Hardy JA - Search Results

1

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, Biernacka JM, Brice A, DeStefano AL, Do CB, Eriksson N, Factor SA, Farrer MJ, Foroud T, Gasser T, Hamza T, Hardy JA, Heutink P, Hill-Burns EM, Klein C, Latourelle JC, Maraganore DM, Martin ER, Martinez M, Myers RH, Nalls MA, Pankratz N, Payami H, Satake W, Scott WK, Sharma M, Singleton AB, Stefansson K, Toda T, Tung JY, Vance J, Wood NW, Zabetian CP; 23andMe Genetic Epidemiology of Parkinson's Disease Consortium; International Parkinson's Disease Genomics Consortium; Parkinson's Disease GWAS Consortium; Wellcome Trust Case Control Consortium 2); Young P, Tanzi RE, Khoury MJ, Zipp F, Lehrach H, Ioannidis JP, Bertram L. Lill CM, et al. Among authors: hardy ja. PLoS Genet. 2012;8(3):e1002548. doi: 10.1371/journal.pgen.1002548. Epub 2012 Mar 15. PLoS Genet. 2012. PMID: 22438815 Free PMC article.

2

Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease.

Maraganore DM, Farrer MJ, Hardy JA, Lincoln SJ, McDonnell SK, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Neurology. 1999 Nov 10;53(8):1858-60. doi: 10.1212/wnl.53.8.1858. Neurology. 1999. PMID: 10563640

3

Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease.

Maraganore DM, Farrer MJ, Hardy JA, McDonnell SK, Schaid DJ, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Mov Disord. 2000 Jul;15(4):714-9. doi: 10.1002/1531-8257(200007)15:4<714::aid-mds1018>3.0.co;2-3. Mov Disord. 2000. PMID: 10928584

4

Case-Control study of the extended tau gene haplotype in Parkinson's disease.

Maraganore DM, Hernandez DG, Singleton AB, Farrer MJ, McDonnell SK, Hutton ML, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Ann Neurol. 2001 Nov;50(5):658-61. doi: 10.1002/ana.1228. Ann Neurol. 2001. PMID: 11706972

5

Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease.

Maraganore DM, Farrer MJ, McDonnell SK, Elbaz A, Schaid DJ, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Mov Disord. 2002 May;17(3):509-12. doi: 10.1002/mds.1253. Mov Disord. 2002. PMID: 12112198

6

Functional association of the parkin gene promoter with idiopathic Parkinson's disease.

West AB, Maraganore D, Crook J, Lesnick T, Lockhart PJ, Wilkes KM, Kapatos G, Hardy JA, Farrer MJ. West AB, et al. Among authors: hardy ja. Hum Mol Genet. 2002 Oct 15;11(22):2787-92. doi: 10.1093/hmg/11.22.2787. Hum Mol Genet. 2002. PMID: 12374768

7

Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.

Goudreau JL, Maraganore DM, Farrer MJ, Lesnick TG, Singleton AB, Bower JH, Hardy JA, Rocca WA. Goudreau JL, et al. Among authors: hardy ja. Mov Disord. 2002 Nov;17(6):1305-11. doi: 10.1002/mds.10268. Mov Disord. 2002. PMID: 12465073

8

Complex interactions in Parkinson's disease: a two-phased approach.

Maraganore DM, de Andrade M, Lesnick TG, Farrer MJ, Bower JH, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Mov Disord. 2003 Jun;18(6):631-6. doi: 10.1002/mds.10431. Mov Disord. 2003. PMID: 12784265

9

Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease.

Morris CM, O'Brien KK, Gibson AM, Hardy JA, Singleton AB. Morris CM, et al. Among authors: hardy ja. Neurosci Lett. 2003 Dec 4;352(2):151-3. doi: 10.1016/j.neulet.2003.08.037. Neurosci Lett. 2003. PMID: 14625045

10

Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease.

Maraganore DM, Farrer MJ, Lesnick TG, de Andrade M, Bower JH, Hernandez D, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: hardy ja. Mov Disord. 2003 Nov;18(11):1233-9. doi: 10.1002/mds.10547. Mov Disord. 2003. PMID: 14639662

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