Ross OA - Search Results

1

Epigenetic regulation in Parkinson's disease.

Labbé C, Lorenzo-Betancor O, Ross OA. Labbé C, et al. Among authors: ross oa. Acta Neuropathol. 2016 Oct;132(4):515-30. doi: 10.1007/s00401-016-1590-9. Epub 2016 Jun 29. Acta Neuropathol. 2016. PMID: 27358065 Free PMC article. Review.

2

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.

3

LRRK2 mutations are a common cause of Parkinson's disease in Spain.

Mata IF, Ross OA, Kachergus J, Huerta C, Ribacoba R, Moris G, Blazquez M, Guisasola LM, Salvador C, Martinez C, Farrer M, Alvarez V. Mata IF, et al. Among authors: ross oa. Eur J Neurol. 2006 Apr;13(4):391-4. doi: 10.1111/j.1468-1331.2006.01256.x. Eur J Neurol. 2006. PMID: 16643318

4

Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.

Dächsel JC, Ross OA, Mata IF, Kachergus J, Toft M, Cannon A, Baker M, Adamson J, Hutton M, Dickson DW, Farrer MJ. Dächsel JC, et al. Among authors: ross oa. Acta Neuropathol. 2007 May;113(5):601-6. doi: 10.1007/s00401-006-0178-1. Epub 2006 Dec 7. Acta Neuropathol. 2007. PMID: 17151837

5

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.

Toft M, Mata IF, Ross OA, Kachergus J, Hulihan MM, Haugarvoll K, Stone JT, Blazquez M, Gibson JM, Aasly JO, White LR, Lynch T, Adler CH, Gwinn-Hardy K, Farrer MJ. Toft M, et al. Among authors: ross oa. Mov Disord. 2007 Feb 15;22(3):389-92. doi: 10.1002/mds.21217. Mov Disord. 2007. PMID: 17216639

6

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.

Farrer MJ, Stone JT, Lin CH, Dächsel JC, Hulihan MM, Haugarvoll K, Ross OA, Wu RM. Farrer MJ, et al. Among authors: ross oa. Parkinsonism Relat Disord. 2007 Mar;13(2):89-92. doi: 10.1016/j.parkreldis.2006.12.001. Epub 2007 Jan 10. Parkinsonism Relat Disord. 2007. PMID: 17222580

7

Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease.

Taylor JP, Hulihan MM, Kachergus JM, Melrose HL, Lincoln SJ, Hinkle KM, Stone JT, Ross OA, Hauser R, Aasly J, Gasser T, Payami H, Wszolek ZK, Farrer MJ. Taylor JP, et al. Among authors: ross oa. Neurogenetics. 2007 Apr;8(2):95-102. doi: 10.1007/s10048-006-0075-8. Epub 2007 Jan 16. Neurogenetics. 2007. PMID: 17225181

8

Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway.

Haugarvoll K, Toft M, Ross OA, White LR, Aasly JO, Farrer MJ. Haugarvoll K, et al. Among authors: ross oa. Neurosci Lett. 2007 Apr 18;416(3):299-301. doi: 10.1016/j.neulet.2007.02.020. Epub 2007 Feb 12. Neurosci Lett. 2007. PMID: 17324517

9

Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease.

Ross OA, Haugarvoll K, Stone JT, Heckman MG, White LR, Aasly JO, Mark Gibson J, Lynch T, Wszolek ZK, Uitti RJ, Farrer MJ. Ross OA, et al. Parkinsonism Relat Disord. 2007 Oct;13(7):386-8. doi: 10.1016/j.parkreldis.2007.01.010. Epub 2007 Apr 2. Parkinsonism Relat Disord. 2007. PMID: 17400506 Free PMC article.

10

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.

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