibson JM, Curran MD. Ross OA, et al. Neuroreport. 2002 Sep 16;13(13):1621-5. doi: 10.1097/00001756-200209160-00010. Neuroreport. 2002. PMID: 12352614

3

mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish.

Ross OA, McCormack R, Maxwell LD, Duguid RA, Quinn DJ, Barnett YA, Rea IM, El-Agnaf OM, Gibson JM, Wallace A, Middleton D, Curran MD. Ross OA, et al. Exp Gerontol. 2003 Apr;38(4):397-405. doi: 10.1016/s0531-5565(02)00266-8. Exp Gerontol. 2003. PMID: 12670626

4

HLA haplotypes and TNF polymorphism do not associate with longevity in the Irish.

Ross OA, Curran MD, Rea IM, Hyland P, Duggan O, Barnett CR, Annett K, Patterson C, Barnett YA, Middleton D. Ross OA, et al. Mech Ageing Dev. 2003 Apr;124(4):563-7. doi: 10.1016/s0047-6374(03)00037-x. Mech Ageing Dev. 2003. PMID: 12714268

5

Functional promoter region polymorphism of the proinflammatory chemokine IL-8 gene associates with Parkinson's disease in the Irish.

Ross OA, O'Neill C, Rea IM, Lynch T, Gosal D, Wallace A, Curran MD, Middleton D, Gibson JM. Ross OA, et al. Hum Immunol. 2004 Apr;65(4):340-6. doi: 10.1016/j.humimm.2004.01.015. Hum Immunol. 2004. PMID: 15120188

6

Linkage disequilibrium and association of MAPT H1 in Parkinson disease.

Skipper L, Wilkes K, Toft M, Baker M, Lincoln S, Hulihan M, Ross OA, Hutton M, Aasly J, Farrer M. Skipper L, et al. Among authors: ross oa. Am J Hum Genet. 2004 Oct;75(4):669-77. doi: 10.1086/424492. Epub 2004 Aug 3. Am J Hum Genet. 2004. PMID: 15297935 Free PMC article.

7

PINK1 (PARK6) associated Parkinson disease in Ireland.

Healy DG, Abou-Sleiman PM, Gibson JM, Ross OA, Jain S, Gandhi S, Gosal D, Muqit MM, Wood NW, Lynch T. Healy DG, et al. Among authors: ross oa. Neurology. 2004 Oct 26;63(8):1486-8. doi: 10.1212/01.wnl.0000142089.38301.8e. Neurology. 2004. PMID: 15505171

8

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M. Kachergus J, et al. Among authors: ross oa. Am J Hum Genet. 2005 Apr;76(4):672-80. doi: 10.1086/429256. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726496 Free PMC article.

9

LRRK2 mutations and Parkinsonism.

Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ. Toft M, et al. Among authors: ross oa. Lancet. 2005 Apr 2-8;365(9466):1229-30. doi: 10.1016/S0140-6736(05)74809-1. Lancet. 2005. PMID: 15811454 No abstract available.

10

Pathophysiology, pleiotrophy and paradigm shifts: genetic lessons from Parkinson's disease.

Ross OA, Farrer MJ. Ross OA, et al. Biochem Soc Trans. 2005 Aug;33(Pt 4):586-90. doi: 10.1042/BST0330586. Biochem Soc Trans. 2005. PMID: 16042550 Review.

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