Biblio

Add Citation
Export 11 results:
Sort by: Author Title Type [ Year (Desc)]
Filters: Author is Hardy, John A  [Clear All Filters]
2009
Scholz SW, Houlden H, Schulte C, Sharma M, Li A, Berg D, et al. SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol. 2009;65(5):610-4.
2007
Matarín M, Brown MW, Scholz S, Simón-Sánchez J, Fung HC, Hernandez D, et al. A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet neurology. 2007;6(5):414-20.
2006
Fung HC, Scholz S, Matarin M, Simón-Sánchez J, Hernandez D, Britton A, et al. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol. 2006;5(11):911-6.
2004
Bandopadhyay R, Kingsbury AE, Cookson MR, Reid AR, Evans IM, Hope AD, et al. The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease. Brain. 2004;127(Pt 2):420-30.
2003
Lincoln SJ, Maraganore DM, Lesnick TG, Bounds R, de Andrade M, Bower JH, et al. Parkin variants in North American Parkinson's disease: cases and controls. Mov Disord. 2003;18(11):1306-11.
Maraganore DM, Farrer MJ, Lesnick TG, de Andrade M, Bower JH, Hernandez D, et al. Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease. Mov Disord. 2003;18(11):1233-9.
Maraganore DM, de Andrade M, Lesnick TG, Farrer MJ, Bower JH, Hardy JA, et al. Complex interactions in Parkinson's disease: a two-phased approach. Mov Disord. 2003;18(6):631-6.
Morris CM, O'Brien KK, Gibson AM, Hardy JA, Singleton AB. Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease. Neurosci Lett. 2003;352(2):151-3.
2002
West AB, Maraganore D, Crook J, Lesnick T, Lockhart PJ, Wilkes KM, et al. Functional association of the parkin gene promoter with idiopathic Parkinson's disease. Hum Mol Genet. 2002;11(22):2787-92.
Goudreau JL, Maraganore DM, Farrer MJ, Lesnick TG, Singleton AB, Bower JH, et al. Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease. Mov Disord. 2002;17(6):1305-11.
Maraganore DM, Farrer MJ, McDonnell SK, Elbaz A, Schaid DJ, Hardy JA, et al. Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease. Mov Disord. 2002;17(3):509-12.