Ross, Olivia A.

Publishing since 2002 (Junior)

Has published 11 publications in 8 years

Number of publications published per year by Ross, Olivia A.. (Source : PubMed)

Distribution of publications types for Ross, Olivia A.. (Source : PubMed)
(a publication can be of different types, so total may exceed publications count)

Recent publications

•  Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, Aasly JO, Farrer MJ. Fine-mapping and candidate gene investigation within the PARK10 locus.  Eur. J. Hum. Genet.  2009;17;3  
•  Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK. DCTN1 mutations in Perry syndrome.  Nat. Genet.  2009;41;2  
•  Watt AP, Ross OA, Courtney J, Middleton D, Ennis M, Elborn JS. Frequency of cytokine gene promoter polymorphisms in the Northern Ireland cystic fibrosis population.  J. Cyst. Fibros.  2007;6;5  
•  Ross OA, Worrall BB, Meschia JF. Advancing stroke therapeutics through genetic understanding.  Curr Drug Targets  2007;8;7  
•  Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M. Genomewide association, Parkinson disease, and PARK10.  Am. J. Hum. Genet.  2006;78;6  
•  Ross OA. Longevics: genetic lessons for the ages.  Ir J Med Sci  2006;175;1  
•  Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ. LRRK2 mutations and Parkinsonism.  Lancet  2005;365;9466  
•  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. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.  Am. J. Hum. Genet.  2005;76;4  
•  Skipper L, Wilkes K, Toft M, Baker M, Lincoln S, Hulihan M, Ross OA, Hutton M, Aasly J, Farrer M. Linkage disequilibrium and association of MAPT H1 in Parkinson disease.  Am. J. Hum. Genet.  2004;75;4  
•  Ross OA, O'Neill C, Rea IM, Lynch T, Gosal D, Wallace A, Curran MD, Middleton D, Gibson JM. Functional promoter region polymorphism of the proinflammatory chemokine IL-8 gene associates with Parkinson's disease in the Irish.  Hum. Immunol.  2004;65;4  

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